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肝片吸虫:利用合成肽鉴定11.5 kDa类鞘脂激活蛋白样蛋白SAP-2中的CD4+辅助性T细胞表位

Fasciola hepatica: identification of CD4+ T-helper epitopes from the 11.5 kDa saposin-like protein SAP-2 using synthetic peptides.

作者信息

Espino Ana M, Torres Daricel, Morales Adelaida, Delgado Bonnibel, Quetel Julia, Osuna Antonio

机构信息

University of Puerto Rico, School of Medicine, Laboratory of Molecular Parasitology and Immunology, Department of Microbiology and Medical Zoology, Office A-302, PO Box 365067, San Juan, PR 00936-5067, Puerto Rico.

出版信息

Exp Parasitol. 2007 Sep;117(1):65-73. doi: 10.1016/j.exppara.2007.03.012. Epub 2007 Mar 27.

Abstract

Fasciola hepatica saposin-like protein (FhSAP-2) is a novel antigen expressed at an early stage of infection and has been shown to induce in rabbits a significant protection to infection with F. hepatica. There are no studies to identify the immunologically relevant regions of FhSAP-2. In this work the amino acid sequence of FhSAP-2 was analyzed to identify potential T-cell epitopes. A predictive algorithm identified four possible sites. Experimental determination of the T-cell epitopes was achieved using a panel of overlapping peptides spanning the entire sequence of FhSAP-2, which was evaluated for their ability to induce lymphoproliferative responses of spleen cells from 8 immunized BALB/c (H-2d) mice. Five different epitopes were identified. There was minimal agreement between theoretical and experimental approaches. It was found that peptides containing amino acid residues AVTFA and IDIDLCDICT as part of their structure induce high levels of IL-2 and IFNgammain vitro and was classified as Th1 epitopes. Peptides that contain the residues ADQTV, CIEFVQQEVD and YIIDHVDQHN induced significant amount of IL-4 and IL-2 were considered as containers of Th0 epitopes. Identification of prominent T-cell epitopes from FhSAP-2 offers the possibility of understanding how the CD4+ T-cell response is involved in protection against fasciolosis and how it is implicated in susceptibility to infection.

摘要

肝片吸虫类鞘脂激活蛋白样蛋白(FhSAP - 2)是一种在感染早期表达的新型抗原,已证明其能使兔子对肝片吸虫感染产生显著的保护作用。目前尚无研究鉴定FhSAP - 2的免疫相关区域。在本研究中,对FhSAP - 2的氨基酸序列进行了分析,以确定潜在的T细胞表位。一种预测算法确定了四个可能的位点。通过使用一组覆盖FhSAP - 2整个序列的重叠肽来实现T细胞表位的实验测定,评估这些肽诱导8只免疫的BALB/c(H - 2d)小鼠脾细胞淋巴细胞增殖反应的能力。鉴定出了五个不同的表位。理论方法与实验方法之间的一致性极小。发现其结构中包含氨基酸残基AVTFA和IDIDLCDICT的肽在体外可诱导高水平的IL - 2和IFNγ,被归类为Th1表位。包含残基ADQTV、CIEFVQQEVD和YIIDHVDQHN且诱导大量IL - 4和IL - 2的肽被视为Th0表位的载体。鉴定FhSAP - 2突出的T细胞表位为理解CD4 + T细胞反应如何参与对肝片吸虫病的保护以及如何与感染易感性相关提供了可能性。

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