Staska Lauren M, Davies Christopher J, Brown Wendy C, McGuire Travis C, Suarez Carlos E, Park Joo Youn, Mathison Bruce A, Abbott Jeffrey R, Baszler Timothy V
Department of Veterinary Microbiology and Pathology, Bustad Hall, Washington State University, Pullman, WA 99164-7040, USA.
Infect Immun. 2005 Mar;73(3):1321-9. doi: 10.1128/IAI.73.3.1321-1329.2005.
Previously, our laboratory showed that Holstein cattle experimentally infected with Neospora caninum develop parasite-specific CD4+ cytotoxic T lymphocytes (CTL) that lyse infected, autologous target cells through a perforin-granzyme pathway. To identify specific parasite antigens inducing bovine CTL and helper T-lymphocyte responses for vaccine development against bovine neosporosis, the tachyzoite major surface proteins NcSAG1 and NcSRS2 were targeted. In whole tachyzoite antigen-expanded bovine T-lymphocyte lines, recombinant NcSRS2 induced potent memory CD4+- and CD8+-T-lymphocyte activation, as indicated by proliferation and gamma interferon (IFN-gamma) secretion, while recombinant NcSAG1 induced a minimal memory response. Subsequently, T-lymphocyte epitope-bearing peptides of NcSRS2 were mapped by using overlapping peptides covering the entire NcSRS2 sequence. Four experimentally infected cattle with six different major histocompatibility complex (MHC) class II haplotypes were the source of immune cells used to identify NcSRS2 peptides presented by Holstein MHC haplotypes. NcSRS2 peptides were mapped by using IFN-gamma secretion by rNcSRS2-stimulated, short-term T-lymphocyte cell lines, IFN-gamma enzyme-linked immunospot (ELISPOT) assay with peripheral blood mononuclear cells, and 51Cr release cytotoxicity assay of rNcSRS2-stimulated effector cells. Four N. caninum-infected Holstein cattle developed NcSRS2 peptide-specific T lymphocytes detected ex vivo in peripheral blood by IFN-gamma ELISPOT and in vitro by measuring T-lymphocyte IFN-gamma production and cytotoxicity. An immunodominant region of NcSRS2 spanning amino acids 133 to 155 was recognized by CD4+ T lymphocytes from the four cattle. These findings support investigation of subunit N. caninum vaccines incorporating NcSRS2 gene sequences or peptides for induction of NcSRS2 peptide-specific CTL and IFN-gamma-secreting T lymphocytes in cattle with varied MHC genotypes.
此前,我们的实验室表明,实验感染犬新孢子虫的荷斯坦奶牛会产生寄生虫特异性CD4 + 细胞毒性T淋巴细胞(CTL),这些细胞通过穿孔素-颗粒酶途径裂解被感染的自体靶细胞。为了鉴定诱导牛CTL和辅助性T淋巴细胞反应的特定寄生虫抗原,以用于开发抗牛新孢子虫病疫苗,我们将速殖子主要表面蛋白NcSAG1和NcSRS2作为目标。在全速殖子抗原扩增的牛T淋巴细胞系中,重组NcSRS2诱导了有效的记忆性CD4 + 和CD8 + T淋巴细胞活化,这通过增殖和γ干扰素(IFN-γ)分泌得以体现,而重组NcSAG1诱导的记忆反应则很微弱。随后,通过使用覆盖整个NcSRS2序列的重叠肽对NcSRS2的T淋巴细胞表位肽进行了定位。四只实验感染的奶牛具有六种不同的主要组织相容性复合体(MHC)II类单倍型,它们是用于鉴定荷斯坦MHC单倍型所呈递的NcSRS2肽的免疫细胞来源。通过rNcSRS2刺激的短期T淋巴细胞系分泌的IFN-γ、外周血单核细胞的IFN-γ酶联免疫斑点(ELISPOT)测定以及rNcSRS2刺激的效应细胞的51Cr释放细胞毒性测定来对NcSRS2肽进行定位。四只感染犬新孢子虫的荷斯坦奶牛产生了NcSRS2肽特异性T淋巴细胞,通过IFN-γ ELISPOT在体外检测外周血中的这些细胞,并通过测量T淋巴细胞IFN-γ的产生和细胞毒性在体外进行检测。来自这四只奶牛的CD4 + T淋巴细胞识别出了NcSRS2的一个跨越氨基酸133至155的免疫显性区域。这些发现支持对包含NcSRS2基因序列或肽的犬新孢子虫亚单位疫苗进行研究,以在具有不同MHC基因型的牛中诱导产生NcSRS2肽特异性CTL和分泌IFN-γ的T淋巴细胞。