Immunogenicity and Reactogenicity of 2009 Influenza A (H1N1) Inactivated Monovalent Non-Adjuvanted Vaccine in Elderly and Immunocompromised Patients


Autoria(s): Miraglia, João L.; Abdala, Edson; Hoff, Paulo M.; Luiz, Andre M.; Oliveira, Danise Senna; Saad, Carla Gonçalves Schahin; Laurindo, Ieda Maria Magalhães; Viso, Ana Teresa Rodriguez; Tayra, Angela; Pierrotti, Lígia Camera; Azevedo, Luiz S.; Campos, Lúcia Maria Mattei de Arruda; Aikawa, Nádia Emi; Timenetsky, Maria do Carmo Sampaio Tavares; Luna, Expedito José de Albuquerque; Cardoso, Maria Regina Alves; Guedes, José da Silva; Raw, Isaias; Jorge, Kalil; Precioso, Alexander Roberto; Hoff, Paulo M.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

10/03/2014

10/03/2014

10/03/2014

Resumo

Background Immunosuppressed individuals present serious morbidity and mortality from influenza, therefore it is important to understand the safety and immunogenicity of influenza vaccination among them. Methods This multicenter cohort study evaluated the immunogenicity and reactogenicity of an inactivated, monovalent, non-adjuvanted pandemic (H1N1) 2009 vaccine among the elderly, HIV-infected, rheumatoid arthritis (RA), cancer, kidney transplant, and juvenile idiopathic arthritis (JIA) patients. Participants were included during routine clinical visits, and vaccinated according to conventional influenza vaccination schedules. Antibody response was measured by the hemagglutination-inhibition assay, before and 21 days after vaccination. Results 319 patients with cancer, 260 with RA, 256 HIV-infected, 149 elderly individuals, 85 kidney transplant recipients, and 83 with JIA were included. The proportions of seroprotection, seroconversion, and the geometric mean titer ratios postvaccination were, respectively: 37.6%, 31.8%, and 3.2 among kidney transplant recipients, 61.5%, 53.1%, and 7.5 among RA patients, 63.1%, 55.7%, and 5.7 among the elderly, 59.0%, 54.7%, and 5.9 among HIV-infected patients, 52.4%, 49.2%, and 5.3 among cancer patients, 85.5%, 78.3%, and 16.5 among JIA patients. The vaccine was well tolerated, with no reported severe adverse events. Conclusions The vaccine was safe among all groups, with an acceptable immunogenicity among the elderly and JIA patients, however new vaccination strategies should be explored to improve the immune response of immunocompromised adult patients. (ClinicalTrials.gov, NCT01218685)

Fundação Butantan funded the study, and employed several of the authors. The funder had a role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Identificador

Plos One, v. 6, n. 11, p. 27214 (7p.), 2011.

http://www.producao.usp.br/handle/BDPI/44093

10.1371/journal.pone.0027214

http://www.plosone.org/article/fetchObject.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0027214&representation=PDF

Idioma(s)

eng

Publicador

San Francisco

Relação

PLOS ONE

Direitos

openAccess

http://creativecommons.org/licenses/by-nc-nd/3.0/br/

Plos

Palavras-Chave #H1N1 #Vaccine #Immunocompromised Patients
Tipo

article

original article

publishedVersion