메뉴 건너뛰기




Volumn 34, Issue SUPPL. 1, 2014, Pages

Fc glycan-modulated immunoglobulin G effector functions

Author keywords

CIDP; Fc; IgG; IVIG; Sialic acid

Indexed keywords

FC RECEPTOR; FUCOSE; GALACTOSE; GLYCAN; IMMUNOGLOBULIN FC FRAGMENT; IMMUNOGLOBULIN G; SIALIC ACID; IMMUNOGLOBULIN; N ACETYLNEURAMINIC ACID; POLYSACCHARIDE; PROTEIN BINDING;

EID: 84905090765     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-014-0018-3     Document Type: Article
Times cited : (50)

References (59)
  • 2
    • 84877152391 scopus 로고    scopus 로고
    • Natural variation in Fc glycosylation of HIV-specific antibodies impacts antiviral activity
    • Ackerman ME, Crispin M, Yu X, Baruah K, Boesch AW, Harvey DJ, et al. Natural variation in Fc glycosylation of HIV-specific antibodies impacts antiviral activity. J Clin Invest. 2013;123:2183-92.
    • (2013) J Clin Invest , vol.123 , pp. 2183-2192
    • Ackerman, M.E.1    Crispin, M.2    Yu, X.3    Baruah, K.4    Boesch, A.W.5    Harvey, D.J.6
  • 3
    • 0001644020 scopus 로고    scopus 로고
    • The human plasma proteome: History, character, and diagnostic prospects
    • Anderson NL, Anderson NG. The human plasma proteome: history, character, and diagnostic prospects. Mol Cell Proteomics. 2002;1:845-67.
    • (2002) Mol Cell Proteomics , vol.1 , pp. 845-867
    • Anderson, N.L.1    Anderson, N.G.2
  • 4
    • 79960046406 scopus 로고    scopus 로고
    • Intravenous gammaglobulin suppresses inflammation through a novel T(H)2 pathway
    • Anthony RM, Kobayashi T, Wermeling F, Ravetch JV. Intravenous gammaglobulin suppresses inflammation through a novel T(H)2 pathway. Nature. 2011;475:110-3.
    • (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
    • DOI 10.1126/science.1154315
    • Anthony RM, Nimmerjahn F, Ashline DJ, Reinhold VN, Paulson JC, Ravetch JV. Recapitulation of IVIG anti-inflammatory activity with a recombinant IgG Fc. Science. 2008;320:373-6. (Pubitemid 351555659)
    • (2008) Science , vol.320 , Issue.5874 , 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
  • 7
    • 34247122497 scopus 로고    scopus 로고
    • The impact of glycosylation on the biological function and structure of human immunoglobulins
    • DOI 10.1146/annurev.immunol.25.022106.141702
    • Arnold JN, Wormald MR, Sim RB, Rudd PM, Dwek RA. The impact of glycosylation on the biological function and structure of human immunoglobulins. Annu Rev Immunol. 2007;25:21-50. (Pubitemid 46697901)
    • (2007) Annual Review of Immunology , 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
    • 70350055478 scopus 로고    scopus 로고
    • Branch-specific sialylation of IgG-Fc glycans by ST6Gal-I
    • Barb AW, Brady EK, Prestegard JH. Branch-specific sialylation of IgG-Fc glycans by ST6Gal-I. Biochemistry. 2009;48:9705-7.
    • (2009) Biochemistry , vol.48 , pp. 9705-9707
    • Barb, A.W.1    Brady, E.K.2    Prestegard, J.H.3
  • 10
    • 0036464719 scopus 로고    scopus 로고
    • Therapeutic activity of humanized anti-CD20 monoclonal antibody and polymorphism in IgG Fc receptor FcgammarIIIa gene
    • DOI 10.1182/blood.V99.3.754
    • Cartron G, Dacheux L, Salles G, Solal-Celigny P, Bardos P, Colombat P, et al. Therapeutic activity of humanized anti-CD20 monoclonal antibody and polymorphism in IgG Fc receptor FcgammaRIIIa gene. Blood. 2002;99:754-8. (Pubitemid 34525533)
    • (2002) Blood , vol.99 , Issue.3 , pp. 754-758
    • Cartron, G.1    Dacheux, L.2    Salles, G.3    Solal-Celigny, P.4    Bardos, P.5    Colombat, P.6    Watier, H.7
  • 13
    • 42049119909 scopus 로고    scopus 로고
    • Mannose-binding lectin deficiency is associated with early onset of polyarticular juvenile rheumatoid arthritis: A cohort study
    • Dolman KM, Brouwer N, Frakking FN, Flato B, Tak PP, Kuijpers TW, et al. Mannose-binding lectin deficiency is associated with early onset of polyarticular juvenile rheumatoid arthritis: a cohort study. Arthritis Res Ther. 2008;10:R32.
    • (2008) Arthritis Res Ther , vol.10
    • Dolman, K.M.1    Brouwer, N.2    Frakking, F.N.3    Flato, B.4    Tak, P.P.5    Kuijpers, T.W.6
  • 14
    • 0023897194 scopus 로고
    • The binding site for C1q on IgG
    • Duncan AR, Winter G. The binding site for C1q on IgG. Nature. 1988;332:738-40.
    • (1988) Nature , vol.332 , pp. 738-740
    • Duncan, A.R.1    Winter, G.2
  • 15
    • 79961233787 scopus 로고    scopus 로고
    • Unique carbohydrate-carbohydrate interactions are required for high affinity binding between FcgammaRIII and antibodies lacking core fucose
    • Ferrara C, Grau S, Jager C, Sondermann P, Brunker P, Waldhauer I, et al. Unique carbohydrate-carbohydrate interactions are required for high affinity binding between FcgammaRIII and antibodies lacking core fucose. Proc Natl Acad Sci U S A. 2011;108:12669-74.
    • (2011) Proc Natl Acad Sci U S A , vol.108 , pp. 12669-12674
    • Ferrara, C.1    Grau, S.2    Jager, C.3    Sondermann, P.4    Brunker, P.5    Waldhauer, I.6
  • 17
    • 84869431305 scopus 로고    scopus 로고
    • Intravenous immune globulin in autoimmune and inflammatory diseases
    • Gelfand EW. Intravenous immune globulin in autoimmune and inflammatory diseases. N Engl J Med. 2012;367:2015-25.
    • (2012) N Engl J Med , vol.367 , pp. 2015-2025
    • Gelfand, E.W.1
  • 18
    • 0036918050 scopus 로고    scopus 로고
    • Intravenous immunoglobulin mediates an increase in anti-platelet antibody clearance via the FcRn receptor
    • Hansen RJ, Balthasar JP. Intravenous immunoglobulin mediates an increase in anti-platelet antibody clearance via the FcRn receptor. Thromb Haemost. 2002;88:898-9. (Pubitemid 36018773)
    • (2002) Thrombosis and Haemostasis , vol.88 , Issue.6 , pp. 898-899
    • Hansen, R.J.1    Balthasar, J.P.2
  • 19
    • 84883545845 scopus 로고    scopus 로고
    • T cell-independent B cell activation induces immunosuppressive sialylated IgG antibodies
    • Hess C, Winkler A, Lorenz AK, Holecska V, Blanchard V, Eiglmeier S, et al. T cell-independent B cell activation induces immunosuppressive sialylated IgG antibodies. J Clin Invest. 2013;123:3788-96.
    • (2013) J Clin Invest , vol.123 , pp. 3788-3796
    • Hess, C.1    Winkler, A.2    Lorenz, A.K.3    Holecska, V.4    Blanchard, V.5    Eiglmeier, S.6
  • 21
    • 0026063099 scopus 로고
    • Immune thrombocytopenic purpura and intravenous immunoglobulin
    • Imbach P. Immune thrombocytopenic purpura and intravenous immunoglobulin. Cancer. 1991;68:1422-5.
    • (1991) Cancer , vol.68 , pp. 1422-1425
    • Imbach, P.1
  • 22
    • 0019522170 scopus 로고
    • High-dose intravenous gammaglobulin therapy of refractory, in particular idiopathic thrombocytopenia in childhood
    • Imbach P, Barandun S, Baumgartner C, Hirt A, Hofer F, Wagner HP. High-dose intravenous gammaglobulin therapy of refractory, in particular idiopathic thrombocytopenia in childhood. Helv Paediatr Acta. 1981;36:81-6. (Pubitemid 11137811)
    • (1981) Helvetica Paediatrica Acta , vol.36 , Issue.1 , pp. 81-86
    • Imbach, P.1    Barandun, S.2    Baumgartner, C.3
  • 23
    • 0019463420 scopus 로고
    • High-dose intravenous gammaglobulin for idiopathic thrombocytopenic purpura in childhood
    • Imbach P, Barandun S, d'Apuzzo V, Baumgartner C, Hirt A, Morell A, et al. High-dose intravenous gammaglobulin for idiopathic thrombocytopenic purpura in childhood. Lancet. 1981;1:1228-31.
    • (1981) Lancet , vol.1 , pp. 1228-1231
    • Imbach, P.1    Barandun, S.2    D'Apuzzo, V.3    Baumgartner, C.4    Hirt, A.5    Morell, A.6
  • 24
    • 77953141926 scopus 로고    scopus 로고
    • Superior in vivo efficacy of afucosylated trastuzumab in the treatment of HER2-amplified breast cancer
    • Junttila TT, Parsons K, Olsson C, Lu Y, Xin Y, Theriault J, et al. Superior in vivo efficacy of afucosylated trastuzumab in the treatment of HER2-amplified breast cancer. Cancer Res. 2010;70:4481-9.
    • (2010) Cancer Res , vol.70 , pp. 4481-4489
    • Junttila, T.T.1    Parsons, K.2    Olsson, C.3    Lu, Y.4    Xin, Y.5    Theriault, J.6
  • 25
    • 33746888249 scopus 로고    scopus 로고
    • Anti-inflammatory activity of immunoglobulin G resulting from Fc sialylation
    • DOI 10.1126/science.1129594
    • Kaneko Y, Nimmerjahn F, Ravetch JV. Anti-inflammatory activity of immunoglobulin G resulting from Fc sialylation. Science. 2006;313:670-3. (Pubitemid 44201145)
    • (2006) Science , vol.313 , Issue.5787 , pp. 670-673
    • Kaneko, Y.1    Nimmerjahn, F.2    Ravetch, J.V.3
  • 27
    • 84868642198 scopus 로고    scopus 로고
    • Anti-inflammatory activity of IgG1 mediated by Fc galactosylation and association of FcgammaRIIB and dectin-1
    • Karsten CM, Pandey MK, Figge J, Kilchenstein R, Taylor PR, Rosas M, et al. Anti-inflammatory activity of IgG1 mediated by Fc galactosylation and association of FcgammaRIIB and dectin-1. Nat Med. 2012;18:1401-6.
    • (2012) Nat Med , vol.18 , pp. 1401-1406
    • Karsten, C.M.1    Pandey, M.K.2    Figge, J.3    Kilchenstein, R.4    Taylor, P.R.5    Rosas, M.6
  • 28
    • 0037474543 scopus 로고    scopus 로고
    • Structural analysis of human IgG-Fc glycoforms reveals a correlation between glycosylation and structural integrity
    • DOI 10.1016/S0022-2836(02)01250-0
    • Krapp S, Mimura Y, Jefferis R, Huber R, Sondermann P. Structural analysis of human IgG-Fc glycoforms reveals a correlation between glycosylation and structural integrity. J Mol Biol. 2003;325:979-89. (Pubitemid 36263407)
    • (2003) Journal of Molecular Biology , vol.325 , Issue.5 , pp. 979-989
    • Krapp, S.1    Mimura, Y.2    Jefferis, R.3    Huber, R.4    Sondermann, P.5
  • 29
    • 0030470557 scopus 로고    scopus 로고
    • Multiple Interactions of IgG with Its Core Oligosaccharide Can Modulate Recognition by Complement and Human Fcgamma Receptor I and Influence the Synthesis of Its Oligosaccharide Chains
    • Lund J, Takahashi N, Pound JD, Goodall M, Jefferis R. Multiple interactions of IgG with its core oligosaccharide can modulate recognition by complement and human Fc gamma receptor I and influence the synthesis of its oligosaccharide chains. J Immunol. 1996;157:4963-9. (Pubitemid 126449574)
    • (1996) Journal of Immunology , vol.157 , Issue.11 , pp. 4963-4969
    • Lund, J.1    Takahashi, N.2    Pound, J.D.3    Goodall, M.4    Jefferis, R.5
  • 30
    • 80053578013 scopus 로고    scopus 로고
    • Impact of differential glycosylation on IgG activity
    • Lux A, Nimmerjahn F. Impact of differential glycosylation on IgG activity. Adv Exp Med Biol. 2011;780:113-24.
    • (2011) Adv Exp Med Biol , vol.780 , pp. 113-124
    • Lux, A.1    Nimmerjahn, F.2
  • 31
    • 0028962403 scopus 로고
    • Glycosylation changes of IgG associated with rheumatoid arthritis can activate complement via the mannose-binding protein
    • Malhotra R, Wormald MR, Rudd PM, Fischer PB, Dwek RA, Sim RB. Glycosylation changes of IgG associated with rheumatoid arthritis can activate complement via the mannose-binding protein. Nat Med. 1995;1:237-43.
    • (1995) Nat Med , vol.1 , pp. 237-243
    • Malhotra, R.1    Wormald, M.R.2    Rudd, P.M.3    Fischer, P.B.4    Dwek, R.A.5    Sim, R.B.6
  • 32
    • 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
    • DOI 10.1016/S0161-5890(00)00105-X, PII S016158900000105X
    • Mimura Y, Church S, Ghirlando R, Ashton PR, Dong S, Goodall M, et al. 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. 2000;37:697-706. (Pubitemid 32244118)
    • (2001) Molecular Immunology , vol.37 , Issue.12-13 , 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
  • 34
    • 0019934863 scopus 로고
    • Structural and numerical variations of the carbohydrate moiety of immunoglobulin G
    • Mizuochi T, Taniguchi T, Shimizu A, Kobata A. Structural and numerical variations of the carbohydrate moiety of immunoglobulin G. J Immunol. 1982;129:2016-20. (Pubitemid 12004362)
    • (1982) Journal of Immunology , vol.129 , Issue.5 , pp. 2016-2020
    • Mizuochi, T.1    Taniguchi, T.2    Shimizu, A.3    Kobata, A.4
  • 36
    • 42649089750 scopus 로고    scopus 로고
    • Anti-inflammatory actions of intravenous immunoglobulin
    • DOI 10.1146/annurev.immunol.26.021607.090232
    • Nimmerjahn F, Ravetch JV. Anti-inflammatory actions of intravenous immunoglobulin. Annu Rev Immunol. 2008;26:513-33. (Pubitemid 351600384)
    • (2008) Annual Review of Immunology , vol.26 , pp. 513-533
    • Nimmerjahn, F.1    Ravetch, J.V.2
  • 37
    • 12144289636 scopus 로고    scopus 로고
    • Defucosylated Chimeric Anti-CC Chemokine Receptor 4 IgG1 with Enhanced Antibody-Dependent Cellular Cytotoxicity Shows Potent Therapeutic Activity to T-Cell Leukemia and Lymphoma
    • DOI 10.1158/0008-5472.CAN-03-2068
    • Niwa R, Shoji-Hosaka E, Sakurada M, Shinkawa T, Uchida K, Nakamura K, et al. Defucosylated chimeric anti-CC chemokine receptor 4 IgG1 with enhanced antibody-dependent cellular cytotoxicity shows potent therapeutic activity to T-cell leukemia and lymphoma. Cancer Res. 2004;64:2127-33. (Pubitemid 38339463)
    • (2004) Cancer Research , vol.64 , Issue.6 , pp. 2127-2133
    • Niwa, R.1    Shoji-Hosaka, E.2    Sakurada, M.3    Shinkawa, T.4    Uehida, K.5    Nakamura, K.6    Matsushima, K.7    Ueda, R.8    Hanai, N.9    Shitara, K.10
  • 40
    • 0023912648 scopus 로고
    • Age-related galactosylation of the N-linked oligosaccharides of human serum IgG
    • Parekh R, Roitt I, Isenberg D, Dwek R, Rademacher T. Age-related galactosylation of the N-linked oligosaccharides of human serum IgG. J Exp Med. 1988;167:1731-6.
    • (1988) J Exp Med , vol.167 , pp. 1731-1736
    • Parekh, R.1    Roitt, I.2    Isenberg, D.3    Dwek, R.4    Rademacher, T.5
  • 41
    • 0022414766 scopus 로고
    • Association of rheumatoid arthritis and primary osteoarthritis with changes in the glycosylation pattern of total serum IgG
    • DOI 10.1038/316452a0
    • Parekh RB, Dwek RA, Sutton BJ, Fernandes DL, Leung A, Stanworth D, et al. Association of rheumatoid arthritis and primary osteoarthritis with changes in the glycosylation pattern of total serum IgG. Nature. 1985;316:452-7. (Pubitemid 16238456)
    • (1985) Nature , vol.316 , Issue.6027 , pp. 452-457
    • Parekh, R.B.1    Dwek, R.A.2    Sutton, B.J.3
  • 42
    • 79959850012 scopus 로고    scopus 로고
    • Passively administered pooled human immunoglobulins exert IL-10 dependent anti-inflammatory effects that protect against fatal HSV encephalitis
    • Ramakrishna C, Newo AN, Shen YW, Cantin E. Passively administered pooled human immunoglobulins exert IL-10 dependent anti-inflammatory effects that protect against fatal HSV encephalitis. PLoS Pathog. 2011;7:e1002071.
    • (2011) PLoS Pathog , vol.7
    • Ramakrishna, C.1    Newo, A.N.2    Shen, Y.W.3    Cantin, E.4
  • 43
    • 62649171202 scopus 로고    scopus 로고
    • Emerging methods for the production of homogeneous human glycoproteins
    • Rich JR, Withers SG. Emerging methods for the production of homogeneous human glycoproteins. Nat ChemBiol. 2009;5:206-15.
    • (2009) Nat ChemBiol , vol.5 , pp. 206-215
    • Rich, J.R.1    Withers, S.G.2
  • 44
    • 0035910392 scopus 로고    scopus 로고
    • Anti-inflammatory activity of IVIG mediated through the inhibitory Fc receptor
    • DOI 10.1126/science.291.5503.484
    • Samuelsson A, Towers TL, Ravetch JV. Anti-inflammatory activity of IVIG mediated through the inhibitory Fc receptor. Science. 2001;291:484-6. (Pubitemid 32097072)
    • (2001) Science , vol.291 , Issue.5503 , pp. 484-486
    • Samuelsson, A.1    Towers, T.L.2    Ravetch, J.V.3
  • 45
    • 33751253486 scopus 로고    scopus 로고
    • Higher levels of sialylated Fc glycans in immunoglobulin G molecules can adversely impact functionality
    • DOI 10.1016/j.molimm.2006.09.005, PII S0161589006005839
    • Scallon BJ, Tam SH, McCarthy SG, Cai AN, Raju TS. Higher levels of sialylated Fc glycans in immunoglobulin G molecules can adversely impact functionality. Mol Immunol. 2007;44:1524-34. (Pubitemid 44792756)
    • (2007) Molecular Immunology , vol.44 , Issue.7 , pp. 1524-1534
    • Scallon, B.J.1    Tam, S.H.2    McCarthy, S.G.3    Cai, A.N.4    Raju, T.S.5
  • 46
    • 84860257686 scopus 로고    scopus 로고
    • IVIg-mediated amelioration of ITP in mice is dependent on sialic acid and SIGNR1
    • Schwab I, Biburger M, Kronke G, Schett G, Nimmerjahn F. IVIg-mediated amelioration of ITP in mice is dependent on sialic acid and SIGNR1. Eur J Immunol. 2012;42:826-30.
    • (2012) Eur J Immunol , vol.42 , pp. 826-830
    • Schwab, I.1    Biburger, M.2    Kronke, G.3    Schett, G.4    Nimmerjahn, F.5
  • 47
    • 84899573297 scopus 로고    scopus 로고
    • Broad requirement for terminal sialic acid residues and FcgammaRIIB for the preventive and therapeutic activity of intravenous immunoglobulins in vivo
    • Schwab I, Mihai S, Seeling M, Kasperkiewicz M, Ludwig RJ, Nimmerjahn F. Broad requirement for terminal sialic acid residues and FcgammaRIIB for the preventive and therapeutic activity of intravenous immunoglobulins in vivo. Eur J Immunol. 2014.
    • (2014) Eur J Immunol
    • Schwab, I.1    Mihai, S.2    Seeling, M.3    Kasperkiewicz, M.4    Ludwig, R.J.5    Nimmerjahn, F.6
  • 48
    • 80053469048 scopus 로고    scopus 로고
    • Mechanisms and principles of N-linked protein glycosylation
    • Schwarz F, Aebi M. Mechanisms and principles of N-linked protein glycosylation. Curr Opin Struct Biol. 2011;21:576-82.
    • (2011) Curr Opin Struct Biol , vol.21 , pp. 576-582
    • Schwarz, F.1    Aebi, M.2
  • 52
    • 0036849054 scopus 로고    scopus 로고
    • Efficacy of IVIG affinity-purified anti-double-stranded DNA anti-idiotypic antibodies in the treatment of an experimental murine model of systemic lupus erythematosus
    • DOI 10.1093/intimm/dxf099
    • Shoenfeld Y, Rauova L, Gilburd B, Kvapil F, Goldberg I, Kopolovic J, et al. Efficacy of IVIG affinity-purified anti-double-stranded DNA anti-idiotypic antibodies in the treatment of an experimental murine model of systemic lupus erythematosus. Int Immunol. 2002;14:1303-11. (Pubitemid 35331427)
    • (2002) International Immunology , vol.14 , Issue.11 , pp. 1303-1311
    • Shoenfeld, Y.1    Rauova, L.2    Gilburd, B.3    Kvapil, F.4    Goldberg, I.5    Kopolovic, J.6    Rovensky, J.7    Blank, M.8
  • 53
    • 0042020026 scopus 로고    scopus 로고
    • Structure and function of natural-killer-cell receptors
    • Sun PD. Structure and function of natural-killer-cell receptors. Immunol Res. 2003;27:539-48.
    • (2003) Immunol Res , vol.27 , pp. 539-548
    • Sun, P.D.1
  • 54
    • 63849187507 scopus 로고    scopus 로고
    • Impaired inhibitory Fcgamma receptor IIB expression on B cells in chronic inflammatory demyelinating polyneuropathy
    • Tackenberg B, Jelcic I, Baerenwaldt A, Oertel WH, Sommer N, Nimmerjahn F, et al. Impaired inhibitory Fcgamma receptor IIB expression on B cells in chronic inflammatory demyelinating polyneuropathy. Proc Natl Acad Sci U S A. 2009;106:4788-92.
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 4788-4792
    • Tackenberg, B.1    Jelcic, I.2    Baerenwaldt, A.3    Oertel, W.H.4    Sommer, N.5    Nimmerjahn, F.6
  • 57
    • 0031028909 scopus 로고    scopus 로고
    • Variations in oligosaccharide-protein interactions in immunoglobulin G determine the site-specific glycosylation profiles and modulate the dynamic motion of the Fc oligosaccharides
    • DOI 10.1021/bi9621472
    • Wormald MR, Rudd PM, Harvey DJ, Chang SC, Scragg IG, Dwek RA. Variations in oligosaccharide-protein interactions in immunoglobulin G determine the site-specific glycosylation profiles and modulate the dynamic motion of the Fc oligosaccharides. Biochemistry. 1997;36:1370-80. (Pubitemid 27074961)
    • (1997) Biochemistry , vol.36 , Issue.6 , pp. 1370-1380
    • Wormald, M.R.1    Rudd, P.M.2    Harvey, D.J.3    Chang, S.-C.4    Scragg, I.G.5    Dwek, R.A.6
  • 58
    • 0030996004 scopus 로고    scopus 로고
    • Structural changes of immunoglobulin G oligosaccharides with age in healthy human serum
    • DOI 10.1023/A:1018582930906
    • Yamada E, Tsukamoto Y, Sasaki R, Yagyu K, Takahashi N. Structural changes of immunoglobulin G oligosaccharides with age in healthy human serum. Glycoconj J. 1997;14:401-5. (Pubitemid 27231681)
    • (1997) Glycoconjugate Journal , vol.14 , Issue.3 , pp. 401-405
    • Yamada, E.1    Tsukamoto, Y.2    Sasaki, R.3    Yagyu, K.4    Takahashi, N.5
  • 59
    • 84875749746 scopus 로고    scopus 로고
    • Dissecting the molecular mechanism of IVIg therapy: The interaction between serum IgG and DC-SIGN is independent of antibody glycoformor Fc domain
    • Yu X, Vasiljevic S, Mitchell DA, Crispin M, Scanlan CN. Dissecting the molecular mechanism of IVIg therapy: the interaction between serum IgG and DC-SIGN is independent of antibody glycoformor Fc domain. J Mol Biol. 2013;425:1253-8.
    • (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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.