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Volumn 35, Issue 2, 2015, Pages 199-205

Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

(20)  Turley, A J a   Gathmann, B b   Bangs, C c   Bradbury, M d   Seneviratne, S e   Gonzalez Granado, L I f   Hackett, S g   Kutukculer, N h   Alachkar, H i   Hambleton, S j   Ritterbusch, H b   Kralickova, P k   Marodi, L l   Seidel, M G m   Dueckers, G n   Roesler, J o   Huissoon, A p   Baxendale, H q   Litzman, J r   Arkwright, P D d  


Author keywords

antibiotics; atypical hemolytic uremic syndrome; Complement; glomerulopathy; immunodeficiency; meningococcemia; Streptococcus pneumoniae; vaccination

Indexed keywords

ANTIBIOTIC AGENT; COMPLEMENT FACTOR; IMMUNOSUPPRESSIVE AGENT; MENINGOCOCCUS VACCINE; PNEUMOCOCCUS VACCINE; COMPLEMENT;

EID: 84925534410     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-015-0137-5     Document Type: Article
Times cited : (37)

References (40)
  • 1
    • 84907597606 scopus 로고    scopus 로고
    • Are complement deficiencies really rare? Overview on prevalence, clinical importance and modern diagnostic approach
    • COI: 1:CAS:528:DC%2BC2cXhtFGjs7vI, PID: 25037634
    • Grumach AS, Kirschfink M. Are complement deficiencies really rare? Overview on prevalence, clinical importance and modern diagnostic approach. Mol Immunol. 2014;61:110–7.
    • (2014) Mol Immunol , vol.61 , pp. 110-117
    • Grumach, A.S.1    Kirschfink, M.2
  • 2
    • 84901396869 scopus 로고    scopus 로고
    • Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry
    • COI: 1:CAS:528:DC%2BC2cXnvFSku7o%3D, PID: 24659230
    • Aghamohammadi A, Mohammadinejad P, Abolhassani H, Mirminachi B, Movahedi M, Gharagozlou M, et al. Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry. J Clin Immunol. 2014;34:478–90.
    • (2014) J Clin Immunol , vol.34 , pp. 478-490
    • Aghamohammadi, A.1    Mohammadinejad, P.2    Abolhassani, H.3    Mirminachi, B.4    Movahedi, M.5    Gharagozlou, M.6
  • 3
    • 0031886755 scopus 로고    scopus 로고
    • Primary immunodeficiency diseases in Latin America: first report from eight countries participating in the LAGID. Latin American Group for Primary Immunodeficiency Diseases
    • COI: 1:STN:280:DyaK1c7pt1entg%3D%3D, PID: 9533660
    • Zelazko M, Carneiro-Sampaio M, de Luigi Cornejo M, de Olarte Garcia D, Porras Madrigal O, Berron Perez R, et al. Primary immunodeficiency diseases in Latin America: first report from eight countries participating in the LAGID. Latin American Group for Primary Immunodeficiency Diseases. J Clin Immunol. 1998;18:161–6.
    • (1998) J Clin Immunol , vol.18 , pp. 161-166
    • Zelazko, M.1    Carneiro-Sampaio, M.2    de Luigi Cornejo, M.3    de Olarte Garcia, D.4    Porras Madrigal, O.5    Berron Perez, R.6
  • 4
    • 33748413638 scopus 로고    scopus 로고
    • Mannose-binding lectin in innate immunity: past, present and future
    • COI: 1:CAS:528:DC%2BD28Xht1ehsLjP, PID: 16948640
    • Dommett RM, Klein N, Turner MW. Mannose-binding lectin in innate immunity: past, present and future. Tissue Antigens. 2006;68:193–209.
    • (2006) Tissue Antigens , vol.68 , pp. 193-209
    • Dommett, R.M.1    Klein, N.2    Turner, M.W.3
  • 5
    • 33947137687 scopus 로고    scopus 로고
    • Secondary systemic lupus erythematosus: an analysis of 4 cases of uncontrolled hereditary angioedema
    • COI: 1:CAS:528:DC%2BD2sXjtValtL0%3D, PID: 17098477
    • Khan S, Tarzi MD, Doré PC, Sewell WA, Longhurst HJ. Secondary systemic lupus erythematosus: an analysis of 4 cases of uncontrolled hereditary angioedema. Clin Immunol. 2007;123:14–7.
    • (2007) Clin Immunol , vol.123 , pp. 14-17
    • Khan, S.1    Tarzi, M.D.2    Doré, P.C.3    Sewell, W.A.4    Longhurst, H.J.5
  • 6
    • 77955883153 scopus 로고    scopus 로고
    • Complement: a key system for immune surveillance and homeostasis
    • COI: 1:CAS:528:DC%2BC3cXhtVCmtbfO, PID: 20720586
    • Ricklin D, Hajishengallis G, Yang K, Lambris JD. Complement: a key system for immune surveillance and homeostasis. Nat Immunol. 2010;11:785–97.
    • (2010) Nat Immunol , vol.11 , pp. 785-797
    • Ricklin, D.1    Hajishengallis, G.2    Yang, K.3    Lambris, J.D.4
  • 7
    • 0014201786 scopus 로고
    • Inherited c’2 deficiency in man: lack of immunochemically detectable c’2 protein in serums from deficient individuals
    • COI: 1:STN:280:DC%2BC3cvktVWnsQ%3D%3D, PID: 17812292
    • Polley MJ. Inherited c’2 deficiency in man: lack of immunochemically detectable c’2 protein in serums from deficient individuals. Science. 1968;161:1149–51.
    • (1968) Science , vol.161 , pp. 1149-1151
    • Polley, M.J.1
  • 8
    • 0014942142 scopus 로고
    • Increased susceptibility to infection associated with abnormalities of complement-mediated functions and of the third component of complement (C3)
    • COI: 1:STN:280:DyaE3c%2FosVGhtA%3D%3D, PID: 4188976
    • Alper CA, Abramson N, Johnston RB, Jandl JH, Rosen FS. Increased susceptibility to infection associated with abnormalities of complement-mediated functions and of the third component of complement (C3). N Engl J Med. 1970;282:350–4.
    • (1970) N Engl J Med , vol.282 , pp. 350-354
    • Alper, C.A.1    Abramson, N.2    Johnston, R.B.3    Jandl, J.H.4    Rosen, F.S.5
  • 9
    • 0014752215 scopus 로고
    • Deficiency of the fourth component of complement in man
    • COI: 1:CAS:528:DyaE3cXpvVKitw%3D%3D, PID: 4190973
    • Torisu M, Sonozaki H, Inai S, Arata M. Deficiency of the fourth component of complement in man. J Immunol. 1970;104:728–37.
    • (1970) J Immunol , vol.104 , pp. 728-737
    • Torisu, M.1    Sonozaki, H.2    Inai, S.3    Arata, M.4
  • 10
    • 0014942136 scopus 로고
    • A familial deficiency of the phagocytosis-enhancing activity of serum relates to a dysfunction of the fifth component of complement (C5)
    • COI: 1:STN:280:DyaE3c%2FosVGhtQ%3D%3D, PID: 5411128
    • Miller ME, Nilsson UR. A familial deficiency of the phagocytosis-enhancing activity of serum relates to a dysfunction of the fifth component of complement (C5). N Engl J Med. 1970;282:354–8.
    • (1970) N Engl J Med , vol.282 , pp. 354-358
    • Miller, M.E.1    Nilsson, U.R.2
  • 11
    • 0015529237 scopus 로고
    • Lupus-erythematosus-like syndrome with a familial defect of complement
    • COI: 1:STN:280:DyaE387hslWlsg%3D%3D, PID: 4110615
    • Moncada B, Day NK, Good RA, Windhorst DB. Lupus-erythematosus-like syndrome with a familial defect of complement. N Engl J Med. 1972;286:689–93.
    • (1972) N Engl J Med , vol.286 , pp. 689-693
    • Moncada, B.1    Day, N.K.2    Good, R.A.3    Windhorst, D.B.4
  • 12
    • 0018319183 scopus 로고
    • Neisseria meningitidis and Neisseria gonorrhoeae bacteremia associated with C6, C7, or C8 deficiency
    • COI: 1:STN:280:DyaE1M7osFymug%3D%3D, PID: 109025
    • Petersen BH, Lee TJ, Snyderman R, Brooks GF. Neisseria meningitidis and Neisseria gonorrhoeae bacteremia associated with C6, C7, or C8 deficiency. Ann Intern Med. 1979;90:917–20.
    • (1979) Ann Intern Med , vol.90 , pp. 917-920
    • Petersen, B.H.1    Lee, T.J.2    Snyderman, R.3    Brooks, G.F.4
  • 13
    • 84891649590 scopus 로고    scopus 로고
    • Meningococcal disease and the complement system
    • PID: 24104403
    • Lewis LA, Ram S. Meningococcal disease and the complement system. Virulence. 2014;5:98–126.
    • (2014) Virulence , vol.5 , pp. 98-126
    • Lewis, L.A.1    Ram, S.2
  • 14
    • 84903987501 scopus 로고    scopus 로고
    • Invasive pneumococcal disease in children can reveal a primary immunodeficiency
    • COI: 1:CAS:528:DC%2BC2cXhtFensLnP, PID: 24759830
    • Gaschignard J, Levy C, Chrabieh M, Boisson B, Bost-Bru C, Dauger S, et al. Invasive pneumococcal disease in children can reveal a primary immunodeficiency. Clin Infect Dis. 2014;59:244–51.
    • (2014) Clin Infect Dis , vol.59 , pp. 244-251
    • Gaschignard, J.1    Levy, C.2    Chrabieh, M.3    Boisson, B.4    Bost-Bru, C.5    Dauger, S.6
  • 15
    • 84886250055 scopus 로고    scopus 로고
    • Atypical hemolytic uremic syndrome
    • COI: 1:CAS:528:DC%2BC3sXhs1yitbvJ, PID: 24161037
    • Kavanagh D, Goodship TH, Richards A. Atypical hemolytic uremic syndrome. Semin Nephrol. 2013;33:508–30.
    • (2013) Semin Nephrol , vol.33 , pp. 508-530
    • Kavanagh, D.1    Goodship, T.H.2    Richards, A.3
  • 16
    • 84949117415 scopus 로고    scopus 로고
    • Rodriguez E, Rallapalli PM, Osborne AJ, Perkins SJ. New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3. Biosci Rep 2014;34(5)
    • Rodriguez E, Rallapalli PM, Osborne AJ, Perkins SJ. New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3. Biosci Rep 2014;34(5).
  • 17
    • 84880799517 scopus 로고    scopus 로고
    • Complement therapy in atypical haemolytic uraemic syndrome (aHUS)
    • COI: 1:CAS:528:DC%2BC3sXhtVaitL7O, PID: 23810412
    • Wong EK, Goodship TH, Kavanagh D. Complement therapy in atypical haemolytic uraemic syndrome (aHUS). Mol Immunol. 2013;56:199–212.
    • (2013) Mol Immunol , vol.56 , pp. 199-212
    • Wong, E.K.1    Goodship, T.H.2    Kavanagh, D.3
  • 18
    • 84858668780 scopus 로고    scopus 로고
    • Membranoproliferative glomerulonephritis–a new look at an old entity
    • COI: 1:CAS:528:DC%2BC38XktlCqtLc%3D, PID: 22435371
    • Sethi S, Fervenza FC. Membranoproliferative glomerulonephritis–a new look at an old entity. N Engl J Med. 2012;366:1119–31.
    • (2012) N Engl J Med , vol.366 , pp. 1119-1131
    • Sethi, S.1    Fervenza, F.C.2
  • 19
    • 84864554927 scopus 로고    scopus 로고
    • Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies
    • COI: 1:CAS:528:DC%2BC38XhtFCku73K, PID: 22456601
    • Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, et al. Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Kidney Int. 2012;82:454–64.
    • (2012) Kidney Int , vol.82 , pp. 454-464
    • Servais, A.1    Noël, L.H.2    Roumenina, L.T.3    Le Quintrec, M.4    Ngo, S.5    Dragon-Durey, M.A.6
  • 20
    • 1942500177 scopus 로고    scopus 로고
    • Clinical and laboratory evaluation of complement deficiency
    • COI: 1:CAS:528:DC%2BD2cXjt1alsbo%3D, PID: 15100659
    • Wen L, Atkinson JP, Giclas PC. Clinical and laboratory evaluation of complement deficiency. J Allergy Clin Immunol. 2004;113:585–93.
    • (2004) J Allergy Clin Immunol , vol.113 , pp. 585-593
    • Wen, L.1    Atkinson, J.P.2    Giclas, P.C.3
  • 21
    • 79952469245 scopus 로고    scopus 로고
    • Autoimmunity and recurrent infections in partial complement C3 immunodeficiency
    • COI: 1:CAS:528:DC%2BC3cXkvFKksbY%3D
    • Rodriguez-Marco A, Bradbury M, Riley P, Arkwright PD. Autoimmunity and recurrent infections in partial complement C3 immunodeficiency. Rheumatology (Oxford). 2010;49:1017–9.
    • (2010) Rheumatology (Oxford) , vol.49 , pp. 1017-1019
    • Rodriguez-Marco, A.1    Bradbury, M.2    Riley, P.3    Arkwright, P.D.4
  • 22
    • 84891748872 scopus 로고    scopus 로고
    • Successful cure of C1q deficiency in human subjects treated with hematopoietic stem cell transplantation
    • COI: 1:CAS:528:DC%2BC3sXhsVKku7rF, PID: 24035158
    • Arkwright PD, Riley P, Hughes SM, Alachkar H, Wynn RF. Successful cure of C1q deficiency in human subjects treated with hematopoietic stem cell transplantation. J Allergy Clin Immunol. 2014;133:265–7.
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 265-267
    • Arkwright, P.D.1    Riley, P.2    Hughes, S.M.3    Alachkar, H.4    Wynn, R.F.5
  • 23
    • 1542318912 scopus 로고    scopus 로고
    • Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases
    • COI: 1:CAS:528:DC%2BD2cXhtlShu7w%3D, PID: 14978182
    • Dragon-Durey MA, Frémeaux-Bacchi V, Loirat C, Blouin J, Niaudet P, Deschenes G, et al. Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases. J Am Soc Nephrol. 2004;15:787–95.
    • (2004) J Am Soc Nephrol , vol.15 , pp. 787-795
    • Dragon-Durey, M.A.1    Frémeaux-Bacchi, V.2    Loirat, C.3    Blouin, J.4    Niaudet, P.5    Deschenes, G.6
  • 24
    • 75749153964 scopus 로고    scopus 로고
    • Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
    • COI: 1:CAS:528:DC%2BC3cXht1Kksrg%3D, PID: 20016463
    • Bienaime F, Dragon-Durey MA, Regnier CH, Nilsson SC, Kwan WH, Blouin J, et al. Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome. Kidney Int. 2010;77:339–49.
    • (2010) Kidney Int , vol.77 , pp. 339-349
    • Bienaime, F.1    Dragon-Durey, M.A.2    Regnier, C.H.3    Nilsson, S.C.4    Kwan, W.H.5    Blouin, J.6
  • 25
    • 84860711841 scopus 로고    scopus 로고
    • A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function
    • COI: 1:CAS:528:DC%2BC38XmvV2rsbk%3D, PID: 22246034
    • Roumenina LT, Frimat M, Miller EC, Provot F, Dragon-Durey MA, Bordereau P, et al. A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function. Blood. 2012;119:4182–91.
    • (2012) Blood , vol.119 , pp. 4182-4191
    • Roumenina, L.T.1    Frimat, M.2    Miller, E.C.3    Provot, F.4    Dragon-Durey, M.A.5    Bordereau, P.6
  • 26
    • 84862776696 scopus 로고    scopus 로고
    • Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations
    • COI: 1:CAS:528:DC%2BC38Xjt1eru7c%3D, PID: 22387014
    • Boteva L, Morris DL, Cortés-Hernández J, Martin J, Vyse TJ, Fernando MM. Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations. Am J Hum Genet. 2012;90:445–56.
    • (2012) Am J Hum Genet , vol.90 , pp. 445-456
    • Boteva, L.1    Morris, D.L.2    Cortés-Hernández, J.3    Martin, J.4    Vyse, T.J.5    Fernando, M.M.6
  • 27
    • 84879121370 scopus 로고    scopus 로고
    • Long-term safety and efficacy of sustained eculizumab treatment in patients with paroxysmal nocturnal haemoglobinuria
    • COI: 1:CAS:528:DC%2BC3sXps1Cks7s%3D, PID: 23617322
    • Hillmen P, Muus P, Röth A, Elebute MO, Risitano AM, Schrezenmeier H, et al. Long-term safety and efficacy of sustained eculizumab treatment in patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol. 2013;162:62–73.
    • (2013) Br J Haematol , vol.162 , pp. 62-73
    • Hillmen, P.1    Muus, P.2    Röth, A.3    Elebute, M.O.4    Risitano, A.M.5    Schrezenmeier, H.6
  • 28
    • 84878589219 scopus 로고    scopus 로고
    • Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
    • COI: 1:CAS:528:DC%2BC3sXpt1Oqu7k%3D, PID: 23738544
    • Legendre CM, Licht C, Muus P, Greenbaum LA, Babu S, Bedrosian C, et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med. 2013;368:2169–81.
    • (2013) N Engl J Med , vol.368 , pp. 2169-2181
    • Legendre, C.M.1    Licht, C.2    Muus, P.3    Greenbaum, L.A.4    Babu, S.5    Bedrosian, C.6
  • 29
    • 84858633062 scopus 로고    scopus 로고
    • Eculizumab and refractory membranoproliferative glomerulonephritis
    • COI: 1:CAS:528:DC%2BC38XktlCqtbc%3D, PID: 22435384
    • Radhakrishnan S, Lunn A, Kirschfink M, Thorner P, Hebert D, Langlois V, et al. Eculizumab and refractory membranoproliferative glomerulonephritis. N Engl J Med. 2012;366:1165–6.
    • (2012) N Engl J Med , vol.366 , pp. 1165-1166
    • Radhakrishnan, S.1    Lunn, A.2    Kirschfink, M.3    Thorner, P.4    Hebert, D.5    Langlois, V.6
  • 30
    • 0348078307 scopus 로고    scopus 로고
    • Long term effects of vaccination of patients deficient in a late complement component with a tetravalent meningococcal polysaccharide vaccine
    • COI: 1:CAS:528:DC%2BD3sXnvFSiuro%3D, PID: 14505927
    • Platonov AE, Vershinina IV, Kuijper EJ, Borrow R, Käyhty H. Long term effects of vaccination of patients deficient in a late complement component with a tetravalent meningococcal polysaccharide vaccine. Vaccine. 2003;21:4437–47.
    • (2003) Vaccine , vol.21 , pp. 4437-4447
    • Platonov, A.E.1    Vershinina, I.V.2    Kuijper, E.J.3    Borrow, R.4    Käyhty, H.5
  • 31
    • 12244257524 scopus 로고    scopus 로고
    • Opsonophagocytosis versus complement bactericidal killing as effectors following Neisseria meningitidis group C vaccination
    • COI: 1:STN:280:DC%2BD3s%2FnvVykug%3D%3D, PID: 12590334
    • Gomez-Lus ML, Giménez MJ, Vázquez JA, Aguilar L, Anta L, Berrón S, et al. Opsonophagocytosis versus complement bactericidal killing as effectors following Neisseria meningitidis group C vaccination. Infection. 2003;31:51–4.
    • (2003) Infection , vol.31 , pp. 51-54
    • Gomez-Lus, M.L.1    Giménez, M.J.2    Vázquez, J.A.3    Aguilar, L.4    Anta, L.5    Berrón, S.6
  • 32
    • 0037168558 scopus 로고    scopus 로고
    • The classical pathway is the dominant complement pathway required for innate immunity to Streptococcus pneumoniae infection in mice
    • Brown JS, Hussell T, Gilliland SM, Holden DW, Paton JC, Ehrenstein MR, et al. The classical pathway is the dominant complement pathway required for innate immunity to Streptococcus pneumoniae infection in mice. Proc Natl Acad Sci U S A. 2002;99:16–969.
    • (2002) Proc Natl Acad Sci U S A , vol.99 , pp. 16-969
    • Brown, J.S.1    Hussell, T.2    Gilliland, S.M.3    Holden, D.W.4    Paton, J.C.5    Ehrenstein, M.R.6
  • 33
    • 48849100792 scopus 로고    scopus 로고
    • Impaired opsonization with C3b and phagocytosis of Streptococcus pneumoniae in sera from subjects with defects in the classical complement pathway
    • COI: 1:CAS:528:DC%2BD1cXptF2hsrw%3D, PID: 18541650
    • Yuste J, Sen A, Truedsson L, Jönsson G, Tay LS, Hyams C, et al. Impaired opsonization with C3b and phagocytosis of Streptococcus pneumoniae in sera from subjects with defects in the classical complement pathway. Infect Immun. 2008;76:3761–70.
    • (2008) Infect Immun , vol.76 , pp. 3761-3770
    • Yuste, J.1    Sen, A.2    Truedsson, L.3    Jönsson, G.4    Tay, L.S.5    Hyams, C.6
  • 34
    • 84862267876 scopus 로고    scopus 로고
    • Complement factor I deficiency: a not so rare immune defect: characterization of new mutations and the first large gene deletion
    • PID: 22710145
    • Alba-Domínguez M, López-Lera A, Garrido S, Nozal P, González-Granado I, Melero J, et al. Complement factor I deficiency: a not so rare immune defect: characterization of new mutations and the first large gene deletion. Orphanet J Rare Dis. 2012;7:42.
    • (2012) Orphanet J Rare Dis , vol.7 , pp. 42
    • Alba-Domínguez, M.1    López-Lera, A.2    Garrido, S.3    Nozal, P.4    González-Granado, I.5    Melero, J.6
  • 35
    • 84934437847 scopus 로고    scopus 로고
    • Paroxysmal nocturnal hemoglobinuria and the complement system: recent insights and novel anticomplement strategies
    • COI: 1:CAS:528:DC%2BC3sXhtVWgs77N, PID: 23402025
    • Risitano AM. Paroxysmal nocturnal hemoglobinuria and the complement system: recent insights and novel anticomplement strategies. Adv Exp Med Biol. 2013;735:155–72.
    • (2013) Adv Exp Med Biol , vol.735 , pp. 155-172
    • Risitano, A.M.1
  • 36
    • 84878214672 scopus 로고    scopus 로고
    • Immunology of age-related macular degeneration
    • COI: 1:CAS:528:DC%2BC3sXotFSmurg%3D, PID: 23702979
    • Ambati J, Atkinson JP, Gelfand BD. Immunology of age-related macular degeneration. Nat Rev Immunol. 2013;13:438–51.
    • (2013) Nat Rev Immunol , vol.13 , pp. 438-451
    • Ambati, J.1    Atkinson, J.P.2    Gelfand, B.D.3
  • 37
    • 85018154948 scopus 로고    scopus 로고
    • Prevention and control of meningococcal disease. Recommendations of the advisory committee on immunization practices
    • Centers for Disease Control and Prevention. Prevention and control of meningococcal disease. Recommendations of the advisory committee on immunization practices. Morbidy and Mortality weekly report. 2013; 62:2.
    • (2013) Morbidy and Mortality weekly report , vol.62 , pp. 2
  • 38
    • 84908553399 scopus 로고    scopus 로고
    • Preventing secondary cases of invasive meningococcal capsular group B (MenB) disease using a recently-licensed, multi-component, protein-based vaccine (Bexsero(®))
    • PID: 25043395
    • Ladhani SN, Cordery R, Mandal S, Christensen H, Campbell H, Borrow R, et al. Preventing secondary cases of invasive meningococcal capsular group B (MenB) disease using a recently-licensed, multi-component, protein-based vaccine (Bexsero(®)). J Infect. 2014;69:470–80.
    • (2014) J Infect , vol.69 , pp. 470-480
    • Ladhani, S.N.1    Cordery, R.2    Mandal, S.3    Christensen, H.4    Campbell, H.5    Borrow, R.6
  • 39
    • 84886997343 scopus 로고    scopus 로고
    • Antibiotic prophylaxis in primary immune deficiency disorders
    • PID: 24565703
    • Kuruvilla M, de la Morena MT. Antibiotic prophylaxis in primary immune deficiency disorders. J Allergy Clin Immunol Pract. 2013;1:573–82.
    • (2013) J Allergy Clin Immunol Pract , vol.1 , pp. 573-582
    • Kuruvilla, M.1    de la Morena, M.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.