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Immune response to a Tdap booster in vertically HIV-infected adolescents
- Spina, Fernanda Garcia, Gouvea, Aída, Succi, Regina Célia de Menezes, Calanca, Flavia, Weckx, Lily Yin, Terreri, Maria Teresa, Takano, Maria Aparecida Sakauchi, de Moraes-Pinto, Maria Isabel
- Vaccine 2018 v.36 no.37 pp. 5609-5616
- Bordetella pertussis, CD4-positive T-lymphocytes, HIV infections, adolescents, antibodies, antigens, blood sampling, cell-mediated immunity, enzyme-linked immunosorbent assay, flow cytometry, geometry, humoral immunity, immune response, injection site, interferon-gamma, interleukin-10, interleukin-13, interleukin-4, interleukin-5, lymphocyte count, pain, pertussis toxin, tetanus, vaccines
- Pertussis cases have increased worldwide and knowledge on immune response and cytokine profile after Tdap vaccine in immunodeficient adolescents is scarce.To evaluate the immune response after Tdap in HIV-infected (HIV) and in healthy adolescents (CONTROL).Thirty HIV adolescents with CD4 cell counts >200 and 30 CONTROLs were immunized with Tdap, after a prior whole-cell DTP vaccine primary scheme. Blood samples were collected immediately before and after vaccine. Lymphocyte immunophenotyping was performed by flow cytometry; tetanus, diphtheria and pertussis toxin antibodies were assessed by ELISA; whole blood was stimulated with tetanus toxoid and Bordetella pertussis and supernatants were assessed for cytokines by xMAP.Mean age of HIV and CONTROL groups were 17.9 e 17.1 years, respectively. Pain at injection site was more intense in CONTROL group. HIV group had similar increase in tetanus antibodies at 28 days (geometric mean concentration, GMC, 15.6; 95% CI, 7.52–32.4) than CONTROL group (GMC, 23.1; 95% CI, 15.0–35.5), but lower diphtheria antibodies at 28 days (GMC, 2.3; 95% CI, 0.88–6.19) than CONTROL group (GMC, 16.4; 95% CI, 10.3–26.2); for pertussis, the percentage of individuals who seroconverted was lower in HIV than CONTROL group (HIV, 62.1% versus CONTROL, 100%; p = .002). Both groups built a cellular immune response to tetanus, with a Th2 (IL-4, IL-5 and IL-13) and Th1 (IFN-γ) response, with lower cytokine levels in HIV than in CONTROL group. Especially for pertussis, cellular and humoral responses were less intense in HIV adolescents, with a lower Th1 and Th17 profile and higher IL-10 levels. HIV-infected adolescents on viral suppression showed an enhanced immune response to all the three vaccine antigens, although still at lower levels if compared to CONTROL group.Both groups tolerated well and built an immune response after Tdap. However, HIV-infected adolescents would probably benefit from more frequent booster doses.