4.5 Article

Delayed BCG immunization does not alter antibody responses to EPI vaccines in HIV-exposed and -unexposed South African infants

Journal

VACCINE
Volume 34, Issue 32, Pages 3702-3709

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2016.03.081

Keywords

BCG; Humoral immunity; Infants; HIV-exposed; South Africa

Funding

  1. Thrasher Research Fund [NR-0006]
  2. Elizabeth Glazer Pediatrics Aids Foundation International Leadership award [ZQ-00-8-520-0123-0-00]
  3. British Commonwealth Scholarship
  4. National Science Foundation

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Background: Bacille Calmette-Guerin (BCG) is routinely given at birth in tuberculosis-endemic settings due to its protective effect against disseminated tuberculosis in infants. BCG is however contraindicated in HIV-infected infants. We investigated whether delaying BCG vaccination to 14 weeks of age affected vaccine-induced antibody responses to Haemophilus influenzae type b (Hib)-conjugate, pertussis, tetanus and Hepatitis B (HBV) vaccines, in HIV-exposed uninfected (HEU) and -unexposed uninfected (HUU) infants. Methods: Infants were randomized to receive BCG at birth or at 14 weeks of age. Blood was taken at 14, 24, and 52 weeks of age and analyzed for Hib, pertussis, tetanus and HBV specific antibodies. Results: BCG was given either at birth (106 infants, 51 HEU) or at 14 weeks of age (74 infants, 50 HEU). The timing of BCG vaccination did not influence the antibody response to any antigen studied. However, in a non-randomized comparison, HEU infants had higher Hib antibody concentrations at weeks 14 and 24 (p=0.001 and <0.001, respectively) and pertussis at week 24 (p = 0.003). Conversely, HEU infants had lower antibody concentrations to HBV at 14 and 52 weeks (p = 0.032 and p = 0.031) with no differences in tetanus titres. Conclusions: HIV exposure, but not the timing of BCG vaccination, was associated with antibody concentrations to Hib, pertussis, HBV and tetanus primary immunization. (C) 2016 Elsevier Ltd. All rights reserved.

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