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Volumn 9, Issue 1, 2018, Pages 47-62

Glycosylation engineering of therapeutic IgG antibodies: challenges for the safety, functionality and efficacy

Author keywords

chemoenzymatic glycoengineering; crystal structure; endoglycosidase; fucose; glycosylation; intravenous immunoglobulin; sialic acid; transglycosylation; ultra performance liquid chromatography

Indexed keywords

BEVACIZUMAB; CETUXIMAB; CLAZAKIZUMAB; FC RECEPTOR; FUCOSE; GALACTOSE; GLYCAN; IMMUNOGLOBULIN G ANTIBODY; MOGAMULIZUMAB; N ACETYL BETA GLUCOSAMINIDASE; NIVOLUMAB; OBINUTUZUMAB; ONARTUZUMAB; OTELIXIZUMAB; OXAZOLINE DERIVATIVE; SIALIC ACID; IMMUNOGLOBULIN G; MONOCLONAL ANTIBODY;

EID: 85020404761     PISSN: 1674800X     EISSN: 16748018     Source Type: Journal    
DOI: 10.1007/s13238-017-0433-3     Document Type: Review
Times cited : (155)

References (136)
  • 2
    • 54449089342 scopus 로고    scopus 로고
    • In vivo enzymatic modulation of IgG glycosylation inhibits autoimmune disease in an IgG subclass-dependent manner
    • COI: 1:CAS:528:DC%2BD1cXht1aqurzL, PID: 18815375
    • Albert H, Collin M, Dudziak D, Ravetch JV, Nimmerjahn F (2008) In vivo enzymatic modulation of IgG glycosylation inhibits autoimmune disease in an IgG subclass-dependent manner. Proc Natl Acad Sci USA 105:15005–15009
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 15005-15009
    • Albert, H.1    Collin, M.2    Dudziak, D.3    Ravetch, J.V.4    Nimmerjahn, F.5
  • 3
    • 69949159693 scopus 로고    scopus 로고
    • Sugar-free antibodies—the bacterial solution to autoimmunity?
    • COI: 1:CAS:528:DC%2BD1MXhtlCnt7%2FL, PID: 19758213
    • Allhorn M, Collin M (2009) Sugar-free antibodies—the bacterial solution to autoimmunity? Ann N Y Acad Sci 1173:664–669
    • (2009) Ann N Y Acad Sci , vol.1173 , pp. 664-669
    • Allhorn, M.1    Collin, M.2
  • 4
    • 79960046406 scopus 로고    scopus 로고
    • Intravenous gammaglobulin suppresses inflammation through a novel T(H)2 pathway
    • COI: 1:CAS:528:DC%2BC3MXnslSlu74%3D, PID: 21685887
    • Anthony RM, Kobayashi T, Wermeling F, Ravetch JV (2011) Intravenous gammaglobulin suppresses inflammation through a novel T(H)2 pathway. Nature 475:110–113
    • (2011) Nature , vol.475 , pp. 110-113
    • Anthony, R.M.1    Kobayashi, T.2    Wermeling, F.3    Ravetch, J.V.4
  • 5
    • 42349085035 scopus 로고    scopus 로고
    • Recapitulation of IVIG anti-inflammatory activity with a recombinant IgG Fc
    • COI: 1:CAS:528:DC%2BD1cXks1GhsLs%3D, PID: 18420934
    • Anthony RM, Nimmerjahn F, Ashline DJ, Reinhold VN, Paulson JC, Ravetch JV (2008a) Recapitulation of IVIG anti-inflammatory activity with a recombinant IgG Fc. Science 320:373–376
    • (2008) Science , vol.320 , pp. 373-376
    • Anthony, R.M.1    Nimmerjahn, F.2    Ashline, D.J.3    Reinhold, V.N.4    Paulson, J.C.5    Ravetch, J.V.6
  • 6
    • 58149378347 scopus 로고    scopus 로고
    • Identification of a receptor required for the anti-inflammatory activity of IVIG
    • COI: 1:CAS:528:DC%2BD1cXhsFCltr%2FI, PID: 19036920
    • Anthony RM, Wermeling F, Karlsson MC, Ravetch JV (2008b) Identification of a receptor required for the anti-inflammatory activity of IVIG. Proc Natl Acad Sci USA 105:19571–19578
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 19571-19578
    • Anthony, R.M.1    Wermeling, F.2    Karlsson, M.C.3    Ravetch, J.V.4
  • 7
    • 34247122497 scopus 로고    scopus 로고
    • The impact of glycosylation on the biological function and structure of human immunoglobulins
    • Arnold JN, Wormald MR, Sim RB, Rudd PM, Dwek RA (2006) The impact of glycosylation on the biological function and structure of human immunoglobulins. Annu Rev Immunol 25:21–50
    • (2006) Annu Rev Immunol , vol.25 , pp. 21-50
    • Arnold, J.N.1    Wormald, M.R.2    Sim, R.B.3    Rudd, P.M.4    Dwek, R.A.5
  • 8
    • 0020021127 scopus 로고
    • Carbohydrate-specific receptors of the liver
    • COI: 1:CAS:528:DyaL38Xks12ku78%3D, PID: 6287920
    • Ashwell G, Harford J (1982) Carbohydrate-specific receptors of the liver. Annu Rev Biochem 51:531–554
    • (1982) Annu Rev Biochem , vol.51 , pp. 531-554
    • Ashwell, G.1    Harford, J.2
  • 9
    • 70350055478 scopus 로고    scopus 로고
    • Branch-specific sialylation of IgG-Fc glycans by ST6Gal-I
    • COI: 1:CAS:528:DC%2BD1MXhtFOiu77F, PID: 19772356
    • Barb AW, Brady EK, Prestegard JH (2009) Branch-specific sialylation of IgG-Fc glycans by ST6Gal-I. Biochemistry 48:9705–9707
    • (2009) Biochemistry , vol.48 , pp. 9705-9707
    • Barb, A.W.1    Brady, E.K.2    Prestegard, J.H.3
  • 10
    • 84861883015 scopus 로고    scopus 로고
    • NMR characterization of immunoglobulin G Fc glycan motion on enzymatic sialylation
    • COI: 1:CAS:528:DC%2BC38XmvVGru78%3D, PID: 22574931
    • Barb AW, Meng L, Gao Z, Johnson RW, Moremen KW, Prestegard JH (2012) NMR characterization of immunoglobulin G Fc glycan motion on enzymatic sialylation. Biochemistry 51:4618–4626
    • (2012) Biochemistry , vol.51 , pp. 4618-4626
    • Barb, A.W.1    Meng, L.2    Gao, Z.3    Johnson, R.W.4    Moremen, K.W.5    Prestegard, J.H.6
  • 11
    • 84861804997 scopus 로고    scopus 로고
    • Selective deactivation of serum IgG: a general strategy for the enhancement of monoclonal antibody receptor interactions
    • COI: 1:CAS:528:DC%2BC38XmtlWhsb0%3D, PID: 22484364
    • Baruah K, Bowden TA, Krishna BA, Dwek RA, Crispin M, Scanlan CN (2012) Selective deactivation of serum IgG: a general strategy for the enhancement of monoclonal antibody receptor interactions. J Mol Biol 420:1–7
    • (2012) J Mol Biol , vol.420 , pp. 1-7
    • Baruah, K.1    Bowden, T.A.2    Krishna, B.A.3    Dwek, R.A.4    Crispin, M.5    Scanlan, C.N.6
  • 12
    • 33748355349 scopus 로고    scopus 로고
    • Reversal of immune thrombocytopenia in mice by cross-linking human immunoglobulin G with a high-affinity monoclonal antibody
    • COI: 1:CAS:528:DC%2BD28XhtFKjsbnJ, PID: 16925577
    • Bazin R, Lemieux R, Tremblay T (2006) Reversal of immune thrombocytopenia in mice by cross-linking human immunoglobulin G with a high-affinity monoclonal antibody. Br J Haematol 135:97–100
    • (2006) Br J Haematol , vol.135 , pp. 97-100
    • Bazin, R.1    Lemieux, R.2    Tremblay, T.3
  • 13
    • 78650351800 scopus 로고    scopus 로고
    • Ultra performance liquid chromatographic profiling of serum N-glycans for fast and efficient identification of cancer associated alterations in glycosylation
    • COI: 1:CAS:528:DC%2BC3cXhsVaisLjF, PID: 21073175
    • Bones J, Mittermayr S, O’Donoghue N, Guttman A, Rudd PM (2010) Ultra performance liquid chromatographic profiling of serum N-glycans for fast and efficient identification of cancer associated alterations in glycosylation. Anal Chem 82:10208–10215
    • (2010) Anal Chem , vol.82 , pp. 10208-10215
    • Bones, J.1    Mittermayr, S.2    O’Donoghue, N.3    Guttman, A.4    Rudd, P.M.5
  • 14
    • 84867836578 scopus 로고    scopus 로고
    • Revisiting the role of glycosylation in the structure of human IgG Fc
    • COI: 1:CAS:528:DC%2BC38XptlWiu7c%3D, PID: 22747430
    • Borrok MJ, Jung ST, Kang TH, Monzingo AF, Georgiou G (2012) Revisiting the role of glycosylation in the structure of human IgG Fc. ACS Chem Biol 7:1596–1602
    • (2012) ACS Chem Biol , vol.7 , pp. 1596-1602
    • Borrok, M.J.1    Jung, S.T.2    Kang, T.H.3    Monzingo, A.F.4    Georgiou, G.5
  • 15
    • 0037399064 scopus 로고    scopus 로고
    • Colony-stimulating factor-1-dependent macrophages are responsible for IVIG protection in antibody-induced autoimmune disease
    • COI: 1:CAS:528:DC%2BD3sXjtl2hurk%3D, PID: 12705859
    • Bruhns P, Samuelsson A, Pollard JW, Ravetch JV (2003) Colony-stimulating factor-1-dependent macrophages are responsible for IVIG protection in antibody-induced autoimmune disease. Immunity 18:573–581
    • (2003) Immunity , vol.18 , pp. 573-581
    • Bruhns, P.1    Samuelsson, A.2    Pollard, J.W.3    Ravetch, J.V.4
  • 16
    • 84901251341 scopus 로고    scopus 로고
    • Therapeutic effect of IVIG on inflammatory arthritis in mice is dependent on the Fc portion and independent of sialylation or basophils
    • COI: 1:CAS:528:DC%2BC2cXotFGisr0%3D, PID: 24760152
    • Campbell IK, Miescher S, Branch DR, Mott PJ, Lazarus AH, Han D, Maraskovsky E, Zuercher AW, Neschadim A, Leontyev D et al (2014) Therapeutic effect of IVIG on inflammatory arthritis in mice is dependent on the Fc portion and independent of sialylation or basophils. J Immunol 192:5031–5038
    • (2014) J Immunol , vol.192 , pp. 5031-5038
    • Campbell, I.K.1    Miescher, S.2    Branch, D.R.3    Mott, P.J.4    Lazarus, A.H.5    Han, D.6    Maraskovsky, E.7    Zuercher, A.W.8    Neschadim, A.9    Leontyev, D.10
  • 18
    • 41949141128 scopus 로고    scopus 로고
    • IgG glycan hydrolysis by a bacterial enzyme as a therapy against autoimmune conditions
    • PID: 18332429
    • Collin M, Shannon O, Bjorck L (2008) IgG glycan hydrolysis by a bacterial enzyme as a therapy against autoimmune conditions. Proc Natl Acad Sci USA 105:4265–4270
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 4265-4270
    • Collin, M.1    Shannon, O.2    Bjorck, L.3
  • 19
    • 84884309807 scopus 로고    scopus 로고
    • Crystal structure of sialylated IgG Fc: implications for the mechanism of intravenous immunoglobulin therapy
    • COI: 1:CAS:528:DC%2BC3sXhsFOhtr3M, PID: 23929778
    • Crispin M, Yu X, Bowden TA (2013) Crystal structure of sialylated IgG Fc: implications for the mechanism of intravenous immunoglobulin therapy. Proc Natl Acad Sci USA 110:E3544–3546
    • (2013) Proc Natl Acad Sci USA , vol.110 , pp. E3544-E3546
    • Crispin, M.1    Yu, X.2    Bowden, T.A.3
  • 20
    • 84902684505 scopus 로고    scopus 로고
    • Crystal structure of deglycosylated human IgG4-Fc
    • COI: 1:CAS:528:DC%2BC2cXhsVeiu7fI, PID: 24956411
    • Davies AM, Jefferis R, Sutton BJ (2014a) Crystal structure of deglycosylated human IgG4-Fc. Mol Immunol 62:46–53
    • (2014) Mol Immunol , vol.62 , pp. 46-53
    • Davies, A.M.1    Jefferis, R.2    Sutton, B.J.3
  • 23
    • 0019522383 scopus 로고
    • Crystallographic refinement and atomic models of a human Fc fragment and its complex with fragment B of protein A from Staphylococcus aureus at 2.9- and 2.8-A resolution
    • COI: 1:CAS:528:DyaL3MXitVKqtrc%3D, PID: 7236608
    • Deisenhofer J (1981) Crystallographic refinement and atomic models of a human Fc fragment and its complex with fragment B of protein A from Staphylococcus aureus at 2.9- and 2.8-A resolution. Biochemistry 20:2361–2370
    • (1981) Biochemistry , vol.20 , pp. 2361-2370
    • Deisenhofer, J.1
  • 25
    • 84864124216 scopus 로고    scopus 로고
    • High-throughput quantitative N-glycan analysis of glycoproteins
    • COI: 1:CAS:528:DC%2BC3sXitFagsrk%3D, PID: 22735961
    • Doherty M, McManus CA, Duke R, Rudd PM (2012) High-throughput quantitative N-glycan analysis of glycoproteins. Methods Mol Biol 899:293–313
    • (2012) Methods Mol Biol , vol.899 , pp. 293-313
    • Doherty, M.1    McManus, C.A.2    Duke, R.3    Rudd, P.M.4
  • 26
    • 0032247499 scopus 로고    scopus 로고
    • Biological importance of glycosylation
    • COI: 1:CAS:528:DyaK1MXktV2rur8%3D, PID: 9890515
    • Dwek RA (1998) Biological importance of glycosylation. Dev Biol Stand 96:43–47
    • (1998) Dev Biol Stand , vol.96 , pp. 43-47
    • Dwek, R.A.1
  • 27
    • 84859486843 scopus 로고    scopus 로고
    • Remarkable transglycosylation activity of glycosynthase mutants of endo-D, an endo-beta-N-acetylglucosaminidase from Streptococcus pneumoniae
    • COI: 1:CAS:528:DC%2BC38XkvVWltrs%3D, PID: 22318728
    • Fan SQ, Huang W, Wang LX (2012) Remarkable transglycosylation activity of glycosynthase mutants of endo-D, an endo-beta-N-acetylglucosaminidase from Streptococcus pneumoniae. J Biol Chem 287:11272–11281
    • (2012) J Biol Chem , vol.287 , pp. 11272-11281
    • Fan, S.Q.1    Huang, W.2    Wang, L.X.3
  • 29
    • 79961233787 scopus 로고    scopus 로고
    • Unique carbohydrate–carbohydrate interactions are required for high affinity binding between FcgammaRIII and antibodies lacking core fucose
    • COI: 1:CAS:528:DC%2BC3MXhtVenu7jF, PID: 21768335
    • Ferrara C, Grau S, Jager C, Sondermann P, Brunker P, Waldhauer I, Hennig M, Ruf A, Rufer AC, Stihle M et al (2011) Unique carbohydrate–carbohydrate interactions are required for high affinity binding between FcgammaRIII and antibodies lacking core fucose. Proc Natl Acad Sci USA 108:12669–12674
    • (2011) Proc Natl Acad Sci USA , vol.108 , pp. 12669-12674
    • Ferrara, C.1    Grau, S.2    Jager, C.3    Sondermann, P.4    Brunker, P.5    Waldhauer, I.6    Hennig, M.7    Ruf, A.8    Rufer, A.C.9    Stihle, M.10
  • 30
    • 33646172632 scopus 로고    scopus 로고
    • The carbohydrate at FcgammaRIIIa Asn-162. An element required for high affinity binding to non-fucosylated IgG glycoforms
    • COI: 1:CAS:528:DC%2BD28Xhs1ektrs%3D, PID: 16330541
    • Ferrara C, Stuart F, Sondermann P, Brunker P, Umana P (2006) The carbohydrate at FcgammaRIIIa Asn-162. An element required for high affinity binding to non-fucosylated IgG glycoforms. J Biol Chem 281:5032–5036
    • (2006) J Biol Chem , vol.281 , pp. 5032-5036
    • Ferrara, C.1    Stuart, F.2    Sondermann, P.3    Brunker, P.4    Umana, P.5
  • 31
    • 7044274809 scopus 로고    scopus 로고
    • Molecular cloning of Mucor hiemalis endo-beta-N-acetylglucosaminidase and some properties of the recombinant enzyme
    • COI: 1:CAS:528:DC%2BD2cXpt1Sqsbc%3D, PID: 15519295
    • Fujita K, Kobayashi K, Iwamatsu A, Takeuchi M, Kumagai H, Yamamoto K (2004) Molecular cloning of Mucor hiemalis endo-beta-N-acetylglucosaminidase and some properties of the recombinant enzyme. Arch Biochem Biophys 432:41–49
    • (2004) Arch Biochem Biophys , vol.432 , pp. 41-49
    • Fujita, K.1    Kobayashi, K.2    Iwamatsu, A.3    Takeuchi, M.4    Kumagai, H.5    Yamamoto, K.6
  • 32
    • 2142813035 scopus 로고    scopus 로고
    • V region carbohydrate and antibody expression
    • COI: 1:CAS:528:DC%2BD2cXjt1Ckt7s%3D, PID: 15100290
    • Gala FA, Morrison SL (2004) V region carbohydrate and antibody expression. J Immunol 172:5489–5494
    • (2004) J Immunol , vol.172 , pp. 5489-5494
    • Gala, F.A.1    Morrison, S.L.2
  • 33
    • 0027367160 scopus 로고
    • One percent of human circulating B lymphocytes are capable of producing the natural anti-Gal antibody
    • COI: 1:CAS:528:DyaK3sXms1ymtb4%3D, PID: 7691263
    • Galili U, Anaraki F, Thall A, Hill-Black C, Radic M (1993) One percent of human circulating B lymphocytes are capable of producing the natural anti-Gal antibody. Blood 82:2485–2493
    • (1993) Blood , vol.82 , pp. 2485-2493
    • Galili, U.1    Anaraki, F.2    Thall, A.3    Hill-Black, C.4    Radic, M.5
  • 34
    • 0028877254 scopus 로고
    • Stoichiometry and thermodynamics of the interaction between the Fc fragment of human IgG1 and its low-affinity receptor Fc gamma RIII
    • COI: 1:CAS:528:DyaK2MXovFWmurk%3D, PID: 7577916
    • Ghirlando R, Keown MB, Mackay GA, Lewis MS, Unkeless JC, Gould HJ (1995) Stoichiometry and thermodynamics of the interaction between the Fc fragment of human IgG1 and its low-affinity receptor Fc gamma RIII. Biochemistry 34:13320–13327
    • (1995) Biochemistry , vol.34 , pp. 13320-13327
    • Ghirlando, R.1    Keown, M.B.2    Mackay, G.A.3    Lewis, M.S.4    Unkeless, J.C.5    Gould, H.J.6
  • 35
    • 84957369935 scopus 로고    scopus 로고
    • Chemoenzymatic Glyco-engineering of Monoclonal Antibodies
    • PID: 26082235
    • Giddens JP, Wang LX (2015) Chemoenzymatic Glyco-engineering of Monoclonal Antibodies. Methods Mol Biol 1321:375–387
    • (2015) Methods Mol Biol , vol.1321 , pp. 375-387
    • Giddens, J.P.1    Wang, L.X.2
  • 36
    • 79958837668 scopus 로고    scopus 로고
    • High-mannose glycans on the Fc region of therapeutic IgG antibodies increase serum clearance in humans
    • COI: 1:CAS:528:DC%2BC3MXnsFWlur8%3D, PID: 21421994
    • Goetze AM, Liu YD, Zhang Z, Shah B, Lee E, Bondarenko PV, Flynn GC (2011) High-mannose glycans on the Fc region of therapeutic IgG antibodies increase serum clearance in humans. Glycobiology 21:949–959
    • (2011) Glycobiology , vol.21 , pp. 949-959
    • Goetze, A.M.1    Liu, Y.D.2    Zhang, Z.3    Shah, B.4    Lee, E.5    Bondarenko, P.V.6    Flynn, G.C.7
  • 37
    • 0020286659 scopus 로고
    • Structure of the glycopeptides of a human gamma 1-immunoglobulin G (Tem) myeloma protein as determined by 360-megahertz nuclear magnetic resonance spectroscopy
    • COI: 1:CAS:528:DyaL3sXjt1OhsQ%3D%3D, PID: 7165834
    • Grey AA, Narasimhan S, Brisson JR, Schachter H, Carver JP (1982) Structure of the glycopeptides of a human gamma 1-immunoglobulin G (Tem) myeloma protein as determined by 360-megahertz nuclear magnetic resonance spectroscopy. Can J Biochem 60:1123–1131
    • (1982) Can J Biochem , vol.60 , pp. 1123-1131
    • Grey, A.A.1    Narasimhan, S.2    Brisson, J.R.3    Schachter, H.4    Carver, J.P.5
  • 38
    • 79959555556 scopus 로고    scopus 로고
    • Enrichment of sialylated IgG by lectin fractionation does not enhance the efficacy of immunoglobulin G in a murine model of immune thrombocytopenia
    • COI: 1:CAS:528:DC%2BC3MXotF2ms7k%3D, PID: 21731683
    • Guhr T, Bloem J, Derksen NI, Wuhrer M, Koenderman AH, Aalberse RC, Rispens T (2011) Enrichment of sialylated IgG by lectin fractionation does not enhance the efficacy of immunoglobulin G in a murine model of immune thrombocytopenia. PloS One 6:e21246
    • (2011) PloS One , vol.6
    • Guhr, T.1    Bloem, J.2    Derksen, N.I.3    Wuhrer, M.4    Koenderman, A.H.5    Aalberse, R.C.6    Rispens, T.7
  • 39
    • 80052598704 scopus 로고    scopus 로고
    • Biochemical and biophysical characterization of humanized IgG1 produced in Pichia pastoris
    • PID: 22048694
    • Ha S, Wang Y, Rustandi RR (2011) Biochemical and biophysical characterization of humanized IgG1 produced in Pichia pastoris. MAbs 3:453–460
    • (2011) MAbs , vol.3 , pp. 453-460
    • Ha, S.1    Wang, Y.2    Rustandi, R.R.3
  • 40
    • 84957991319 scopus 로고    scopus 로고
    • N-glycosylation heterogeneity and the influence on structure, function and pharmacokinetics of monoclonal antibodies and Fc fusion proteins
    • COI: 1:CAS:528:DC%2BC28Xps1SktA%3D%3D, PID: 26775146
    • Higel F, Seidl A, Sorgel F, Friess W (2016) N-glycosylation heterogeneity and the influence on structure, function and pharmacokinetics of monoclonal antibodies and Fc fusion proteins. Eur J Pharm Biopharm 100:94–100
    • (2016) Eur J Pharm Biopharm , vol.100 , pp. 94-100
    • Higel, F.1    Seidl, A.2    Sorgel, F.3    Friess, W.4
  • 41
    • 33646093725 scopus 로고    scopus 로고
    • Differential glycosylation of polyclonal IgG, IgG-Fc and IgG-Fab isolated from the sera of patients with ANCA-associated systemic vasculitis
    • COI: 1:CAS:528:DC%2BD28Xjsl2mtrs%3D, PID: 16413679
    • Holland M, Yagi H, Takahashi N, Kato K, Savage CO, Goodall DM, Jefferis R (2006) Differential glycosylation of polyclonal IgG, IgG-Fc and IgG-Fab isolated from the sera of patients with ANCA-associated systemic vasculitis. Biochim Biophys Acta 1760:669–677
    • (2006) Biochim Biophys Acta , vol.1760 , pp. 669-677
    • Holland, M.1    Yagi, H.2    Takahashi, N.3    Kato, K.4    Savage, C.O.5    Goodall, D.M.6    Jefferis, R.7
  • 42
    • 84864238717 scopus 로고    scopus 로고
    • Chemoenzymatic glycoengineering of intact IgG antibodies for gain of functions
    • COI: 1:CAS:528:DC%2BC38XpsV2gsb8%3D, PID: 22747414
    • Huang W, Giddens J, Fan SQ, Toonstra C, Wang LX (2012) Chemoenzymatic glycoengineering of intact IgG antibodies for gain of functions. J Am Chem Soc 134:12308–12318
    • (2012) J Am Chem Soc , vol.134 , pp. 12308-12318
    • Huang, W.1    Giddens, J.2    Fan, S.Q.3    Toonstra, C.4    Wang, L.X.5
  • 43
    • 33646740982 scopus 로고    scopus 로고
    • Nonfucosylated therapeutic IgG1 antibody can evade the inhibitory effect of serum immunoglobulin G on antibody-dependent cellular cytotoxicity through its high binding to FcgammaRIIIa
    • COI: 1:CAS:528:DC%2BD28XltlamtLY%3D, PID: 16675584
    • Iida S, Misaka H, Inoue M, Shibata M, Nakano R, Yamane-Ohnuki N, Wakitani M, Yano K, Shitara K, Satoh M (2006) Nonfucosylated therapeutic IgG1 antibody can evade the inhibitory effect of serum immunoglobulin G on antibody-dependent cellular cytotoxicity through its high binding to FcgammaRIIIa. Clin Cancer Res 12:2879–2887
    • (2006) Clin Cancer Res , vol.12 , pp. 2879-2887
    • Iida, S.1    Misaka, H.2    Inoue, M.3    Shibata, M.4    Nakano, R.5    Yamane-Ohnuki, N.6    Wakitani, M.7    Yano, K.8    Shitara, K.9    Satoh, M.10
  • 44
    • 84863393084 scopus 로고    scopus 로고
    • Defucosylated anti-CCR4 monoclonal antibody (KW-0761) for relapsed adult T-cell leukemia-lymphoma: a multicenter phase II study
    • COI: 1:CAS:528:DC%2BC38XntV2lsbo%3D, PID: 22312108
    • Ishida T, Joh T, Uike N, Yamamoto K, Utsunomiya A, Yoshida S, Saburi Y, Miyamoto T, Takemoto S, Suzushima H et al (2012) Defucosylated anti-CCR4 monoclonal antibody (KW-0761) for relapsed adult T-cell leukemia-lymphoma: a multicenter phase II study. J Clin Oncol 30:837–842
    • (2012) J Clin Oncol , vol.30 , pp. 837-842
    • Ishida, T.1    Joh, T.2    Uike, N.3    Yamamoto, K.4    Utsunomiya, A.5    Yoshida, S.6    Saburi, Y.7    Miyamoto, T.8    Takemoto, S.9    Suzushima, H.10
  • 45
    • 84991522888 scopus 로고    scopus 로고
    • A novel approach to predict cetuximab-induced hypersensitivity reaction: detection of drug-specific IgE on basophils
    • COI: 1:CAS:528:DC%2BC28XhtVKisLzJ, PID: 26880699
    • Iwamoto T, Okamoto A, Ishinaga H, Shimizu K, Gayle AA, Arai N, Takeuchi K, Okuda M (2016) A novel approach to predict cetuximab-induced hypersensitivity reaction: detection of drug-specific IgE on basophils. Cancer Med 5:1004–1012
    • (2016) Cancer Med , vol.5 , pp. 1004-1012
    • Iwamoto, T.1    Okamoto, A.2    Ishinaga, H.3    Shimizu, K.4    Gayle, A.A.5    Arai, N.6    Takeuchi, K.7    Okuda, M.8
  • 46
    • 61649087668 scopus 로고    scopus 로고
    • Glycosylation as a strategy to improve antibody-based therapeutics
    • COI: 1:CAS:528:DC%2BD1MXisVShtb0%3D, PID: 19247305
    • Jefferis R (2009) Glycosylation as a strategy to improve antibody-based therapeutics. Nat Rev Drug Discov 8:226–234
    • (2009) Nat Rev Drug Discov , vol.8 , pp. 226-234
    • Jefferis, R.1
  • 47
    • 84865677743 scopus 로고    scopus 로고
    • Isotype and glycoform selection for antibody therapeutics
    • COI: 1:CAS:528:DC%2BC38Xlt1ymtL0%3D, PID: 22465822
    • Jefferis R (2012) Isotype and glycoform selection for antibody therapeutics. Arch Biochem Biophys 526:159–166
    • (2012) Arch Biochem Biophys , vol.526 , pp. 159-166
    • Jefferis, R.1
  • 48
    • 85020162296 scopus 로고    scopus 로고
    • Characterization of biosimilar biologics: the link between structure and functions
    • Endrenyi L, Declerck P, Chow S-C, (eds), CRC Press, Boca Raton
    • Jefferis R (2017) Characterization of biosimilar biologics: the link between structure and functions. In: Endrenyi L, Declerck P, Chow S-C (eds) Drugs and the pharmaceutical sciences. CRC Press, Boca Raton, pp 109–149
    • (2017) Drugs and the pharmaceutical sciences , pp. 109-149
    • Jefferis, R.1
  • 49
    • 84904344421 scopus 로고    scopus 로고
    • Aglycosylated full-length IgG antibodies: steps toward next-generation immunotherapeutics
    • COI: 1:CAS:528:DC%2BC2cXhtlCisbbN, PID: 25035939
    • Ju MS, Jung ST (2014) Aglycosylated full-length IgG antibodies: steps toward next-generation immunotherapeutics. Curr Opin Biotechnol 30:128–139
    • (2014) Curr Opin Biotechnol , vol.30 , pp. 128-139
    • Ju, M.S.1    Jung, S.T.2
  • 50
    • 84940959004 scopus 로고    scopus 로고
    • Structural consequences of aglycosylated IgG Fc variants evolved for FcgammaRI binding
    • COI: 1:CAS:528:DC%2BC2MXhtVyht7vK, PID: 26153451
    • Ju MS, Na JH, Yu YG, Kim JY, Jeong C, Jung ST (2015) Structural consequences of aglycosylated IgG Fc variants evolved for FcgammaRI binding. Mol Immunol 67:350–356
    • (2015) Mol Immunol , vol.67 , pp. 350-356
    • Ju, M.S.1    Na, J.H.2    Yu, Y.G.3    Kim, J.Y.4    Jeong, C.5    Jung, S.T.6
  • 51
    • 80052622662 scopus 로고    scopus 로고
    • Bypassing glycosylation: engineering aglycosylated full-length IgG antibodies for human therapy
    • COI: 1:CAS:528:DC%2BC3MXhsFOhtLfJ, PID: 21420850
    • Jung ST, Kang TH, Kelton W, Georgiou G (2011) Bypassing glycosylation: engineering aglycosylated full-length IgG antibodies for human therapy. Curr Opin Biotechnol 22:858–867
    • (2011) Curr Opin Biotechnol , vol.22 , pp. 858-867
    • Jung, S.T.1    Kang, T.H.2    Kelton, W.3    Georgiou, G.4
  • 52
    • 76249100176 scopus 로고    scopus 로고
    • Aglycosylated IgG variants expressed in bacteria that selectively bind FcgammaRI potentiate tumor cell killing by monocyte-dendritic cells
    • COI: 1:CAS:528:DC%2BC3cXhtFCmsr4%3D, PID: 20080725
    • Jung ST, Reddy ST, Kang TH, Borrok MJ, Sandlie I, Tucker PW, Georgiou G (2010) Aglycosylated IgG variants expressed in bacteria that selectively bind FcgammaRI potentiate tumor cell killing by monocyte-dendritic cells. Proc Natl Acad Sci USA 107:604–609
    • (2010) Proc Natl Acad Sci USA , vol.107 , pp. 604-609
    • Jung, S.T.1    Reddy, S.T.2    Kang, T.H.3    Borrok, M.J.4    Sandlie, I.5    Tucker, P.W.6    Georgiou, G.7
  • 53
    • 33845590523 scopus 로고    scopus 로고
    • Comparison of biological activity among nonfucosylated therapeutic IgG1 antibodies with three different N-linked Fc oligosaccharides: the high-mannose, hybrid, and complex types
    • COI: 1:CAS:528:DC%2BD28XhtlChtbrK, PID: 17012310
    • Kanda Y, Yamada T, Mori K, Okazaki A, Inoue M, Kitajima-Miyama K, Kuni-Kamochi R, Nakano R, Yano K, Kakita S et al (2007) Comparison of biological activity among nonfucosylated therapeutic IgG1 antibodies with three different N-linked Fc oligosaccharides: the high-mannose, hybrid, and complex types. Glycobiology 17:104–118
    • (2007) Glycobiology , vol.17 , pp. 104-118
    • Kanda, Y.1    Yamada, T.2    Mori, K.3    Okazaki, A.4    Inoue, M.5    Kitajima-Miyama, K.6    Kuni-Kamochi, R.7    Nakano, R.8    Yano, K.9    Kakita, S.10
  • 54
    • 33746888249 scopus 로고    scopus 로고
    • Anti-inflammatory activity of immunoglobulin G resulting from Fc sialylation
    • COI: 1:CAS:528:DC%2BD28Xnsl2hsbY%3D, PID: 16888140
    • Kaneko Y, Nimmerjahn F, Ravetch JV (2006) Anti-inflammatory activity of immunoglobulin G resulting from Fc sialylation. Science 313:670–673
    • (2006) Science , vol.313 , pp. 670-673
    • Kaneko, Y.1    Nimmerjahn, F.2    Ravetch, J.V.3
  • 55
    • 84951291802 scopus 로고    scopus 로고
    • A monosaccharide residue is sufficient to maintain mouse and human IgG subclass activity and directs IgG effector functions to cellular Fc receptors
    • COI: 1:CAS:528:DC%2BC2MXhvFKkt7jP, PID: 26670049
    • Kao D, Danzer H, Collin M, Gross A, Eichler J, Stambuk J, Lauc G, Lux A, Nimmerjahn F (2015) A monosaccharide residue is sufficient to maintain mouse and human IgG subclass activity and directs IgG effector functions to cellular Fc receptors. Cell Rep 13:2376–2385
    • (2015) Cell Rep , vol.13 , pp. 2376-2385
    • Kao, D.1    Danzer, H.2    Collin, M.3    Gross, A.4    Eichler, J.5    Stambuk, J.6    Lauc, G.7    Lux, A.8    Nimmerjahn, F.9
  • 56
    • 0036798689 scopus 로고    scopus 로고
    • Identification of an endo-beta-N-acetylglucosaminidase gene in Caenorhabditis elegans and its expression in Escherichia coli
    • COI: 1:CAS:528:DC%2BD38XoslGqtb0%3D, PID: 12244070
    • Kato T, Fujita K, Takeuchi M, Kobayashi K, Natsuka S, Ikura K, Kumagai H, Yamamoto K (2002) Identification of an endo-beta-N-acetylglucosaminidase gene in Caenorhabditis elegans and its expression in Escherichia coli. Glycobiology 12:581–587
    • (2002) Glycobiology , vol.12 , pp. 581-587
    • Kato, T.1    Fujita, K.2    Takeuchi, M.3    Kobayashi, K.4    Natsuka, S.5    Ikura, K.6    Kumagai, H.7    Yamamoto, K.8
  • 57
    • 0030452755 scopus 로고    scopus 로고
    • Enzymatic synthesis of chondroitin and its derivatives catalyzed by hyaluronidase
    • COI: 1:CAS:528:DyaK28XnsVCgsr8%3D
    • Kobayashi S, Kiyosada T, Shoda S-I (1996) Enzymatic synthesis of chondroitin and its derivatives catalyzed by hyaluronidase. J Am Chem Soc 118:13113–13114
    • (1996) J Am Chem Soc , vol.118 , pp. 13113-13114
    • Kobayashi, S.1    Kiyosada, T.2    Shoda, S.-I.3
  • 58
    • 0030611643 scopus 로고    scopus 로고
    • Fc gammaRIIIa-158V/F polymorphism influences the binding of IgG by natural killer cell Fc gammaRIIIa, independently of the Fc gammaRIIIa-48L/R/H phenotype
    • COI: 1:CAS:528:DyaK2sXkvVWgt74%3D, PID: 9242542
    • Koene HR, Kleijer M, Algra J, Roos D, von dem Borne AE, de Haas M (1997) Fc gammaRIIIa-158V/F polymorphism influences the binding of IgG by natural killer cell Fc gammaRIIIa, independently of the Fc gammaRIIIa-48L/R/H phenotype. Blood 90:1109–1114
    • (1997) Blood , vol.90 , pp. 1109-1114
    • Koene, H.R.1    Kleijer, M.2    Algra, J.3    Roos, D.4    von dem Borne, A.E.5    de Haas, M.6
  • 59
    • 0037474543 scopus 로고    scopus 로고
    • Structural analysis of human IgG-Fc glycoforms reveals a correlation between glycosylation and structural integrity
    • COI: 1:CAS:528:DC%2BD3sXjtFGjuw%3D%3D, PID: 12527303
    • Krapp S, Mimura Y, Jefferis R, Huber R, Sondermann P (2003) Structural analysis of human IgG-Fc glycoforms reveals a correlation between glycosylation and structural integrity. J Mol Biol 325:979–989
    • (2003) J Mol Biol , vol.325 , pp. 979-989
    • Krapp, S.1    Mimura, Y.2    Jefferis, R.3    Huber, R.4    Sondermann, P.5
  • 60
    • 84941309144 scopus 로고    scopus 로고
    • Glycoengineered monoclonal antibodies with homogeneous glycan (M3, G0, G2, and A2) using a chemoenzymatic approach have different affinities for FcgammaRIIIa and Variable antibody-dependent cellular cytotoxicity activities
    • PID: 26200113
    • Kurogochi M, Mori M, Osumi K, Tojino M, Sugawara S, Takashima S, Hirose Y, Tsukimura W, Mizuno M, Amano J et al (2015) Glycoengineered monoclonal antibodies with homogeneous glycan (M3, G0, G2, and A2) using a chemoenzymatic approach have different affinities for FcgammaRIIIa and Variable antibody-dependent cellular cytotoxicity activities. PloS One 10:e0132848
    • (2015) PloS One , vol.10
    • Kurogochi, M.1    Mori, M.2    Osumi, K.3    Tojino, M.4    Sugawara, S.5    Takashima, S.6    Hirose, Y.7    Tsukimura, W.8    Mizuno, M.9    Amano, J.10
  • 62
    • 84861858882 scopus 로고    scopus 로고
    • Mouse background and IVIG dosage are critical in establishing the role of inhibitory Fcgamma receptor for the amelioration of experimental ITP
    • COI: 1:CAS:528:DC%2BC38XhtVWjs7rK, PID: 22508937
    • Leontyev D, Katsman Y, Branch DR (2012a) Mouse background and IVIG dosage are critical in establishing the role of inhibitory Fcgamma receptor for the amelioration of experimental ITP. Blood 119:5261–5264
    • (2012) Blood , vol.119 , pp. 5261-5264
    • Leontyev, D.1    Katsman, Y.2    Branch, D.R.3
  • 63
    • 84865030107 scopus 로고    scopus 로고
    • Sialylation-independent mechanism involved in the amelioration of murine immune thrombocytopenia using intravenous gammaglobulin
    • COI: 1:CAS:528:DC%2BC38XhsVCqs7rF, PID: 22257295
    • Leontyev D, Katsman Y, Ma XZ, Miescher S, Kasermann F, Branch DR (2012b) Sialylation-independent mechanism involved in the amelioration of murine immune thrombocytopenia using intravenous gammaglobulin. Transfusion 52:1799–1805
    • (2012) Transfusion , vol.52 , pp. 1799-1805
    • Leontyev, D.1    Katsman, Y.2    Ma, X.Z.3    Miescher, S.4    Kasermann, F.5    Branch, D.R.6
  • 64
    • 22144450662 scopus 로고    scopus 로고
    • Highly efficient endoglycosidase-catalyzed synthesis of glycopeptides using oligosaccharide oxazolines as donor substrates
    • COI: 1:CAS:528:DC%2BD2MXltVylsrw%3D, PID: 15998066
    • Li B, Zeng Y, Hauser S, Song H, Wang LX (2005) Highly efficient endoglycosidase-catalyzed synthesis of glycopeptides using oligosaccharide oxazolines as donor substrates. J Am Chem Soc 127:9692–9693
    • (2005) J Am Chem Soc , vol.127 , pp. 9692-9693
    • Li, B.1    Zeng, Y.2    Hauser, S.3    Song, H.4    Wang, L.X.5
  • 66
    • 84982803694 scopus 로고    scopus 로고
    • Glycosynthase mutants of endoglycosidase S2 show potent transglycosylation activity and remarkably relaxed substrate specificity for antibody glycosylation remodeling
    • COI: 1:CAS:528:DC%2BC28Xht1yqt77M, PID: 27288408
    • Li T, Tong X, Yang Q, Giddens JP, Wang LX (2016) Glycosynthase mutants of endoglycosidase S2 show potent transglycosylation activity and remarkably relaxed substrate specificity for antibody glycosylation remodeling. J Biol Chem 291:16508–16518
    • (2016) J Biol Chem , vol.291 , pp. 16508-16518
    • Li, T.1    Tong, X.2    Yang, Q.3    Giddens, J.P.4    Wang, L.X.5
  • 68
    • 84929154056 scopus 로고    scopus 로고
    • Antibody glycosylation and its impact on the pharmacokinetics and pharmacodynamics of monoclonal antibodies and Fc-fusion proteins
    • COI: 1:CAS:528:DC%2BC2MXmsFSnsbs%3D, PID: 25872915
    • Liu L (2015) Antibody glycosylation and its impact on the pharmacokinetics and pharmacodynamics of monoclonal antibodies and Fc-fusion proteins. J Pharm Sci 104:1866–1884
    • (2015) J Pharm Sci , vol.104 , pp. 1866-1884
    • Liu, L.1
  • 69
    • 85017619523 scopus 로고    scopus 로고
    • Pharmacokinetics of monoclonal antibodies and Fc-fusion proteins
    • Liu L (2017) Pharmacokinetics of monoclonal antibodies and Fc-fusion proteins. Protein Cell. doi:10.1007/s13238-017-0408-4
    • (2017) Protein Cell
    • Liu, L.1
  • 70
    • 79961208871 scopus 로고    scopus 로고
    • Pharmacokinetics of IgG1 monoclonal antibodies produced in humanized Pichia pastoris with specific glycoforms: a comparative study with CHO produced materials
    • COI: 1:CAS:528:DC%2BC3MXhtVaisbfM, PID: 21723741
    • Liu L, Stadheim A, Hamuro L, Pittman T, Wang W, Zha D, Hochman J, Prueksaritanont T (2011) Pharmacokinetics of IgG1 monoclonal antibodies produced in humanized Pichia pastoris with specific glycoforms: a comparative study with CHO produced materials. Biologicals 39:205–210
    • (2011) Biologicals , vol.39 , pp. 205-210
    • Liu, L.1    Stadheim, A.2    Hamuro, L.3    Pittman, T.4    Wang, W.5    Zha, D.6    Hochman, J.7    Prueksaritanont, T.8
  • 71
    • 0025086946 scopus 로고
    • A protein structural change in aglycosylated IgG3 correlates with loss of huFc gamma R1 and huFc gamma R111 binding and/or activation
    • COI: 1:CAS:528:DyaK3MXpvFGrtw%3D%3D, PID: 2174119
    • Lund J, Tanaka T, Takahashi N, Sarmay G, Arata Y, Jefferis R (1990) A protein structural change in aglycosylated IgG3 correlates with loss of huFc gamma R1 and huFc gamma R111 binding and/or activation. Mol Immunol 27:1145–1153
    • (1990) Mol Immunol , vol.27 , pp. 1145-1153
    • Lund, J.1    Tanaka, T.2    Takahashi, N.3    Sarmay, G.4    Arata, Y.5    Jefferis, R.6
  • 72
    • 0035977068 scopus 로고    scopus 로고
    • The human low affinity Fcgamma receptors IIa, IIb, and III bind IgG with fast kinetics and distinct thermodynamic properties
    • COI: 1:CAS:528:DC%2BD3MXovFegurc%3D, PID: 11544262
    • Maenaka K, van der Merwe PA, Stuart DI, Jones EY, Sondermann P (2001) The human low affinity Fcgamma receptors IIa, IIb, and III bind IgG with fast kinetics and distinct thermodynamic properties. J Biol Chem 276:44898–44904
    • (2001) J Biol Chem , vol.276 , pp. 44898-44904
    • Maenaka, K.1    van der Merwe, P.A.2    Stuart, D.I.3    Jones, E.Y.4    Sondermann, P.5
  • 74
    • 34047142084 scopus 로고    scopus 로고
    • Structural comparison of fucosylated and nonfucosylated Fc fragments of human immunoglobulin G1
    • COI: 1:CAS:528:DC%2BD2sXjvFemsL0%3D, PID: 17368483
    • Matsumiya S, Yamaguchi Y, Saito J, Nagano M, Sasakawa H, Otaki S, Satoh M, Shitara K, Kato K (2007) Structural comparison of fucosylated and nonfucosylated Fc fragments of human immunoglobulin G1. J Mol Biol 368:767–779
    • (2007) J Mol Biol , vol.368 , pp. 767-779
    • Matsumiya, S.1    Yamaguchi, Y.2    Saito, J.3    Nagano, M.4    Sasakawa, H.5    Otaki, S.6    Satoh, M.7    Shitara, K.8    Kato, K.9
  • 75
    • 34548409568 scopus 로고    scopus 로고
    • Contrasting glycosylation profiles between Fab and Fc of a human IgG protein studied by electrospray ionization mass spectrometry
    • COI: 1:CAS:528:DC%2BD2sXhtVWmtrzI, PID: 17714731
    • Mimura Y, Ashton PR, Takahashi N, Harvey DJ, Jefferis R (2007) Contrasting glycosylation profiles between Fab and Fc of a human IgG protein studied by electrospray ionization mass spectrometry. J Immunol Methods 326:116–126
    • (2007) J Immunol Methods , vol.326 , pp. 116-126
    • Mimura, Y.1    Ashton, P.R.2    Takahashi, N.3    Harvey, D.J.4    Jefferis, R.5
  • 76
    • 0035081693 scopus 로고    scopus 로고
    • The influence of glycosylation on the thermal stability and effector function expression of human IgG1-Fc: properties of a series of truncated glycoforms
    • COI: 1:CAS:528:DC%2BD3MXitFyrsbg%3D, PID: 11275255
    • Mimura Y, Church S, Ghirlando R, Ashton PR, Dong S, Goodall M, Lund J, Jefferis R (2000) The influence of glycosylation on the thermal stability and effector function expression of human IgG1-Fc: properties of a series of truncated glycoforms. Mol Immunol 37:697–706
    • (2000) Mol Immunol , vol.37 , pp. 697-706
    • Mimura, Y.1    Church, S.2    Ghirlando, R.3    Ashton, P.R.4    Dong, S.5    Goodall, M.6    Lund, J.7    Jefferis, R.8
  • 79
  • 80
    • 80054944116 scopus 로고    scopus 로고
    • Structural basis for improved efficacy of therapeutic antibodies on defucosylation of their Fc glycans
    • COI: 1:CAS:528:DC%2BC3MXhsFSjsrzO, PID: 22023369
    • Mizushima T, Yagi H, Takemoto E, Shibata-Koyama M, Isoda Y, Iida S, Masuda K, Satoh M, Kato K (2011) Structural basis for improved efficacy of therapeutic antibodies on defucosylation of their Fc glycans. Genes Cells 16:1071–1080
    • (2011) Genes Cells , vol.16 , pp. 1071-1080
    • Mizushima, T.1    Yagi, H.2    Takemoto, E.3    Shibata-Koyama, M.4    Isoda, Y.5    Iida, S.6    Masuda, K.7    Satoh, M.8    Kato, K.9
  • 81
    • 77951561987 scopus 로고    scopus 로고
    • Increasing the efficacy of CD20 antibody therapy through the engineering of a new type II anti-CD20 antibody with enhanced direct and immune effector cell-mediated B-cell cytotoxicity
    • COI: 1:CAS:528:DC%2BC3cXnsFKnt7w%3D, PID: 20194898
    • Mossner E, Brunker P, Moser S, Puntener U, Schmidt C, Herter S, Grau R, Gerdes C, Nopora A, van Puijenbroek E et al (2010) Increasing the efficacy of CD20 antibody therapy through the engineering of a new type II anti-CD20 antibody with enhanced direct and immune effector cell-mediated B-cell cytotoxicity. Blood 115:4393–4402
    • (2010) Blood , vol.115 , pp. 4393-4402
    • Mossner, E.1    Brunker, P.2    Moser, S.3    Puntener, U.4    Schmidt, C.5    Herter, S.6    Grau, R.7    Gerdes, C.8    Nopora, A.9    van Puijenbroek, E.10
  • 82
    • 0034950461 scopus 로고    scopus 로고
    • Molecular cloning and expression of endo-beta-N-acetylglucosaminidase D, which acts on the core structure of complex type asparagine-linked oligosaccharides
    • COI: 1:CAS:528:DC%2BD3MXls1SgsLo%3D, PID: 11388907
    • Muramatsu H, Tachikui H, Ushida H, Song X, Qiu Y, Yamamoto S, Muramatsu T (2001) Molecular cloning and expression of endo-beta-N-acetylglucosaminidase D, which acts on the core structure of complex type asparagine-linked oligosaccharides. J Biochem 129:923–928
    • (2001) J Biochem , vol.129 , pp. 923-928
    • Muramatsu, H.1    Tachikui, H.2    Ushida, H.3    Song, X.4    Qiu, Y.5    Yamamoto, S.6    Muramatsu, T.7
  • 83
    • 28444495153 scopus 로고    scopus 로고
    • IgG subclass-independent improvement of antibody-dependent cellular cytotoxicity by fucose removal from Asn297-linked oligosaccharides
    • COI: 1:CAS:528:DC%2BD2MXhtlSjt7%2FK, PID: 16219319
    • Niwa R, Natsume A, Uehara A, Wakitani M, Iida S, Uchida K, Satoh M, Shitara K (2005) IgG subclass-independent improvement of antibody-dependent cellular cytotoxicity by fucose removal from Asn297-linked oligosaccharides. J Immunol Methods 306:151–160
    • (2005) J Immunol Methods , vol.306 , pp. 151-160
    • Niwa, R.1    Natsume, A.2    Uehara, A.3    Wakitani, M.4    Iida, S.5    Uchida, K.6    Satoh, M.7    Shitara, K.8
  • 84
    • 84867700072 scopus 로고    scopus 로고
    • A practical one-step synthesis of 1,2-oxazoline derivatives from unprotected sugars and its application to chemoenzymatic beta-N-acetylglucosaminidation of disialo-oligosaccharide
    • COI: 1:CAS:528:DC%2BC38XhsFChtb7E
    • Noguchi M, Fujieda T, Huang WC, Ishihara M, Kobayashi A, Shoda S-I (2012) A practical one-step synthesis of 1,2-oxazoline derivatives from unprotected sugars and its application to chemoenzymatic beta-N-acetylglucosaminidation of disialo-oligosaccharide. Helv. Chim. Acta 95:1928–1936
    • (2012) Helv. Chim. Acta , vol.95 , pp. 1928-1936
    • Noguchi, M.1    Fujieda, T.2    Huang, W.C.3    Ishihara, M.4    Kobayashi, A.5    Shoda, S.-I.6
  • 85
    • 62349129117 scopus 로고    scopus 로고
    • Efficient synthesis of sugar oxazolines from unprotected N-acetyl-2-amino sugars by using chloroformamidinium reagent in water
    • COI: 1:CAS:528:DC%2BD1MXhs1Slsrc%3D, PID: 19203234
    • Noguchi M, Tanaka T, Gyakushi H, Kobayashi A, Shoda S (2009) Efficient synthesis of sugar oxazolines from unprotected N-acetyl-2-amino sugars by using chloroformamidinium reagent in water. J Org Chem 74:2210–2212
    • (2009) J Org Chem , vol.74 , pp. 2210-2212
    • Noguchi, M.1    Tanaka, T.2    Gyakushi, H.3    Kobayashi, A.4    Shoda, S.5
  • 86
    • 0021041854 scopus 로고
    • Biological significance of carbohydrate chains on monoclonal antibodies
    • COI: 1:CAS:528:DyaL3sXmtFSqtro%3D, PID: 6579549
    • Nose M, Wigzell H (1983) Biological significance of carbohydrate chains on monoclonal antibodies. Proc Natl Acad Sci USA 80:6632–6636
    • (1983) Proc Natl Acad Sci USA , vol.80 , pp. 6632-6636
    • Nose, M.1    Wigzell, H.2
  • 87
    • 1242317024 scopus 로고    scopus 로고
    • Fucose depletion from human IgG1 oligosaccharide enhances binding enthalpy and association rate between IgG1 and FcgammaRIIIa
    • COI: 1:CAS:528:DC%2BD2cXht1Kiu7g%3D, PID: 15037082
    • Okazaki A, Shoji-Hosaka E, Nakamura K, Wakitani M, Uchida K, Kakita S, Tsumoto K, Kumagai I, Shitara K (2004) Fucose depletion from human IgG1 oligosaccharide enhances binding enthalpy and association rate between IgG1 and FcgammaRIIIa. J Mol Biol 336:1239–1249
    • (2004) J Mol Biol , vol.336 , pp. 1239-1249
    • Okazaki, A.1    Shoji-Hosaka, E.2    Nakamura, K.3    Wakitani, M.4    Uchida, K.5    Kakita, S.6    Tsumoto, K.7    Kumagai, I.8    Shitara, K.9
  • 89
    • 0002121160 scopus 로고
    • X-ray diffraction studies of antibody constant regions
    • Metzger H, (ed), American Society for Microbiology, Washington, DC
    • Padlan EA (1990) X-ray diffraction studies of antibody constant regions. In: Metzger H (ed) Fc receptors and the action of antibodies. American Society for Microbiology, Washington, DC, pp 12–30
    • (1990) Fc receptors and the action of antibodies , pp. 12-30
    • Padlan, E.A.1
  • 90
    • 0027450137 scopus 로고
    • Aglycosylated chimaeric human IgG3 can trigger the human phagocyte respiratory burst
    • COI: 1:CAS:528:DyaK3sXhvV2ksbc%3D, PID: 8381917
    • Pound JD, Lund J, Jefferis R (1993) Aglycosylated chimaeric human IgG3 can trigger the human phagocyte respiratory burst. Mol Immunol 30:233–241
    • (1993) Mol Immunol , vol.30 , pp. 233-241
    • Pound, J.D.1    Lund, J.2    Jefferis, R.3
  • 92
    • 33947688082 scopus 로고    scopus 로고
    • Structural characterization of N-linked oligosaccharides on monoclonal antibody cetuximab by the combination of orthogonal matrix-assisted laser desorption/ionization hybrid quadrupole–quadrupole time-of-flight tandem mass spectrometry and sequential enzymatic digestion
    • COI: 1:CAS:528:DC%2BD2sXjslSmu7s%3D, PID: 17362871
    • Qian J, Liu T, Yang L, Daus A, Crowley R, Zhou Q (2007) Structural characterization of N-linked oligosaccharides on monoclonal antibody cetuximab by the combination of orthogonal matrix-assisted laser desorption/ionization hybrid quadrupole–quadrupole time-of-flight tandem mass spectrometry and sequential enzymatic digestion. Anal Biochem 364:8–18
    • (2007) Anal Biochem , vol.364 , pp. 8-18
    • Qian, J.1    Liu, T.2    Yang, L.3    Daus, A.4    Crowley, R.5    Zhou, Q.6
  • 94
    • 0035844212 scopus 로고    scopus 로고
    • The structure of a human type III Fcgamma receptor in complex with Fc
    • COI: 1:CAS:528:DC%2BD3MXjvFarsrw%3D, PID: 11297532
    • Radaev S, Motyka S, Fridman WH, Sautes-Fridman C, Sun PD (2001) The structure of a human type III Fcgamma receptor in complex with Fc. J Biol Chem 276:16469–16477
    • (2001) J Biol Chem , vol.276 , pp. 16469-16477
    • Radaev, S.1    Motyka, S.2    Fridman, W.H.3    Sautes-Fridman, C.4    Sun, P.D.5
  • 96
    • 0034050074 scopus 로고    scopus 로고
    • Species-specific variation in glycosylation of IgG: evidence for the species-specific sialylation and branch-specific galactosylation and importance for engineering recombinant glycoprotein therapeutics
    • COI: 1:CAS:528:DC%2BD3cXislSmu7s%3D, PID: 10764836
    • Raju TS, Briggs JB, Borge SM, Jones AJ (2000) Species-specific variation in glycosylation of IgG: evidence for the species-specific sialylation and branch-specific galactosylation and importance for engineering recombinant glycoprotein therapeutics. Glycobiology 10:477–486
    • (2000) Glycobiology , vol.10 , pp. 477-486
    • Raju, T.S.1    Briggs, J.B.2    Borge, S.M.3    Jones, A.J.4
  • 97
    • 84940644112 scopus 로고    scopus 로고
    • Production of alpha2,6-sialylated IgG1 in CHO cells
    • COI: 1:CAS:528:DC%2BC28XmvFyqs7g%3D, PID: 25875452
    • Raymond C, Robotham A, Spearman M, Butler M, Kelly J, Durocher Y (2015) Production of alpha2,6-sialylated IgG1 in CHO cells. MAbs 7:571–583
    • (2015) MAbs , vol.7 , pp. 571-583
    • Raymond, C.1    Robotham, A.2    Spearman, M.3    Butler, M.4    Kelly, J.5    Durocher, Y.6
  • 98
    • 34548229364 scopus 로고    scopus 로고
    • FcRn: the neonatal Fc receptor comes of age
    • COI: 1:CAS:528:DC%2BD2sXpsV2qtbw%3D, PID: 17703228
    • Roopenian DC, Akilesh S (2007) FcRn: the neonatal Fc receptor comes of age. Nat Rev Immunol 7:715–725
    • (2007) Nat Rev Immunol , vol.7 , pp. 715-725
    • Roopenian, D.C.1    Akilesh, S.2
  • 99
    • 34447310112 scopus 로고    scopus 로고
    • Detailed structural analysis of N-glycans released from glycoproteins in SDS-PAGE gel bands using HPLC combined with exoglycosidase array digestions
    • COI: 1:CAS:528:DC%2BD28Xht1ersrvK, PID: 17072008
    • Royle L, Radcliffe CM, Dwek RA, Rudd PM (2006) Detailed structural analysis of N-glycans released from glycoproteins in SDS-PAGE gel bands using HPLC combined with exoglycosidase array digestions. Methods Mol Biol 347:125–143
    • (2006) Methods Mol Biol , vol.347 , pp. 125-143
    • Royle, L.1    Radcliffe, C.M.2    Dwek, R.A.3    Rudd, P.M.4
  • 100
    • 0030937062 scopus 로고    scopus 로고
    • Glycosylation: heterogeneity and the 3D structure of proteins
    • COI: 1:CAS:528:DyaK2sXhvFKgsbw%3D, PID: 9063619
    • Rudd PM, Dwek RA (1997) Glycosylation: heterogeneity and the 3D structure of proteins. Crit Rev Biochem Mol Biol 32:1–100
    • (1997) Crit Rev Biochem Mol Biol , vol.32 , pp. 1-100
    • Rudd, P.M.1    Dwek, R.A.2
  • 101
    • 0026507779 scopus 로고
    • Mapping and comparison of the interaction sites on the Fc region of IgG responsible for triggering antibody dependent cellular cytotoxicity (ADCC) through different types of human Fc gamma receptor
    • COI: 1:CAS:528:DyaK38XktVGkt7w%3D, PID: 1533898
    • Sarmay G, Lund J, Rozsnyay Z, Gergely J, Jefferis R (1992) Mapping and comparison of the interaction sites on the Fc region of IgG responsible for triggering antibody dependent cellular cytotoxicity (ADCC) through different types of human Fc gamma receptor. Mol Immunol 29:633–639
    • (1992) Mol Immunol , vol.29 , pp. 633-639
    • Sarmay, G.1    Lund, J.2    Rozsnyay, Z.3    Gergely, J.4    Jefferis, R.5
  • 102
    • 58149510052 scopus 로고    scopus 로고
    • Aglycosylated immunoglobulin G1 variants productively engage activating Fc receptors
    • COI: 1:CAS:528:DC%2BD1MXhsFWgtw%3D%3D, PID: 19074274
    • Sazinsky SL, Ott RG, Silver NW, Tidor B, Ravetch JV, Wittrup KD (2008) Aglycosylated immunoglobulin G1 variants productively engage activating Fc receptors. Proc Natl Acad Sci USA 105:20167–20172
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 20167-20172
    • Sazinsky, S.L.1    Ott, R.G.2    Silver, N.W.3    Tidor, B.4    Ravetch, J.V.5    Wittrup, K.D.6
  • 103
    • 33751253486 scopus 로고    scopus 로고
    • Higher levels of sialylated Fc glycans in immunoglobulin G molecules can adversely impact functionality
    • COI: 1:CAS:528:DC%2BD28Xht1ems7zJ, PID: 17045339
    • Scallon BJ, Tam SH, McCarthy SG, Cai AN, Raju TS (2007) Higher levels of sialylated Fc glycans in immunoglobulin G molecules can adversely impact functionality. Mol Immunol 44:1524–1534
    • (2007) Mol Immunol , vol.44 , pp. 1524-1534
    • Scallon, B.J.1    Tam, S.H.2    McCarthy, S.G.3    Cai, A.N.4    Raju, T.S.5
  • 104
    • 84861830510 scopus 로고    scopus 로고
    • A phase 1 study of obinutuzumab induction followed by 2 years of maintenance in patients with relapsed CD20-positive B-cell malignancies
    • COI: 1:CAS:528:DC%2BC38XhtVWjsrfN, PID: 22438256
    • Sehn LH, Assouline SE, Stewart DA, Mangel J, Gascoyne RD, Fine G, Frances-Lasserre S, Carlile DJ, Crump M (2012) A phase 1 study of obinutuzumab induction followed by 2 years of maintenance in patients with relapsed CD20-positive B-cell malignancies. Blood 119:5118–5125
    • (2012) Blood , vol.119 , pp. 5118-5125
    • Sehn, L.H.1    Assouline, S.E.2    Stewart, D.A.3    Mangel, J.4    Gascoyne, R.D.5    Fine, G.6    Frances-Lasserre, S.7    Carlile, D.J.8    Crump, M.9
  • 105
    • 84944960445 scopus 로고    scopus 로고
    • Randomized phase II trial comparing obinutuzumab (GA101) with rituximab in patients with relapsed CD20 + indolent B-Cell non-Hodgkin lymphoma: final analysis of the GAUSS study
    • COI: 1:CAS:528:DC%2BC28XmvVynt74%3D, PID: 26282650
    • Sehn LH, Goy A, Offner FC, Martinelli G, Caballero MD, Gadeberg O, Baetz T, Zelenetz AD, Gaidano G, Fayad LE et al (2015) Randomized phase II trial comparing obinutuzumab (GA101) with rituximab in patients with relapsed CD20 + indolent B-Cell non-Hodgkin lymphoma: final analysis of the GAUSS study. J Clin Oncol 33:3467–3474
    • (2015) J Clin Oncol , vol.33 , pp. 3467-3474
    • Sehn, L.H.1    Goy, A.2    Offner, F.C.3    Martinelli, G.4    Caballero, M.D.5    Gadeberg, O.6    Baetz, T.7    Zelenetz, A.D.8    Gaidano, G.9    Fayad, L.E.10
  • 106
    • 58149343570 scopus 로고    scopus 로고
    • The N-linked oligosaccharide at Fc gamma RIIIa Asn-45: an inhibitory element for high Fc gamma RIIIa binding affinity to IgG glycoforms lacking core fucosylation
    • COI: 1:CAS:528:DC%2BD1MXmvVym, PID: 18952826
    • Shibata-Koyama M, Iida S, Okazaki A, Mori K, Kitajima-Miyama K, Saitou S, Kakita S, Kanda Y, Shitara K, Kato K et al (2009) The N-linked oligosaccharide at Fc gamma RIIIa Asn-45: an inhibitory element for high Fc gamma RIIIa binding affinity to IgG glycoforms lacking core fucosylation. Glycobiology 19:126–134
    • (2009) Glycobiology , vol.19 , pp. 126-134
    • Shibata-Koyama, M.1    Iida, S.2    Okazaki, A.3    Mori, K.4    Kitajima-Miyama, K.5    Saitou, S.6    Kakita, S.7    Kanda, Y.8    Shitara, K.9    Kato, K.10
  • 107
    • 0037178791 scopus 로고    scopus 로고
    • Lack of fucose on human IgG1N-linked oligosaccharide improves binding to human Fcgamma RIII and antibody-dependent cellular toxicity
    • COI: 1:CAS:528:DC%2BD38XlvV2isrk%3D, PID: 11986321
    • Shields RL, Lai J, Keck R, O’Connell LY, Hong K, Meng YG, Weikert SH, Presta LG (2002) Lack of fucose on human IgG1N-linked oligosaccharide improves binding to human Fcgamma RIII and antibody-dependent cellular toxicity. J Biol Chem 277:26733–26740
    • (2002) J Biol Chem , vol.277 , pp. 26733-26740
    • Shields, R.L.1    Lai, J.2    Keck, R.3    O’Connell, L.Y.4    Hong, K.5    Meng, Y.G.6    Weikert, S.H.7    Presta, L.G.8
  • 108
    • 0035794194 scopus 로고    scopus 로고
    • High resolution mapping of the binding site on human IgG1 for Fc gamma RI, Fc gamma RII, Fc gamma RIII, and FcRn and design of IgG1 variants with improved binding to the Fc gamma R
    • COI: 1:CAS:528:DC%2BD3MXhslShurs%3D, PID: 11096108
    • Shields RL, Namenuk AK, Hong K, Meng YG, Rae J, Briggs J, Xie D, Lai J, Stadlen A, Li B et al (2001) High resolution mapping of the binding site on human IgG1 for Fc gamma RI, Fc gamma RII, Fc gamma RIII, and FcRn and design of IgG1 variants with improved binding to the Fc gamma R. J Biol Chem 276:6591–6604
    • (2001) J Biol Chem , vol.276 , pp. 6591-6604
    • Shields, R.L.1    Namenuk, A.K.2    Hong, K.3    Meng, Y.G.4    Rae, J.5    Briggs, J.6    Xie, D.7    Lai, J.8    Stadlen, A.9    Li, B.10
  • 109
    • 0037474276 scopus 로고    scopus 로고
    • The absence of fucose but not the presence of galactose or bisecting N-acetylglucosamine of human IgG1 complex-type oligosaccharides shows the critical role of enhancing antibody-dependent cellular cytotoxicity
    • COI: 1:CAS:528:DC%2BD3sXmt1Kiuw%3D%3D, PID: 12427744
    • Shinkawa T, Nakamura K, Yamane N, Shoji-Hosaka E, Kanda Y, Sakurada M, Uchida K, Anazawa H, Satoh M, Yamasaki M et al (2003) The absence of fucose but not the presence of galactose or bisecting N-acetylglucosamine of human IgG1 complex-type oligosaccharides shows the critical role of enhancing antibody-dependent cellular cytotoxicity. J Biol Chem 278:3466–3473
    • (2003) J Biol Chem , vol.278 , pp. 3466-3473
    • Shinkawa, T.1    Nakamura, K.2    Yamane, N.3    Shoji-Hosaka, E.4    Kanda, Y.5    Sakurada, M.6    Uchida, K.7    Anazawa, H.8    Satoh, M.9    Yamasaki, M.10
  • 110
  • 111
    • 0033106166 scopus 로고    scopus 로고
    • Crystal structure of the soluble form of the human fcgamma-receptor IIb: a new member of the immunoglobulin superfamily at 1.7 A resolution
    • COI: 1:CAS:528:DyaK1MXhvFOltLc%3D, PID: 10064577
    • Sondermann P, Huber R, Jacob U (1999) Crystal structure of the soluble form of the human fcgamma-receptor IIb: a new member of the immunoglobulin superfamily at 1.7 A resolution. EMBO J 18:1095–1103
    • (1999) EMBO J , vol.18 , pp. 1095-1103
    • Sondermann, P.1    Huber, R.2    Jacob, U.3
  • 112
    • 0034691322 scopus 로고    scopus 로고
    • The 3.2-A crystal structure of the human IgG1 Fc fragment-Fc gammaRIII complex
    • COI: 1:CAS:528:DC%2BD3cXlsFKisro%3D, PID: 10917521
    • Sondermann P, Huber R, Oosthuizen V, Jacob U (2000) The 3.2-A crystal structure of the human IgG1 Fc fragment-Fc gammaRIII complex. Nature 406:267–273
    • (2000) Nature , vol.406 , pp. 267-273
    • Sondermann, P.1    Huber, R.2    Oosthuizen, V.3    Jacob, U.4
  • 113
    • 0032586977 scopus 로고    scopus 로고
    • Human Fcgamma receptor IIb expressed in Escherichia coli reveals IgG binding capability
    • COI: 1:CAS:528:DyaK1MXksVWgu78%3D, PID: 10430038
    • Sondermann P, Jacob U (1999) Human Fcgamma receptor IIb expressed in Escherichia coli reveals IgG binding capability. Biol Chem 380:717–721
    • (1999) Biol Chem , vol.380 , pp. 717-721
    • Sondermann, P.1    Jacob, U.2
  • 114
    • 84906097052 scopus 로고    scopus 로고
    • A simplified procedure for gram-scale production of sialylglycopeptide (SGP) from egg yolks and subsequent semi-synthesis of Man3GlcNAc oxazoline
    • COI: 1:CAS:528:DC%2BC2cXhtlKkt7fP, PID: 25124522
    • Sun B, Bao W, Tian X, Li M, Liu H, Dong J, Huang W (2014) A simplified procedure for gram-scale production of sialylglycopeptide (SGP) from egg yolks and subsequent semi-synthesis of Man3GlcNAc oxazoline. Carbohydr Res 396:62–69
    • (2014) Carbohydr Res , vol.396 , pp. 62-69
    • Sun, B.1    Bao, W.2    Tian, X.3    Li, M.4    Liu, H.5    Dong, J.6    Huang, W.7
  • 115
    • 0028843229 scopus 로고
    • Synthesis of neoglycoproteins using oligosaccharide-transfer activity with endo-beta-N-acetylglucosaminidase
    • COI: 1:CAS:528:DyaK2MXjslahtbw%3D, PID: 7852391
    • Takegawa K, Tabuchi M, Yamaguchi S, Kondo A, Kato I, Iwahara S (1995) Synthesis of neoglycoproteins using oligosaccharide-transfer activity with endo-beta-N-acetylglucosaminidase. J Biol Chem 270:3094–3099
    • (1995) J Biol Chem , vol.270 , pp. 3094-3099
    • Takegawa, K.1    Tabuchi, M.2    Yamaguchi, S.3    Kondo, A.4    Kato, I.5    Iwahara, S.6
  • 116
    • 0031005483 scopus 로고    scopus 로고
    • Cloning, sequencing, and expression of Arthrobacter protophormiae endo-beta-N-acetylglucosaminidase in Escherichia coli
    • COI: 1:CAS:528:DyaK2sXotFWmuw%3D%3D, PID: 9015383
    • Takegawa K, Yamabe K, Fujita K, Tabuchi M, Mita M, Izu H, Watanabe A, Asada Y, Sano M, Kondo A et al (1997) Cloning, sequencing, and expression of Arthrobacter protophormiae endo-beta-N-acetylglucosaminidase in Escherichia coli. Arch Biochem Biophys 338:22–28
    • (1997) Arch Biochem Biophys , vol.338 , pp. 22-28
    • Takegawa, K.1    Yamabe, K.2    Fujita, K.3    Tabuchi, M.4    Mita, M.5    Izu, H.6    Watanabe, A.7    Asada, Y.8    Sano, M.9    Kondo, A.10
  • 117
    • 0023849601 scopus 로고
    • Comparative study of the asparagine-linked sugar chains of human erythropoietins purified from urine and the culture medium of recombinant Chinese hamster ovary cells
    • COI: 1:CAS:528:DyaL1cXitFKntrg%3D, PID: 3346214
    • Takeuchi M, Takasaki S, Miyazaki H, Kato T, Hoshi S, Kochibe N, Kobata A (1988) Comparative study of the asparagine-linked sugar chains of human erythropoietins purified from urine and the culture medium of recombinant Chinese hamster ovary cells. J Biol Chem 263:3657–3663
    • (1988) J Biol Chem , vol.263 , pp. 3657-3663
    • Takeuchi, M.1    Takasaki, S.2    Miyazaki, H.3    Kato, T.4    Hoshi, S.5    Kochibe, N.6    Kobata, A.7
  • 119
    • 0024438061 scopus 로고
    • Studies of aglycosylated chimeric mouse-human IgG. Role of carbohydrate in the structure and effector functions mediated by the human IgG constant region
    • COI: 1:CAS:528:DyaL1MXmtFejtrs%3D, PID: 2507634
    • Tao MH, Morrison SL (1989) Studies of aglycosylated chimeric mouse-human IgG. Role of carbohydrate in the structure and effector functions mediated by the human IgG constant region. J Immunol 143:2595–2601
    • (1989) J Immunol , vol.143 , pp. 2595-2601
    • Tao, M.H.1    Morrison, S.L.2
  • 120
    • 84886806068 scopus 로고    scopus 로고
    • Intravenous immunoglobulin expands regulatory T cells via induction of cyclooxygenase-2-dependent prostaglandin E2 in human dendritic cells
    • COI: 1:CAS:528:DC%2BC3sXhsVSqu73J, PID: 23847198
    • Trinath J, Hegde P, Sharma M, Maddur MS, Rabin M, Vallat JM, Magy L, Balaji KN, Kaveri SV, Bayry J (2013) Intravenous immunoglobulin expands regulatory T cells via induction of cyclooxygenase-2-dependent prostaglandin E2 in human dendritic cells. Blood 122:1419–1427
    • (2013) Blood , vol.122 , pp. 1419-1427
    • Trinath, J.1    Hegde, P.2    Sharma, M.3    Maddur, M.S.4    Rabin, M.5    Vallat, J.M.6    Magy, L.7    Balaji, K.N.8    Kaveri, S.V.9    Bayry, J.10
  • 121
    • 0033044588 scopus 로고    scopus 로고
    • Engineered glycoforms of an antineuroblastoma IgG1 with optimized antibody-dependent cellular cytotoxic activity
    • COI: 1:CAS:528:DyaK1MXpsl2ktw%3D%3D, PID: 10052355
    • Umana P, Jean-Mairet J, Moudry R, Amstutz H, Bailey JE (1999) Engineered glycoforms of an antineuroblastoma IgG1 with optimized antibody-dependent cellular cytotoxic activity. Nat Biotechnol 17:176–180
    • (1999) Nat Biotechnol , vol.17 , pp. 176-180
    • Umana, P.1    Jean-Mairet, J.2    Moudry, R.3    Amstutz, H.4    Bailey, J.E.5
  • 122
    • 73649089287 scopus 로고    scopus 로고
    • Efficient glycosynthase mutant derived from Mucor hiemalis endo-beta-N-acetylglucosaminidase capable of transferring oligosaccharide from both sugar oxazoline and natural N-glycan
    • COI: 1:CAS:528:DC%2BD1MXhs1Sqtr%2FL, PID: 19880511
    • Umekawa M, Li C, Higashiyama T, Huang W, Ashida H, Yamamoto K, Wang LX (2010) Efficient glycosynthase mutant derived from Mucor hiemalis endo-beta-N-acetylglucosaminidase capable of transferring oligosaccharide from both sugar oxazoline and natural N-glycan. J Biol Chem 285:511–521
    • (2010) J Biol Chem , vol.285 , pp. 511-521
    • Umekawa, M.1    Li, C.2    Higashiyama, T.3    Huang, W.4    Ashida, H.5    Yamamoto, K.6    Wang, L.X.7
  • 123
    • 0019322927 scopus 로고
    • Specificity in the enzymic transfer of sialic acid to the oligosaccharide branches of b1- and triantennary glycopeptides of alpha 1-acid glycoprotein
    • PID: 6767476
    • van den Eijnden DH, Joziasse DH, Dorland L, van Halbeek H, Vliegenthart JF, Schmid K (1980) Specificity in the enzymic transfer of sialic acid to the oligosaccharide branches of b1- and triantennary glycopeptides of alpha 1-acid glycoprotein. Biochem Biophys Res Commun 92:839–845
    • (1980) Biochem Biophys Res Commun , vol.92 , pp. 839-845
    • van den Eijnden, D.H.1    Joziasse, D.H.2    Dorland, L.3    van Halbeek, H.4    Vliegenthart, J.F.5    Schmid, K.6
  • 124
    • 85018510445 scopus 로고    scopus 로고
    • Population pharmacokinetics and pharmacodynamics of benralizumab in healthy volunteers and patients with asthma
    • COI: 1:CAS:528:DC%2BC2sXhtlehsrw%3D
    • Wang B, Yan L, Yao Z, Roskos LK (2017) Population pharmacokinetics and pharmacodynamics of benralizumab in healthy volunteers and patients with asthma. CPT Pharmacomet Syst Pharmacol. 6(4):249–257
    • (2017) CPT Pharmacomet Syst Pharmacol , vol.6 , Issue.4 , pp. 249-257
    • Wang, B.1    Yan, L.2    Yao, Z.3    Roskos, L.K.4
  • 125
    • 52949115690 scopus 로고    scopus 로고
    • Glycoengineering of human IgG1-Fc through combined yeast expression and in vitro chemoenzymatic glycosylation
    • COI: 1:CAS:528:DC%2BD1cXhtVOmtrjF, PID: 18771295
    • Wei Y, Li C, Huang W, Li B, Strome S, Wang LX (2008) Glycoengineering of human IgG1-Fc through combined yeast expression and in vitro chemoenzymatic glycosylation. Biochemistry 47:10294–10304
    • (2008) Biochemistry , vol.47 , pp. 10294-10304
    • Wei, Y.1    Li, C.2    Huang, W.3    Li, B.4    Strome, S.5    Wang, L.X.6
  • 126
    • 1142298744 scopus 로고    scopus 로고
    • Human antibody-Fc receptor interactions illuminated by crystal structures
    • COI: 1:CAS:528:DC%2BD2cXksl2gtg%3D%3D, PID: 15040582
    • Woof JM, Burton DR (2004) Human antibody-Fc receptor interactions illuminated by crystal structures. Nat Rev Immunol 4:89–99
    • (2004) Nat Rev Immunol , vol.4 , pp. 89-99
    • Woof, J.M.1    Burton, D.R.2
  • 127
    • 0025909201 scopus 로고
    • Antibody variable region glycosylation: position effects on antigen binding and carbohydrate structure
    • COI: 1:CAS:528:DyaK3MXmtVGmtLw%3D, PID: 1717254
    • Wright A, Tao MH, Kabat EA, Morrison SL (1991) Antibody variable region glycosylation: position effects on antigen binding and carbohydrate structure. EMBO J 10:2717–2723
    • (1991) EMBO J , vol.10 , pp. 2717-2723
    • Wright, A.1    Tao, M.H.2    Kabat, E.A.3    Morrison, S.L.4
  • 128
    • 0030611089 scopus 로고    scopus 로고
    • A novel polymorphism of FcgammaRIIIa (CD16) alters receptor function and predisposes to autoimmune disease
    • COI: 1:CAS:528:DyaK2sXlvFOgs7k%3D, PID: 9276722
    • Wu J, Edberg JC, Redecha PB, Bansal V, Guyre PM, Coleman K, Salmon JE, Kimberly RP (1997) A novel polymorphism of FcgammaRIIIa (CD16) alters receptor function and predisposes to autoimmune disease. J Clin Invest 100:1059–1070
    • (1997) J Clin Invest , vol.100 , pp. 1059-1070
    • Wu, J.1    Edberg, J.C.2    Redecha, P.B.3    Bansal, V.4    Guyre, P.M.5    Coleman, K.6    Salmon, J.E.7    Kimberly, R.P.8
  • 130
    • 33646105366 scopus 로고    scopus 로고
    • Glycoform-dependent conformational alteration of the Fc region of human immunoglobulin G1 as revealed by NMR spectroscopy
    • COI: 1:CAS:528:DC%2BD28Xjsl2mtrY%3D, PID: 16343775
    • Yamaguchi Y, Nishimura M, Nagano M, Yagi H, Sasakawa H, Uchida K, Shitara K, Kato K (2006) Glycoform-dependent conformational alteration of the Fc region of human immunoglobulin G1 as revealed by NMR spectroscopy. Biochim Biophys Acta 1760:693–700
    • (2006) Biochim Biophys Acta , vol.1760 , pp. 693-700
    • Yamaguchi, Y.1    Nishimura, M.2    Nagano, M.3    Yagi, H.4    Sasakawa, H.5    Uchida, K.6    Shitara, K.7    Kato, K.8
  • 131
    • 85007998573 scopus 로고
    • Novel specificities of Mucor hiemalis endo-beta-N-acetylglucosaminidase acting complex asparagine-linked oligosaccharides
    • COI: 1:CAS:528:DyaK2cXhvVGqtro%3D, PID: 7509658
    • Yamamoto K, Kadowaki S, Fujisaki M, Kumagai H, Tochikura T (1994) Novel specificities of Mucor hiemalis endo-beta-N-acetylglucosaminidase acting complex asparagine-linked oligosaccharides. Biosci Biotechnol Biochem 58:72–77
    • (1994) Biosci Biotechnol Biochem , vol.58 , pp. 72-77
    • Yamamoto, K.1    Kadowaki, S.2    Fujisaki, M.3    Kumagai, H.4    Tochikura, T.5
  • 132
    • 77951916883 scopus 로고    scopus 로고
    • Phase I study of KW-0761, a defucosylated humanized anti-CCR4 antibody, in relapsed patients with adult T-cell leukemia-lymphoma and peripheral T-cell lymphoma
    • COI: 1:CAS:528:DC%2BC3cXltFGht7w%3D, PID: 20177026
    • Yamamoto K, Utsunomiya A, Tobinai K, Tsukasaki K, Uike N, Uozumi K, Yamaguchi K, Yamada Y, Hanada S, Tamura K et al (2010) Phase I study of KW-0761, a defucosylated humanized anti-CCR4 antibody, in relapsed patients with adult T-cell leukemia-lymphoma and peripheral T-cell lymphoma. J Clin Oncol 28:1591–1598
    • (2010) J Clin Oncol , vol.28 , pp. 1591-1598
    • Yamamoto, K.1    Utsunomiya, A.2    Tobinai, K.3    Tsukasaki, K.4    Uike, N.5    Uozumi, K.6    Yamaguchi, K.7    Yamada, Y.8    Hanada, S.9    Tamura, K.10
  • 133
    • 4644245850 scopus 로고    scopus 로고
    • Establishment of FUT8 knockout Chinese hamster ovary cells: an ideal host cell line for producing completely defucosylated antibodies with enhanced antibody-dependent cellular cytotoxicity
    • COI: 1:CAS:528:DC%2BD2cXnt1Wjtb8%3D, PID: 15352059
    • Yamane-Ohnuki N, Kinoshita S, Inoue-Urakubo M, Kusunoki M, Iida S, Nakano R, Wakitani M, Niwa R, Sakurada M, Uchida K et al (2004) Establishment of FUT8 knockout Chinese hamster ovary cells: an ideal host cell line for producing completely defucosylated antibodies with enhanced antibody-dependent cellular cytotoxicity. Biotechnol Bioeng 87:614–622
    • (2004) Biotechnol Bioeng , vol.87 , pp. 614-622
    • Yamane-Ohnuki, N.1    Kinoshita, S.2    Inoue-Urakubo, M.3    Kusunoki, M.4    Iida, S.5    Nakano, R.6    Wakitani, M.7    Niwa, R.8    Sakurada, M.9    Uchida, K.10
  • 134
    • 84875749746 scopus 로고    scopus 로고
    • Dissecting the molecular mechanism of IVIg therapy: the interaction between serum IgG and DC-SIGN is independent of antibody glycoform or Fc domain
    • COI: 1:CAS:528:DC%2BC3sXjvFCgu74%3D, PID: 23416198
    • Yu X, Vasiljevic S, Mitchell DA, Crispin M, Scanlan CN (2013) Dissecting the molecular mechanism of IVIg therapy: the interaction between serum IgG and DC-SIGN is independent of antibody glycoform or Fc domain. J Mol Biol 425:1253–1258
    • (2013) J Mol Biol , vol.425 , pp. 1253-1258
    • Yu, X.1    Vasiljevic, S.2    Mitchell, D.A.3    Crispin, M.4    Scanlan, C.N.5
  • 135
    • 84957922718 scopus 로고    scopus 로고
    • Challenges of glycosylation analysis and control: an integrated approach to producing optimal and consistent therapeutic drugs
    • COI: 1:CAS:528:DC%2BC28XhvFSkurk%3D, PID: 26821133
    • Zhang P, Woen S, Wang T, Liau B, Zhao S, Chen C, Yang Y, Song Z, Wormald MR, Yu C et al (2016) Challenges of glycosylation analysis and control: an integrated approach to producing optimal and consistent therapeutic drugs. Drug Discov Today 21:740–765
    • (2016) Drug Discov Today , vol.21 , pp. 740-765
    • Zhang, P.1    Woen, S.2    Wang, T.3    Liau, B.4    Zhao, S.5    Chen, C.6    Yang, Y.7    Song, Z.8    Wormald, M.R.9    Yu, C.10
  • 136
    • 0036872920 scopus 로고    scopus 로고
    • Anti-N-glycolylneuraminic acid antibodies identified in healthy human serum
    • PID: 12371933
    • Zhu A, Hurst R (2002) Anti-N-glycolylneuraminic acid antibodies identified in healthy human serum. Xenotransplantation 9:376–381
    • (2002) Xenotransplantation , vol.9 , pp. 376-381
    • Zhu, A.1    Hurst, R.2


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