Geraldo Duarte1, Petronella Muresan2, Shawn Ward2, Lauren Laimon3, Stephen I Pelton4, Jennifer Canniff5, Amanda Golner6, Frederic Bone6, Lassallete Newton3, Terence Fenton2, Conrado M Coutinho1, Esau C João7, Breno R Santos8, Jose H Pilotto9, Ricardo H Oliveira10, Jorge A Pinto11, Elizabeth S Machado10, Regis Kreitchman12, Nahida Chakhtoura13, Marisa M Mussi-Pinhata14, Adriana Weinberg5. 1. Department of Obstetrics and Gynecology, Ribeirão Preto Medical School, University of São Paulo, Ribeirao Preto, Brazil. 2. Frontier Science Foundation, Brookline, Massachusetts, USA. 3. Westat, Rockville, Maryland, USA. 4. Boston University School of Medicine, Boston, Massachusetts, USA. 5. Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA. 6. Frontier Science Foundation, Buffalo, New York, USA. 7. Hospital dos Servidores Estaduais, Rio de Janeiro, Brazil. 8. Hospital Nossa Senhora da Conceicao, Porto Alegre, Brazil. 9. Hospital Geral de Nova Iguaçu, Rio de Janeiro, Brazil. 10. Instituto de Puericultura e Pediatra Matagão Gesteira, Rio de Janeiro, Brazil. 11. School of Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil. 12. Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil. 13. Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA. 14. Department of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirao Preto, Brazil.
Abstract
BACKGROUND: Pneumococcal vaccination is recommended in people with HIV, prioritizing PCV. We compared the immunogenicity of PCV-10 and PPV-23 administered antepartum or postpartum. METHODS: This double-blind study randomized 346 pregnant women with HIV on antiretrovirals to PCV-10, PPV-23, or placebo at 14-34 weeks gestational age. Women who received placebo antepartum were randomized at 24 weeks postpartum to PCV-10 or PPV-23. Antibodies against 7 serotypes common to both vaccines and 1 serotype only in PPV-23 were measured by ELISA/chemiluminescence; B- and T-cell responses to serotype 1 by FLUOROSPOT; and plasma cytokines/chemokines by chemiluminescence. RESULTS: Antibody responses were higher after postpartum versus antepartum vaccination. PCV-10 generated lower antibody levels than PPV-23 against 4 and higher against 1 of 7 common serotypes. Additional factors associated with high postvaccination antibody concentrations were high prevaccination antibody concentrations and CD4+ cells; low CD8+ cells and plasma HIV RNA; and several plasma cytokines/chemokines. Serotype 1 B- and T-cell memory did not increase after vaccination. CONCLUSIONS: Antepartum immunization generated suboptimal antibody responses, suggesting that postpartum booster doses may be beneficial and warrant further studies. Considering that PCV-10 and PPV-23 had similar immunogenicity, but PPV-23 covered more serotypes, use of PPV-23 may be prioritized in women with HIV on antiretroviral therapy. CLINICAL TRAILS REGISTRATION: NCT02717494.
BACKGROUND: Pneumococcal vaccination is recommended in people with HIV, prioritizing PCV. We compared the immunogenicity of PCV-10 and PPV-23 administered antepartum or postpartum. METHODS: This double-blind study randomized 346 pregnant women with HIV on antiretrovirals to PCV-10, PPV-23, or placebo at 14-34 weeks gestational age. Women who received placebo antepartum were randomized at 24 weeks postpartum to PCV-10 or PPV-23. Antibodies against 7 serotypes common to both vaccines and 1 serotype only in PPV-23 were measured by ELISA/chemiluminescence; B- and T-cell responses to serotype 1 by FLUOROSPOT; and plasma cytokines/chemokines by chemiluminescence. RESULTS: Antibody responses were higher after postpartum versus antepartum vaccination. PCV-10 generated lower antibody levels than PPV-23 against 4 and higher against 1 of 7 common serotypes. Additional factors associated with high postvaccination antibody concentrations were high prevaccination antibody concentrations and CD4+ cells; low CD8+ cells and plasma HIV RNA; and several plasma cytokines/chemokines. Serotype 1 B- and T-cell memory did not increase after vaccination. CONCLUSIONS: Antepartum immunization generated suboptimal antibody responses, suggesting that postpartum booster doses may be beneficial and warrant further studies. Considering that PCV-10 and PPV-23 had similar immunogenicity, but PPV-23 covered more serotypes, use of PPV-23 may be prioritized in women with HIV on antiretroviral therapy. CLINICAL TRAILS REGISTRATION: NCT02717494.
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