Transcriptional profile of tuberculosis antigen-specific T cells reveals novel multifunctional features.

Transcriptional profile of tuberculosis antigen-specific T cells reveals novel multifunctional features.
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DOI:
10.4049/jimmunol.1401151
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发表时间:
2014-09-15
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
通讯作者:
Peters B
Peters B
中科院分区:
其他
文献类型:
--
作者:
Arlehamn CL;Seumois G;Gerasimova A;Huang C;Fu Z;Yue X;Sette A;Vijayanand P;Peters B

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In latent tuberculosis infection (LTBI) spread of the bacteria is contained by a persistent immune response, which includes CD4+ T cells as important contributors. Here we show that TB-specific CD4+ T cells have a characteristic chemokine expression signature (CCR6+CXCR3+CCR4−), and that the overall number of these cells is significantly increased in LTBI donors compared to healthy subjects. We have comprehensively characterized the transcriptional signature of CCR6+CXCR3+CCR4− cells and find significant differences to conventional Th1, Th17 and Th2 cells, but no major changes between healthy and LTBI donors. CCR6+CXCR3+CCR4− cells display linage-specific signatures of both Th1 and Th17 cells, but also have a unique gene expression program including genes associated with susceptibility to TB, enhanced T cell activation, enhanced cell survival, and induction of a cytotoxic program akin to CTL cells. Overall, the gene expression signature of CCR6+CXCR3+CCR4− cells reveals characteristics important for controlling latent TB infections.
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影响因子: --
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