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引发抗原中决定簇的分子背景建立了T细胞诱导的层次结构:由β-半乳糖苷酶肽与完整抗原诱导的T细胞特异性。

The molecular context of determinants within the priming antigen establishes a hierarchy of T cell induction: T cell specificities induced by peptides of beta-galactosidase vs. the whole antigen.

作者信息

Shivakumar S, Sercarz E E, Krzych U

机构信息

Department of Biology, Catholic University of America, Washington, DC.

出版信息

Eur J Immunol. 1989 Apr;19(4):681-7. doi: 10.1002/eji.1830190417.

Abstract

The antibody response following priming with a macromolecule or a peptide will depend on the regulatory T cells that become activated by the antigenic determinants available. In this report, activation of T helper (Th) and T suppressor (Ts) cells by determinants on beta-galactosidase (GZ) was examined by comparing native GZ [1023 amino acid (a.a.) residues per monomer] with peptides from the immunodominant region encompassing residues 3 to 187. Each immunogen established its characteristic hierarchy of dominance of determinants within it: in particular, GZ and CB-2-3 (a.a. 3-187) each induced immunodominant Th cells which could not be induced by T8 (a.a. 60-140). Hierarchies of suppressor determinant are also created: T8-Ts suppresses all Th specificities and therefore can be deemed immunodominant: T8-2-Ts and T8-3-Ts have a more selective suppressor activity and can be considered subdominant. We conclude that the outcome of immunization shifts with a change in the nature of the immunogen and the context within which the determinant lies will crucially influence its expression. A particular "context" presumably determines the likely order of processing of that molecule which leads to a characteristic relationship among the Ts, Th and B cell determinants involved.

摘要

用大分子或肽进行初次免疫后的抗体反应将取决于被可用抗原决定簇激活的调节性T细胞。在本报告中,通过比较天然β-半乳糖苷酶(GZ)[每个单体含1023个氨基酸(a.a.)残基]与来自免疫显性区域(包含3至187位残基)的肽段,研究了β-半乳糖苷酶(GZ)上的决定簇对辅助性T细胞(Th)和抑制性T细胞(Ts)的激活作用。每种免疫原在其内部都建立了其特有的决定簇优势等级:特别是,GZ和CB-2-3(3至187位氨基酸)各自诱导出的免疫显性Th细胞不能被T8(60至140位氨基酸)诱导。抑制性决定簇的等级也得以确立:T8-Ts抑制所有Th特异性,因此可被视为免疫显性;T8-2-Ts和T8-3-Ts具有更具选择性的抑制活性,可被视为亚显性。我们得出结论,免疫接种的结果会随着免疫原性质的变化而改变,并且决定簇所处的背景将对其表达产生关键影响。特定的“背景”大概决定了该分子可能的加工顺序,这导致了所涉及的Ts、Th和B细胞决定簇之间的特征性关系。

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