CD8+ T cells in Trypanosoma cruzi infection

被引:107
作者
Padilla, Angel M. [1 ]
Bustamante, Juan M. [1 ]
Tarleton, Rick L. [1 ,2 ]
机构
[1] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 USA
[2] Univ Georgia, Dept Cellular Biol, Athens, GA 30602 USA
基金
美国国家卫生研究院;
关键词
TRANS-SIALIDASE; LIMITED ROLE; MEMORY; ANTIGEN; MODULATION; IMMUNITY; DYSFUNCTION; GENERATION; RESPONSES; PROTEINS;
D O I
10.1016/j.coi.2009.07.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8(+) T cells have emerged as crucial players in the control of a number of protozoan pathogens, including Trypanosoma cruzi, the agent of human Chagas disease. The recent identification of the dominant targets of T. cruzi-specific T cells has allowed investigators to follow the generation of and document the functionality of T cell responses in both mice and humans. Although slow to develop in the early stages of the infection, T. cruzi-specific CD8(+) T cells reach prodigious levels and remain highly functional throughout chronic infections in mice. Following drug-induced cure during either the acute or chronic stage, these immunodominant T cells persist as stable, antigen-independent memory populations. T. cruzi-specific CD8(+) T cells in humans are less-well-studied but appear to lose functionality and decline in numbers in these decades-long infections. Changes in the frequency of parasite-specific T cell upon therapeutic treatment in humans may provide a new metric for determining treatment efficacy.
引用
收藏
页码:385 / 390
页数:6
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