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首页> 外文期刊>Infection and immunity >Anaplasma marginale Major Surface Protein 2 CD4+-T-Cell Epitopes Are Evenly Distributed in Conserved and Hypervariable Regions (HVR), Whereas Linear B-Cell Epitopes Are Predominantly Located in the HVR
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Anaplasma marginale Major Surface Protein 2 CD4+-T-Cell Epitopes Are Evenly Distributed in Conserved and Hypervariable Regions (HVR), Whereas Linear B-Cell Epitopes Are Predominantly Located in the HVR

机译:边缘无浆膜主要表面蛋白2 CD4 + -T细胞表位均匀分布在保守和高变区(HVR),而线性B细胞表位主要位于HVR

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Organisms in the genus Anaplasma express an immunodominant major surface protein 2 (MSP2), composed of a central hypervariable region (HVR) flanked by highly conserved regions. Throughout Anaplasma marginale infection, recombination results in the sequential appearance of novel MSP2 variants and subsequent control of rickettsemia by the immune response, leading to persistent infection. To determine whether immune evasion and selection for variant organisms is associated with a predominant response against HVR epitopes, T-cell and linear B-cell epitopes were localized by measuring peripheral blood gamma interferon-secreting cells, proliferation, and antibody binding to 27 overlapping peptides spanning MSP2 in 16 cattle. Similar numbers of MSP2-specific CD4+ T-cell epitopes eliciting responses of similar magnitude were found in conserved and hypervariable regions. T-cell epitope clusters recognized by the majority of animals were identified in the HVR (amino acids [aa] 171 to 229) and conserved regions (aa 101 to 170 and 272 to 361). In contrast, linear B-cell epitopes were concentrated in the HVR, residing within hydrophilic sequences. The pattern of recognition of epitope clusters by T cells and of HVR epitopes by B cells is consistent with the influence of protein structure on epitope recognition.
机译:<等>类属中的生物体表达一种免疫优势的主要表面蛋白2(MSP2),该蛋白由中央高变区(HVR)和两侧的高度保守区组成。在整个无浆膜感染中,重组导致顺序出现新的MSP2变体,并随后通过免疫反应控制了立克次氏血症,导致持续感染。为了确定对变异生物体的免疫逃避和选择是否与对HVR表位的主要反应有关,通过测量外周血分泌γ干扰素的细胞,增殖以及与27种重叠肽结合的抗体来定位T细胞和线性B细胞表位跨越16头牛的MSP2。在保守区和高变区中发现了类似数量的MSP2特异性CD4 + T细胞表位,引发了相似程度的反应。在HVR(氨基酸[aa] 171至229)和保守区(aa 101至170和272至361)中鉴定出大多数动物识别的T细胞表位簇。相反,线性B细胞表位集中在HVR中,位于亲水序列中。 T细胞识别抗原决定簇簇和B细胞识别HVR抗原决定簇的方式与蛋白质结构对抗原决定簇识别的影响是一致的。

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