Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV

Objectives: To evaluate safety and immunogenicity of V114 [15-valent pneumococcal conjugate vaccine (PCV) containing serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 22F, 23F, and 33F], followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 8 weeks later, in adults living with HI...

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Main Author: Mohapi L.
Other Authors: Mahidol University
Format: Article
Published: 2023
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/85018
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spelling th-mahidol.850182023-06-19T00:24:18Z Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV Mohapi L. Mahidol University Immunology and Microbiology Objectives: To evaluate safety and immunogenicity of V114 [15-valent pneumococcal conjugate vaccine (PCV) containing serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 22F, 23F, and 33F], followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 8 weeks later, in adults living with HIV. Design: In this phase 3 study (V114-018; NCT03480802), pneumococcal vaccinenaive adults with HIV (CD4 cell count _50 cells/ml, plasma HIV RNA <50 000 copies/ ml, receiving antiretroviral therapy) were randomized 1 : 1 to receive one dose of V114 or licensed 13-valent PCV (PCV13) on day 1; participants received PPSV23 at week 8. Methods: Adverse events and serotype-specific opsonophagocytic activity (OPA) and immunoglobulin G (IgG) antibodies were evaluated after each vaccination. Results: Of 302 participants enrolled, 292 (96.7%) completed the study. Proportions of participants experiencing at least one adverse event were 73.0 and 62.7% in the V114 and PCV13 groups following PCV and 60.7 and 71.6%following PPSV23. Most solicited adverse events were of mild or moderate severity and short duration. OPA geometric mean titers (GMTs) and IgG geometric mean concentrations (GMCs) were generally comparable between groups for shared serotypes at day 30 and maintained at week 12. OPA and IgGresponses for additional serotypes in V114 (22F, 33F) were higher following V114 than PCV13 at day 30 but comparable at week 12, 30 days post-PPSV23. Conclusion: In pneumococcal vaccine-naive adults living with HIV, V114 was well tolerated and induced immune responses for all 15 pneumococcal serotypes. V114 can be followed by PPSV23 8 weeks later to broaden serotype coverage. 2023-06-18T17:24:18Z 2023-06-18T17:24:18Z 2022-03-01 Article AIDS Vol.36 No.3 (2022) , 373-382 10.1097/QAD.0000000000003126 14735571 02699370 34750291 2-s2.0-85123901465 https://repository.li.mahidol.ac.th/handle/123456789/85018 SCOPUS
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Immunology and Microbiology
spellingShingle Immunology and Microbiology
Mohapi L.
Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV
description Objectives: To evaluate safety and immunogenicity of V114 [15-valent pneumococcal conjugate vaccine (PCV) containing serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 22F, 23F, and 33F], followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 8 weeks later, in adults living with HIV. Design: In this phase 3 study (V114-018; NCT03480802), pneumococcal vaccinenaive adults with HIV (CD4 cell count _50 cells/ml, plasma HIV RNA <50 000 copies/ ml, receiving antiretroviral therapy) were randomized 1 : 1 to receive one dose of V114 or licensed 13-valent PCV (PCV13) on day 1; participants received PPSV23 at week 8. Methods: Adverse events and serotype-specific opsonophagocytic activity (OPA) and immunoglobulin G (IgG) antibodies were evaluated after each vaccination. Results: Of 302 participants enrolled, 292 (96.7%) completed the study. Proportions of participants experiencing at least one adverse event were 73.0 and 62.7% in the V114 and PCV13 groups following PCV and 60.7 and 71.6%following PPSV23. Most solicited adverse events were of mild or moderate severity and short duration. OPA geometric mean titers (GMTs) and IgG geometric mean concentrations (GMCs) were generally comparable between groups for shared serotypes at day 30 and maintained at week 12. OPA and IgGresponses for additional serotypes in V114 (22F, 33F) were higher following V114 than PCV13 at day 30 but comparable at week 12, 30 days post-PPSV23. Conclusion: In pneumococcal vaccine-naive adults living with HIV, V114 was well tolerated and induced immune responses for all 15 pneumococcal serotypes. V114 can be followed by PPSV23 8 weeks later to broaden serotype coverage.
author2 Mahidol University
author_facet Mahidol University
Mohapi L.
format Article
author Mohapi L.
author_sort Mohapi L.
title Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV
title_short Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV
title_full Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV
title_fullStr Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV
title_full_unstemmed Safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, in adults living with HIV
title_sort safety and immunogenicity of v114, a 15-valent pneumococcal conjugate vaccine, in adults living with hiv
publishDate 2023
url https://repository.li.mahidol.ac.th/handle/123456789/85018
_version_ 1781414197449457664