Department of Microbiology and Immunology and Göteborg University Vaccine Research Institute (GUVAX), University of Gothenburg, Medicinaregatan 7A, Box 435, 405 30 Gothenburg, Sweden.
Vaccine. 2010 Jul 26;28(33):5445-50. doi: 10.1016/j.vaccine.2010.06.001. Epub 2010 Jun 12.
Assessment of immune responses induced by mucosal vaccines is to a large extent based on measurement of IgA levels in mucosal secretions and detection of short-lived effector IgA-secreting cells circulating in peripheral blood. Since these immunological parameters poorly reflect long-term IgA-mediated responses, we sought to investigate novel approaches that would enable detection of vaccine specific IgA memory B cells. We demonstrate that stimulation of human peripheral blood mononuclear cells in vitro with immunostimulatory DNA in combination with B cell-activating factor (BAFF) and IL-15 promotes differentiation of IgA memory B cells to IgA-secreting cells. By using the inactivated oral cholera vaccine Dukoral we demonstrate that vaccine specific IgA memory B cells are induced by oral immunization and are circulating for at least 9 months after vaccination. We also show that stimulated IgA memory B cells do not secrete IgA unless they reencounter the specific antigen.
黏膜疫苗诱导的免疫应答的评估在很大程度上基于黏膜分泌物中 IgA 水平的测量和在外周血中循环的短暂效应 IgA 分泌细胞的检测。由于这些免疫参数不能很好地反映长期 IgA 介导的应答,我们试图研究新的方法,以便能够检测疫苗特异性 IgA 记忆 B 细胞。我们证明,体外用人外周血单核细胞与免疫刺激 DNA 联合 B 细胞激活因子 (BAFF) 和 IL-15 刺激可促进 IgA 记忆 B 细胞分化为 IgA 分泌细胞。我们使用已灭活的口服霍乱疫苗 Dukoral 证明,口服免疫可诱导疫苗特异性 IgA 记忆 B 细胞,并且在接种疫苗后至少 9 个月仍在循环。我们还表明,受刺激的 IgA 记忆 B 细胞不会分泌 IgA,除非它们再次遇到特定抗原。