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对纯化曼氏血吸虫抗原免疫应答的遗传控制。II. 特异性I-A和I-E限制性T细胞克隆的建立与特性分析

Genetic control of immune response to a purified Schistosoma mansoni antigen. II. Establishment and characterization of specific I-A and I-E restricted T-cell clones.

作者信息

Mendlovic F, Arnon R, Tarrab-Hazdai R, Puri J

机构信息

Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Parasite Immunol. 1989 Nov;11(6):683-94. doi: 10.1111/j.1365-3024.1989.tb00929.x.

DOI:10.1111/j.1365-3024.1989.tb00929.x
PMID:2515517
Abstract

T-cell lines and clones specific for a partially protective schistosome antigen (9B antigen) were established from mice immunized with such antigen. The H-2 congenic strains B10.A which express both I-A and I-E class II gene products of the major histocompatibility complex (MHC) and B10.A(4R) which only express I-A molecules were used in these studies. The specific T-cell lines recognized the 9B antigen in the context of either A or E molecules, but both class II antigens were necessary for maximal stimulation of the T-cell lines in lymphocyte proliferation assays. T-cell clones were derived from these lines and their MHC restriction was investigated. Both I-A and I-E restricted clones could be isolated. All clones were specific for 9B antigen showing different degrees of cross-reactivity with a total schistosome extract (CA sonicate). A correlation between the fine specificity of the clones and the expression of class II antigens was demonstrated. Clones specific for 9B antigen, or which reacted to the same extent with 9B antigen and CA sonicate, were I-A restricted, whereas clones which proliferated more in the presence of CA sonicate were all I-E restricted. This suggests that I-E restricted clones recognize more cross-reactive epitopes than I-A restricted clones. These antigen-specific T-cell clones should provide a useful tool for examining the role of class II antigens in the modulation of protective immune response during Schistosoma mansoni infection.

摘要

用部分保护性血吸虫抗原(9B抗原)免疫小鼠后,建立了针对该抗原的T细胞系和克隆。主要组织相容性复合体(MHC)的I-A和I-E II类基因产物均表达的H-2同基因系B10.A以及仅表达I-A分子的B10.A(4R)用于这些研究。特异性T细胞系在A或E分子的背景下识别9B抗原,但在淋巴细胞增殖试验中,两种II类抗原对于T细胞系的最大刺激都是必需的。从这些细胞系中获得T细胞克隆,并研究其MHC限制性。可以分离出I-A和I-E限制性克隆。所有克隆均对9B抗原具有特异性,与血吸虫全虫提取物(CA超声裂解物)表现出不同程度的交叉反应性。证明了克隆的精细特异性与II类抗原表达之间的相关性。对9B抗原具有特异性或与9B抗原和CA超声裂解物反应程度相同的克隆是I-A限制性的,而在CA超声裂解物存在下增殖更多的克隆均是I-E限制性的。这表明I-E限制性克隆比I-A限制性克隆识别更多的交叉反应性表位。这些抗原特异性T细胞克隆应为研究II类抗原在曼氏血吸虫感染期间保护性免疫反应调节中的作用提供有用的工具。

相似文献

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Genetic control of immune response to a purified Schistosoma mansoni antigen. II. Establishment and characterization of specific I-A and I-E restricted T-cell clones.对纯化曼氏血吸虫抗原免疫应答的遗传控制。II. 特异性I-A和I-E限制性T细胞克隆的建立与特性分析
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引用本文的文献

1
A mimotope peptide-based vaccine against Schistosoma mansoni: synthesis and characterization.一种基于模拟表位肽的曼氏血吸虫疫苗:合成与表征
Immunology. 2000 Dec;101(4):555-62. doi: 10.1046/j.1365-2567.2000.00139.x.
2
Intranasal administration of synthetic recombinant peptide-based vaccine protects mice from infection by Schistosoma mansoni.经鼻给予基于合成重组肽的疫苗可保护小鼠免受曼氏血吸虫感染。
Infect Immun. 1999 Sep;67(9):4360-6. doi: 10.1128/IAI.67.9.4360-4366.1999.
3
Synthesis and characterization of a protective peptide-based vaccine against Schistosoma mansoni.
一种针对曼氏血吸虫的基于保护性肽的疫苗的合成与表征
Infect Immun. 1998 Sep;66(9):4526-30. doi: 10.1128/IAI.66.9.4526-4530.1998.