Given the resurgence of
pertussis despite high rates of vaccination with the
diphtheria-
tetanus-acellular
pertussis (
DTaP) vaccine, a better understanding of
vaccine-induced immune responses to Bordetella pertussis is needed. We investigated the antibody, cell-mediated, and
cytokine responses to B.
pertussis antigens in children who received the primary vaccination series (at 2, 4, and 6 months) and first booster vaccination (at 15 to 18 months) with 5-component acellular
pertussis (aP)
vaccine. The majority of subjects demonstrated a 4-fold increase in antibody titer to all four
pertussis antigens (
pertussis toxin [PT],
pertactin [PRN], filamentous
hemagglutinin [FHA], and fimbriae [FIM]) following the primary series and booster vaccination. Following the primary
vaccine series, the majority of subjects (52 to 67%) mounted a positive T cell proliferative response (stimulation index of ≥ 3) to the PT and PRN
antigens, while few subjects (7 to 12%) mounted positive proliferative responses to FHA and FIM. One month after booster vaccination (age 16 to 19 months), our study revealed significant increase in
gamma interferon (IFN-γ) production in response to the PT and FIM
antigens, a significant increase in
IL-2 production with the PT, FHA, and PRN
antigens, and a lack of significant
interleukin-4 (IL-4) secretion with any of the
antigens. While previous reports documented a mixed Th1/Th2 or Th2-skewed response to
DTaP vaccine in children, our data suggest that following the first DTaP booster, children aged 16 to 19 months have a
cytokine profile consistent with a Th1 response, which is known to be essential for clearance of
pertussis infection. To better define aP-induced immune responses following the booster
vaccine, further studies are needed to assess
cytokine responses pre- and postbooster in DTaP recipients.