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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Th1, Th17, and Th1Th17 Lymphocytes during Tuberculosis: Th1 Lymphocytes Predominate and Appear as Low-Differentiated CXCR3(+)CCR6(+) Cells in the Blood and Highly Differentiated CXCR3(+/-) CCR6(-) Cells in the Lungs
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Th1, Th17, and Th1Th17 Lymphocytes during Tuberculosis: Th1 Lymphocytes Predominate and Appear as Low-Differentiated CXCR3(+)CCR6(+) Cells in the Blood and Highly Differentiated CXCR3(+/-) CCR6(-) Cells in the Lungs

机译:结核期间Th1,Th17和Th117淋巴细胞:Th1淋巴细胞占主导地位,在肺中血液和高度分化的CXCR3(+/)CCR6(+)CCR6(+)CCR6(+)CCR6(+)细胞占优势

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摘要

Th1 lymphocytes are considered the main mediators of protection against tuberculosis (TB); however, their phenotypic characteristics and relationship with Th17 and Th1Th17 populations during TB are poorly understood. We have analyzed Th1, Th17, and Th1Th17 lymphocytes in the blood and pulmonary lesions of TB patients. The populations were identified based on the production of IFN-gamma and/or IL-17 and the coexpression of CXCR3 (X3) and CCR6 (R6). In the blood, IL-17(+) and IFN-gamma+IL-17(+)lymphocytes were barely detectable (median, 0.01% of CD4(+) lymphocytes), whereas IFN-gamma(+) lymphocytes predominated (median, 0.45%). Most IFN-gamma(+) lymphocytes (52%) were X3(+)R6(+), suggesting their "nonclassical" (ex-Th17) nature. In the lungs, IL-17(+) and IFN-gamma+IL-17(+) lymphocytes were more frequent (0.3%, p 0.005), yet IFN-gamma(+) cells predominated (11%). Phenotypically, lung CD4(+) cells were X3(+/lo)R6(-). The degree of differentiation of blood effector CD4(+) lymphocytes (evaluated based on CD62L/CD27/CD28 coexpression) increased as follows: X3(+)R6(+) X3(+)R6(-) X3(-)R6(-), with X3(-)R6(-) cells being largely terminally differentiated CD62L(-)CD27(-)CD28(-) cells. Lung CD4(+) lymphocytes were highly differentiated, recalling blood X3(+/-)R6(-) populations. Following in vitro stimulation with anti-CD3/anti-CD28 Abs, X3(+)R6(+)CD4(+) lymphocytes converted into X3(+)R6(-) and X3(-)R6(-) cells. The results demonstrate that, during active TB, Th1 lymphocytes predominate in blood and lungs, document differences in X3/R6 expression by blood and lung CD4(+) cells, and link the pattern of X3/R6 expression with the degree of cell differentiation. These findings add to the understanding of immune mechanisms operating during TB and are relevant for the development of better strategies to control it.
机译:Th1淋巴细胞被认为是针对结核病(TB)的主要介质;然而,它们在结核病期间与Th17和Th117种群的表型特征和关系很差。我们在TB患者的血液和肺部病变中分析了TH1,TH17和TH117淋巴细胞。基于IFN-Gamma和/或IL-17的产生和CXCR3(X3)和CCR6(R6)的共表达鉴定了群体。在血液中,IL-17(+)和IFN-gamma + IL-17(+)淋巴细胞几乎无法检测到(中值,& 0.01%的CD4(+)淋巴细胞),而IFN-Gamma(+)淋巴细胞占主导地位(中位数,0.45%)。大多数IFN-Gamma(+)淋巴细胞(52%)为X3(+)R6(+),表明其“非分类”(前TH17)性质。在肺中,IL-17(+)和IFN-Gamma + IL-17(+)淋巴细胞更频繁(0.3%,P <0.005),但IFN-γ(+)细胞以占优势(11%)。表型,肺CD4(+)细胞是X3(+ / LO)R6( - )。血清效应器CD4(+)淋巴细胞的分化程度(基于CD62L / CD27 / CD28共表达评估)如下:X3(+)R6(+)& X3(+)R6( - )& X3( - )R6( - ),具有X3( - - )R6( - )细胞的主要终端分化的CD62L( - )CD27( - )CD28( - )CD28( - )细胞。肺CD4(+)淋巴细胞高度分化,召回血液X3(+/-)R6( - )群。在用抗CD3 /抗CD28 ABS体外刺激之后,将X3(+)R6(+)CD4(+)淋巴细胞转化为X3(+)R6( - )和X3( - )R6( - )细胞。结果表明,在活性TB期间,Th1淋巴细胞占血液和肺部,血液和肺CD4(+)细胞的X3 / R 6表达的文件差异,并将X3 / R 6表达的模式与细胞分化的程度联系起来。这些调查结果增加了对TB期间运行的免疫机制的理解,并与控制它的更好策略的发展有关。

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