Long-Term Serological Response to 13-Valent Pneumococcal Conjugate Vaccine Versus 23-Valent Polysaccharide Vaccine in HIV-Infected Adults.

HIV PCV13 PPV23 Pneumococcal vaccination Serologic response Streptococcus pneumoniae

Journal

Infectious diseases and therapy
ISSN: 2193-8229
Titre abrégé: Infect Dis Ther
Pays: New Zealand
ID NLM: 101634499

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 10 06 2019
pubmed: 1 8 2019
medline: 1 8 2019
entrez: 1 8 2019
Statut: ppublish

Résumé

Long-term comparative immunologic response to 13-valent pneumococcal conjugate vaccine (PCV13) versus 23-valent polysaccharide vaccine (PPV23) among HIV-infected adults has not yet been investigated. In this prospective pilot study, we quantified in HIV-positive adults serotype-specific IgG concentrations of the 12 pneumococcal serotypes shared by both vaccines 5 years after vaccination with two doses of PCV13 8 weeks apart (group 1) or one dose of PPV23 (group 2) and compared them with those assessed prior to vaccination (BL) and after 1 year (T1). Comparison of immunogenicity was based on geometric mean concentration (GMC), proportion of individuals with ≥ twofold increase from BL in specific antibody concentration against ≥ 2 serotypes and percentage of individuals with serotype-specific IgG ≥ 0.35 μg/ml, ≥ 1 μg/ml and ≥ individual serotype-specific correlates of protection. We included 91 subjects (median CD4 In this study with HIV-positive adults with a favorable viro-immunologic profile, both vaccines were shown to achieve a long-term durable serologic response. We found minor differences in immunogenicity between the two vaccines, which favored PCV13 over PPV23 5 years after immunization. ClinicalTrials.gov identifier, NCT02123433.

Identifiants

pubmed: 31364010
doi: 10.1007/s40121-019-0256-z
pii: 10.1007/s40121-019-0256-z
pmc: PMC6702530
doi:

Banques de données

ClinicalTrials.gov
['NCT02123433']

Types de publication

Journal Article

Langues

eng

Pagination

453-462

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Auteurs

Simone Belmonti (S)

Istituto di Clinica Malattie Infettive, Università Cattolica del Sacro Cuore, Rome, Italy.

Barbara Rossetti (B)

Hospital Department of Specialized and Internal Medicine, University Division of Infectious Diseases, Viale Bracci 16, 53100, Siena, Italy.

Sara Modica (S)

Department of Medical Biotechnologies, University of Siena, Viale Bracci 16, 53100, Siena, Italy.

Lorenzo Paglicci (L)

Department of Medical Biotechnologies, University of Siena, Viale Bracci 16, 53100, Siena, Italy.

Alberto Borghetti (A)

Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Malattie Infettive, Rome, Italy.

Arturo Ciccullo (A)

Istituto di Clinica Malattie Infettive, Università Cattolica del Sacro Cuore, Rome, Italy.

Chiara Picarelli (C)

Istituto di Clinica Malattie Infettive, Università Cattolica del Sacro Cuore, Rome, Italy.

Roberto Cauda (R)

Istituto di Clinica Malattie Infettive, Università Cattolica del Sacro Cuore, Rome, Italy.
Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Malattie Infettive, Rome, Italy.

Andrea De Luca (A)

Hospital Department of Specialized and Internal Medicine, University Division of Infectious Diseases, Viale Bracci 16, 53100, Siena, Italy.
Department of Medical Biotechnologies, University of Siena, Viale Bracci 16, 53100, Siena, Italy.

Francesca Montagnani (F)

Hospital Department of Specialized and Internal Medicine, University Division of Infectious Diseases, Viale Bracci 16, 53100, Siena, Italy.
Department of Medical Biotechnologies, University of Siena, Viale Bracci 16, 53100, Siena, Italy.

Francesca Lombardi (F)

Istituto di Clinica Malattie Infettive, Università Cattolica del Sacro Cuore, Rome, Italy. francesca.lombardi@gmail.com.

Classifications MeSH