Xu-Amano J, Jackson R J, Fujihashi K, Kiyono H, Staats H F, McGhee J R
Department of Microbiology, University of Alabama at Birmingham 35294.
Vaccine. 1994 Aug;12(10):903-11. doi: 10.1016/0264-410x(94)90033-7.
We have used the potent mucosal immunogen cholera toxin (CT) to assess antigen-specific CD4+ T-cell responses, including Th1- and Th2-type cells in mucosa-associated tissues, e.g. Peyer's patches (PP), and systemic tissue, e.g. spleen (SP), for their regulatory role in the induction of CT-specific B-cell antibody responses in the gastrointestinal (GI) tract as well as in systemic sites. The CT was given by either oral or intravenous (i.v.) routes and the mice orally immunized with CT exhibited brisk IgA anti-CT antibody responses in faecal extracts and elevated IgG anti-CT antibody responses in serum. Further, significant IgA anti-CT spot-forming cells (SFCs) were seen in lamina propria lymphocytes (LPLs) from mice orally immunized with CT. In contrast, i.v. immunization with CT induced IgM and IgG anti-CT SFC responses in SP, and serum anti-CT antibodies of these two isotypes; no anti-CT responses were induced in the GI tract after immunization by this route. The CD4+ T cells isolated from PP and SP of mice orally immunized with CT were stimulated in vitro with CT-B-coated latex microspheres for 1-6 days, and the induction of IL-2 and interferon gamma (IFN-gamma) (Th1-type) or IL-4 and IL-5 (Th2-type) producing SFCs were analysed by a cytokine-specific ELISPOT and cytokine-specific mRNA was detected by reverse transcriptase (RT)-PCR assays.(ABSTRACT TRUNCATED AT 250 WORDS)
我们使用了强效黏膜免疫原霍乱毒素(CT)来评估抗原特异性CD4+ T细胞反应,包括黏膜相关组织(如派尔集合淋巴结(PP))和全身组织(如脾脏(SP))中的Th1型和Th2型细胞,以研究它们在胃肠道(GI)以及全身部位诱导CT特异性B细胞抗体反应中的调节作用。CT通过口服或静脉内(i.v.)途径给予,口服免疫CT的小鼠在粪便提取物中表现出活跃的IgA抗CT抗体反应,血清中IgG抗CT抗体反应升高。此外,在口服免疫CT的小鼠的固有层淋巴细胞(LPL)中可见大量IgA抗CT斑点形成细胞(SFC)。相比之下,静脉内免疫CT诱导脾脏中IgM和IgG抗CT SFC反应以及这两种同种型的血清抗CT抗体;通过该途径免疫后,胃肠道未诱导出抗CT反应。从口服免疫CT的小鼠的PP和SP中分离出的CD4+ T细胞,在体外用包被CT-B的乳胶微球刺激1 - 6天,通过细胞因子特异性ELISPOT分析产生IL-2和干扰素γ(IFN-γ)(Th1型)或IL-4和IL-5(Th2型)的SFC的诱导情况,并通过逆转录酶(RT)-PCR测定检测细胞因子特异性mRNA。(摘要截断于250字)