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鼠伤寒沙门氏菌中负责干扰MHC I类分子上肽呈递的基因鉴定:缺失yej的沙门氏菌突变体诱导更强的CD8 + T细胞反应。

Identification of Salmonella typhimurium genes responsible for interference with peptide presentation on MHC class I molecules: Deltayej Salmonella mutants induce superior CD8+ T-cell responses.

作者信息

Qimron Udi, Madar Neta, Mittrücker Hans-Willi, Zilka Alon, Yosef Ido, Bloushtain Noga, Kaufmann Stefan H E, Rosenshine Ilan, Apte Ron N, Porgador Angel

机构信息

Department of Microbiology and Immunology, Faculty of Health Sciences and the Cancer Research Center, Ben Gurion University of the Negev, 84105 Beer Sheva, Israel.

出版信息

Cell Microbiol. 2004 Nov;6(11):1057-70. doi: 10.1111/j.1462-5822.2004.00418.x.

Abstract

Salmonella-derived epitopes are presented on MHC molecules by antigen-presenting cells, and both CD4+ and CD8+ T cells participate in protective immunity to Salmonella. Therefore, mechanisms that allow Salmonella to escape specific immune recognition are likely to have evolved in this bacterial pathogen. To identify Salmonella genes, which potentially interfere with the MHC class I (MHC-I) presentation pathway, Tn10d transposon mutagenesis was performed. More than 3000 mutants, statistically covering half of the Salmonella genome, were individually screened for altered peptide presentation by infected macrophages. Two mutants undergoing enhanced antigen presentation by macrophages were identified, carrying a Tn10d insertion in the yej operon. This phenotype was validated by specific inactivation and complementation experiments. In accordance with their enhanced MHC-I presentation phenotype, we showed that (i) specific CD8+ T cells were elicited at a higher level in mice, in response to immunization with yej mutants compared to their parental strain in two different experimental settings; and (ii) yej mutants were superior vaccine carriers for heterologous antigens compared to the parental strain in a tumour model.

摘要

沙门氏菌衍生的表位由抗原呈递细胞呈递于主要组织相容性复合体(MHC)分子上,CD4⁺和CD8⁺ T细胞均参与对沙门氏菌的保护性免疫。因此,沙门氏菌逃避特异性免疫识别的机制很可能已在这种细菌病原体中演化形成。为了鉴定可能干扰MHC I类(MHC-I)呈递途径的沙门氏菌基因,进行了Tn10d转座子诱变。通过感染的巨噬细胞对3000多个突变体(从统计学角度覆盖沙门氏菌基因组的一半)进行了单独筛选,以寻找肽呈递改变的突变体。鉴定出两个巨噬细胞抗原呈递增强的突变体,它们在yej操纵子中有一个Tn10d插入。通过特异性失活和互补实验验证了该表型。根据其增强的MHC-I呈递表型,我们发现:(i)在两种不同的实验条件下,与亲代菌株相比,用yej突变体免疫小鼠时,能更高水平地诱导出特异性CD8⁺ T细胞;(ii)在肿瘤模型中,与亲代菌株相比,yej突变体作为异源抗原的疫苗载体更具优势。

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