Pettini Elena, Pastore Gabiria, Fiorino Fabio, Medaglini Donata, Ciabattini Annalisa
Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
Vaccines (Basel). 2021 Mar 20;9(3):289. doi: 10.3390/vaccines9030289.
Characterizing the impact of the vaccination schedule on the induction of B and T cell immune responses is critical for improving vaccine immunogenicity. Here we compare the effect of a short (4 weeks) or a long (18 weeks) interval between priming and boosting in mice, using a model vaccine formulation based on the chimeric tuberculosis vaccine antigen H56 combined with alum. While no significant difference was observed in serum antigen-specific IgG response and the induction of antigen-specific T follicular helper cells into draining lymph nodes after the two immunization schedules, a longer interval between priming and boosting elicited a higher number of germinal center-B cells and H56-specific antibody-secreting cells and modulated the effector function of reactivated CD4+ T cells. These data show that the scheduling of the booster immunization could affect the immune response elicited by vaccination modulating and improving the immunogenicity of the vaccine.
确定疫苗接种程序对B细胞和T细胞免疫反应诱导的影响对于提高疫苗免疫原性至关重要。在此,我们使用基于嵌合结核疫苗抗原H56与明矾组合的模型疫苗制剂,比较了小鼠初次免疫和加强免疫之间短间隔(4周)或长间隔(18周)的效果。虽然在两种免疫程序后,血清抗原特异性IgG反应以及引流淋巴结中抗原特异性T滤泡辅助细胞的诱导方面未观察到显著差异,但初次免疫和加强免疫之间较长的间隔引发了更多数量的生发中心B细胞和H56特异性抗体分泌细胞,并调节了重新激活的CD4+T细胞的效应功能。这些数据表明,加强免疫的接种程序可通过调节和改善疫苗的免疫原性来影响疫苗接种引发的免疫反应。