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Drug-induced cure drives conversion to a stable and protective CD8+ T central memory response in chronic Chagas disease

机译:在慢性恰加斯病中药物诱导的治愈促使转化为稳定和保护性的CD8 + T中枢记忆反应

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摘要

In this study, we document the development of stable, antigen-independent CD8+ T cell memory after drug-induced cure of a chronic infection. By establishing a system for drug cure of chronic Trypanosoma cruzi infection, we present the first extensively documented case of total parasite clearance after drug treatment of this infection. Cure resulted in the emergence of a stable, parasite-specific CD8+ T cell population with the characteristics of central memory cells, based upon expression of CD62L, CCR7, CD127, CD122, Bcl-2 and a reduced immediate in vivo CTL function. CD8+ T cells from treated and cured mice also expanded more rapidly and provided greater protection following challenge than those from chronically infected mice. These results show that complete pathogen clearance results in stable, antigen-independent and protective T cell memory, despite the potentially exhausting effects of prior long-term exposure to antigen in this chronic infection.
机译:在这项研究中,我们记录了药物诱导的慢性感染治愈后稳定,独立于抗原的CD8 + T细胞记忆的发展。通过建立慢性克氏锥虫感染的药物治疗系统,我们介绍了该感染的药物治疗后首次全面记录的寄生虫清除率。根据CD62L,CCR7,CD127,CD122,Bcl-2的表达和降低的表达,治愈导致出现稳定的,具有寄生虫特异性的CD8 + T细胞群,具有中央记忆细胞的特征立即体内CTL功能。与慢性感染的小鼠相比,经治疗和治愈的小鼠的CD8 + T细胞也能更快地扩增并提供更大的保护作用。这些结果表明,尽管先前在这种慢性感染中长期暴露于抗原可能会产生疲惫的影响,但完全清除病原体仍可导致稳定的,不依赖抗原的和保护性的T细胞记忆。

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