Quantitative and qualitative antibody response to pneumococcal conjugate vaccine among African human immunodeficiency virus-infected and uninfected children

被引:69
作者
Madhi, SA [1 ]
Kuwanda, L
Cutland, C
Holm, A
Käyhty, H
Klugman, KP
机构
[1] Univ Witwatersrand, Natl Inst Communicable Dis, MRC, Johannesburg, South Africa
[2] Univ Witwatersrand, Resp & Meningeal Pathogens Res Unit, Wits Hlth Consortium, Johannesburg, South Africa
[3] Univ Witwatersrand, Paediat Infect Dis Res Unit, Wits Hlth Consortium, Johannesburg, South Africa
[4] Natl Publ Hlth Inst, Helsinki, Finland
[5] Emory Univ, Sch Med, Dept Int Hlth, Rollins Sch Publ Hlth & Infect Dis, Atlanta, GA 30322 USA
关键词
pneumococcus; conjugate vaccine; hurnan immunodeficiency virus; pneumonia;
D O I
10.1097/01.inf.0000160942.84169.14
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To determine the quantitative and qualitative antibody responses to a pneumococcal conjugate vaccine (PnCV) in human immunodeficiency virus (HIV)-exposed infected and uninfected children. Methods: Children were randomized to receive either a PnCV or placebo at 6, 10 and 14 weeks of age. PnCV serotype-specific antibody concentrations were measured by a standard enzyme immunoassay (EIA) and a 22F modified EIA (22F EIA) on single serum samples drawn at 21-42 days post-dose 3. Functional activities of the serotype-specific antibody to serotypes 613, 19F and 23F were measured with an opsonophagocytic assay (OPA). Results: The geometric mean antibody concentrations (GMC) were similar in HIV-infected and HIV-uninfected PnCV recipients for 7 of the 9 vaccine serotypes. In placebo recipients, the GMCs were significantly higher in HIV-infected than in uninfected children for 7 of the serotypes. In HIV-infected PnCV recipients, the GMCs were lower for 5 of the serotypes in children with severe acquired immunodeficiency syndrome than in children who were asymptomatic or mildly symptomatic with acquired immunodeficiency syndrome. HIV-infected PnCV recipients were less likely to have measurable functional antibody (OPA titer >= 1/8) to all 3 studied serotypes (6B, 19F and 23F) than in HIV-uninfected children. HIV-infected children required a higher concentration of anticapsular antibody to achieve 50% of the maximum uptake of labeled Streptococcus pneumoniae in the OPA assay than HIV-uninfected children for 2 of the 3 serotypes, although this was significant only for serotype 6B (P = 0.0005). Conclusion: HIV-infected children have similar quantitative antibody responses but poorer qualitative antibody responses to the PnCV.
引用
收藏
页码:410 / 416
页数:7
相关论文
共 24 条
[1]   DEFECTIVE HUMORAL IMMUNITY IN PEDIATRIC ACQUIRED IMMUNE-DEFICIENCY SYNDROME [J].
BERNSTEIN, LJ ;
OCHS, HD ;
WEDGWOOD, RJ ;
RUBINSTEIN, A .
JOURNAL OF PEDIATRICS, 1985, 107 (03) :352-357
[2]   Efficacy, safety and immunogenicity of heptavalent pneumococcal conjugate vaccine in children [J].
Black, S ;
Shinefield, H ;
Fireman, B ;
Lewis, E ;
Ray, P ;
Hansen, JR ;
Elvin, L ;
Ensor, KM ;
Hackell, J ;
Siber, G ;
Malinoski, F ;
Madore, D ;
Chang, I ;
Kohberger, R ;
Watson, W ;
Austrian, R ;
Edwards, K .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (03) :187-195
[3]   Pneumococcal type 22F polysaccharide absorption improves the specificity of a pneumococcal-polysaccharide enzyme-linked immunosorbent assay [J].
Concepcion, NF ;
Frasch, CE .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (02) :266-272
[4]   IMPAIRED NEUTROPHIL FUNCTION IN PATIENTS WITH AIDS OR AIDS-RELATED COMPLEX - A COMPREHENSIVE EVALUATION [J].
ELLIS, M ;
GUPTA, S ;
GALANT, S ;
HAKIM, S ;
VANDEVEN, C ;
TOY, C ;
CAIRO, MS .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (06) :1268-1276
[5]   Efficacy of a pneumococcal conjugate vaccine against acute otitis media [J].
Eskola, J ;
Kilpi, T ;
Palmu, A ;
Jokinen, J ;
Haapakoski, J ;
Herva, E ;
Takala, A ;
Käyhty, H ;
Karma, P ;
Kohberger, R ;
Siber, G ;
Mäkela, PH ;
Lockhart, S ;
Ecrola, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (06) :403-409
[6]   Specificity of the antibody response to the pneumococcal polysaccharide and conjugate vaccines in human immunodeficiency virus-infected adults [J].
Feikin, DR ;
Elie, CM ;
Goetz, MB ;
Lennox, JL ;
Carlone, GM ;
Romero-Steiner, S ;
Holder, PF ;
O'Brien, WA ;
Whitney, CG ;
Butler, JC ;
Breiman, RF .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2004, 11 (01) :137-141
[7]   Killing of Streptococcus pneumoniae by capsular polysaccharide-specific polymeric IgA, complement, and phagocytes [J].
Janoff, EN ;
Fasching, C ;
Orenstein, JM ;
Rubins, JB ;
Opstad, NL ;
Dalmasso, AP .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (08) :1139-1147
[8]   Protective efficacy of a second pneumococcal conjugate vaccine against pneumococcal acute otitis media in infants and children:: Randomized, controlled trial of a 7-valent pneumococcal polysaccharide-meningococcal outer membrane protein complex conjugate vaccine in 1666 children [J].
Kilpi, T ;
Åhman, H ;
Jokinen, J ;
Lankinen, KS ;
Palmu, A ;
Savolainen, H ;
Grönholm, M ;
Leinonen, M ;
Hovi, T ;
Eskola, J ;
Käyhty, H ;
Bohidar, N ;
Sadoff, JC ;
Mäkelä, PH .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (09) :1155-1164
[9]   Safety and immunogenicity of three doses of a five-valent pneumococcal conjugate vaccine in children younger than two years with and without human immunodeficiency virus infection [J].
King, JC ;
Vink, PE ;
Farley, JJ ;
Smilie, M ;
Parks, M ;
Lichenstein, R .
PEDIATRICS, 1997, 99 (04) :575-580
[10]   Antibody titers eight months after three doses of a five-valent pneumococcal conjugate vaccine in HIV and non-HIV-infected children less than two years of age [J].
King, JC ;
Vink, PE ;
Chang, I ;
Kimura, A ;
Parks, M ;
Smilie, M ;
Lichenstein, R ;
Farley, JJ .
VACCINE, 1998, 16 (04) :361-365