首页> 外文期刊>Infection and immunity >Identification of Vaccine Candidate Peptides in the NcSRS2 Surface Protein of Neospora caninum by Using CD4+ Cytotoxic T Lymphocytes and Gamma Interferon-Secreting T Lymphocytes of Infected Holstein Cattle
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Identification of Vaccine Candidate Peptides in the NcSRS2 Surface Protein of Neospora caninum by Using CD4+ Cytotoxic T Lymphocytes and Gamma Interferon-Secreting T Lymphocytes of Infected Holstein Cattle

机译:利用感染的荷斯坦牛的CD4 +细胞毒性T淋巴细胞和γ干扰素分泌的T淋巴细胞鉴定新孢子虫NcSRS2表面蛋白中的疫苗候选肽

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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-γ) 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-γ secretion by rNcSRS2-stimulated, short-term T-lymphocyte cell lines, IFN-γ 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-γ ELISPOT and in vitro by measuring T-lymphocyte IFN-γ 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-γ-secreting T lymphocytes in cattle with varied MHC genotypes.
机译:以前,我们的实验室表明,实验感染了 Neospora caninum 的荷斯坦牛会产生寄生虫特异性CD4 + 细胞毒性T淋巴细胞(CTL),该蛋白通过穿孔素裂解被感染的自体靶细胞。颗粒酶途径。为了鉴定诱导牛CTL和辅助T淋巴细胞反应的特定寄生虫抗原,以开发针对牛新孢子虫病的疫苗,靶向速殖子主要表面蛋白NcSAG1和NcSRS2。在整个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CD4 + -和CD8 + -T淋巴细胞活化,如增殖和γ干扰素所示。 (IFN-γ)分泌,而重组NcSAG1诱导了最小的记忆反应。随后,通过使用覆盖整个NcSRS2序列的重叠肽对NcSRS2的带有T淋巴细胞抗原决定簇的肽作图。具有六种不同的主要组织相容性复合体(MHC)II类单倍型的四只经实验感染的牛是用于鉴定Holstein MHC单倍型呈递的NcSRS2肽的免疫细胞的来源。使用rNcSRS2刺激的短期T淋巴细胞细胞系,外周血单个核细胞的IFN-γ酶联免疫斑点(ELISPOT)分析和 51 ,通过IFN-γ分泌来绘制NcSRS2肽rNcSRS2刺激的效应细胞的Cr释放细胞毒性测定。四个 N。被犬感染的荷斯坦牛开发了NcSRS2肽特异性T淋巴细胞,通过IFN-γELISPOT在离体血液中进行体外检测,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了检测。来自四头牛的CD4 + T淋巴细胞识别出NcSRS2的一个免疫优势区域,该区域位于133至155位氨基酸之间。这些发现支持对亚基 N的研究。包含NcSRS2基因序列或肽的犬疫苗,用于在具有不同MHC基因型的牛中诱导NcSRS2肽特异性CTL和分泌IFN-γ的T淋巴细胞。

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