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首页> 外文期刊>Infection and immunity >Epitopes of the Onchocerca volvulus RAL1 antigen, a member of the calreticulin family of proteins, recognized by sera from patients with onchocerciasis.
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Epitopes of the Onchocerca volvulus RAL1 antigen, a member of the calreticulin family of proteins, recognized by sera from patients with onchocerciasis.

机译:盘尾丝虫蛋白CALreticulin家族成员之一的盘尾丝虫RAL1抗原的抗原决定簇,被盘尾丝虫病患者的血清所识别。

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摘要

RAL1 is an antigen (Ag) encoded by the filarial nematode Onchocerca volvulus, the parasite causing onchocerciasis (river blindness). RAL1 shares 64.4% identity with the autoantigen calreticulin. The striking similarity of the parasite Ag and the human autoantigen has led to the hypothesis that RAL1 may induce a cross-reactive immune response to calreticulin, which in turn may be involved in the pathogenesis of onchocerciasis. To test this hypothesis, we explored the immune response to RAL1 recombinant Ag (RAL1 rAg) and human calreticulin in patients with O. volvulus infection. A total of 86% of the O. volvulus-infected individuals produced antibodies recognizing RAL1 rAg. Antibody reactivity to RAL1 rAg in patient sera was confined primarily to the central and carboxyl-terminal parts of the molecule. No significant correlations were found to associate recognition of RAL1 rAg, or any particular portion thereof, with a particular disease state. Antibodies against RAL1 thus appear to be produced as a general immune reaction to O. volvulus infection and do not necessarily lead to a cross-reacting response with the host protein. In contrast, 33% of the patient sera tested bound recombinant human calreticulin. All of these sera also recognized a polypeptide encompassing the carboxyl-terminal portion of the RAL1 rAg. These results suggest that recognition of an epitope encoded in the carboxyl-terminal portion of RAL1 is at least in part responsible for inducing a cross-reacting immune response to the host protein.
机译:RAL1是由丝虫线虫Onchocerca volvulus编码的抗原(Ag),该寄生虫会引起盘尾丝虫病(河盲)。 RAL1与自身抗原钙网蛋白具有64.4%的同一性。寄生虫Ag和人类自身抗原的惊人相似性导致了这样一个假设,即RAL1可能诱导对钙网蛋白的交叉反应性免疫反应,而这又可能参与了盘尾丝虫病的发病机理。为了验证该假设,我们探讨了肠弯曲杆菌感染患者对RAL1重组Ag(RAL1 rAg)和人钙网蛋白的免疫反应。共有86%的被肠曲霉感染的个体产生了识别RAL1 rAg的抗体。患者血清中对RAL1 rAg的抗体反应性主要限于该分子的中央和羧基末端。未发现将RAL1 rAg或其任何特定部分的识别与特定疾病状态相关联的显着相关性。因此,针对RAL1的抗体似乎是作为对肠弯曲杆菌感染的一般免疫反应而产生的,并不一定导致与宿主蛋白的交叉反应。相反,有33%的患者血清结合了重组人钙网蛋白。所有这些血清也都识别了包含RAL1 rAg羧基末端部分的多肽。这些结果表明,对在RAL1的羧基末端部分编码的表位的识别至少部分负责引起对宿主蛋白的交叉反应免疫应答。

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