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Immunogenicity and reactogenicity of yellow fever vaccine in people with HIV

OBJECTIVE: To evaluate immunogenicity and reactogenicity of yellow fever (YF) vaccine in people with HIV (PWH) compared to HIV-uninfected controls. DESIGN: In this longitudinal interventional trial (NCT03132311), PWH with CD4(+) cell count ≥200 cells/μl and controls, aged 18–59, without a previous h...

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Detalles Bibliográficos
Autores principales: Motta, Edwiges, Camacho, Luiz Antonio B., Cunha, Marcelo, de Filippis, Ana Maria Bispo, Lima, Sheila M.B., Costa, Marcellus, Pedro, Luciana, Cardoso, Sandra W., Cortes, Fernanda Heloise, Giacoia-Gripp, Carmem B.W., Morata, Michelle, Nazer, Sandro, Moreira, Ronaldo Ismério, de Oliveira Souza, Marta Cristina, Mendes, Ygara S., de Souza Azevedo, Adriana, dos Santos Alvez, Nathalia, Grinsztejn, Beatriz, Coelho, Lara E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653289/
https://www.ncbi.nlm.nih.gov/pubmed/37650759
http://dx.doi.org/10.1097/QAD.0000000000003696
Descripción
Sumario:OBJECTIVE: To evaluate immunogenicity and reactogenicity of yellow fever (YF) vaccine in people with HIV (PWH) compared to HIV-uninfected controls. DESIGN: In this longitudinal interventional trial (NCT03132311), PWH with CD4(+) cell count ≥200 cells/μl and controls, aged 18–59, without a previous history of YF vaccination received a single standard dose of YF vaccine (17DD) and were followed at Days 5, 30 and Year 1. METHODS: YF-neutralization titers were measured at Days 0, 30 and Year 1 and geometric mean titers (GMT) were calculated. Adverse events (AE) and YF virus detection were measured at Days 5 and 30. Linear regression evaluated factors associated with YF-neutralization titers. RESULTS: Two hundred and eighteen PWH and 82 controls were included. At baseline, all PWH were using antiretroviral therapy; 92.6% had undetectable HIV viral load (VL) and median CD4(+) cell count was 630 cells/μl [interquartile range (IQR) 463–888]. YF vaccine was safe and there were no serious AEs. At Day 30, seroconversion was observed in 98.6% of PWH [95% confidence interval (CI): 95.6–99.6] and in 100% of controls (95% CI: 93.9–100); at Year 1, 94.0% of PWH (95% CI: 89.6–96.7) and 98.4% of controls (95% CI 90.3–99.9) were seropositive. PWH had lower GMTs than controls at Day 30 and Year 1. Baseline VL >1000 copies/ml, low CD4(+) cell count and low CD4(+)/CD8(+) ratio were associated with lower YF-neutralization titers. CONCLUSIONS: YF vaccine is safe in PWH with CD4(+) cell count ≥200 cells/μl. YF vaccine immunogenicity is impaired in PWH, particularly among those with high VL, low CD4(+) cell count and low CD4(+)/CD8(+) ratio at vaccination and YF-neutralization titers decays over time.