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Mucosal‐associated invariant T cells and Vδ2+ γδ T cells in community acquired pneumonia: association of abundance in sputum with clinical severity and outcome

机译:粘膜相关的不变性T细胞和群落中获得的肺炎中的Vδ2+γδT细胞:痰中患有临床严重程度和结果的痰中的丰度结合

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摘要

Mucosal‐associated invariant T (MAIT) cells and Vδ2+ γδ T cells are anti‐bacterial innate‐like lymphocytes (ILLs) that are enriched in blood and mucosa. ILLs have been implicated in control of infection. However, the role of ILLs in community‐acquired pneumonia (CAP) is unknown. Using sputum samples from a well‐characterized CAP cohort, MAIT cell and Vδ2+ T cell abundance was determined by quantitative polymerase chain reaction (qPCR). Cytokine and chemokine concentrations in sputum were measured. The capacity of bacteria in sputum to produce activating ligands for MAIT cells and Vδ2+ T cells was inferred by 16S rRNA sequencing. MAIT cell abundance in sputum was higher in patients with less severe pneumonia; duration of hospital admission was inversely correlated with both MAIT and Vδ2+ T cell abundance. The abundance of both ILLs was higher in patients with a confirmed bacterial aetiology; however, there was no correlation with total bacterial load or the predicted capacity of bacteria to produce activating ligands. Sputum MAIT cell abundance was associated with interferon (IFN)‐α, IFN‐γ, and sputum neutrophil abundance, while Vδ2+ T cell abundance was associated with CXCL11 and IFN‐γ. Therefore, MAIT and Vδ2+ T cells can be detected in sputum in CAP, where they may contribute to improved clinical outcome.
机译:粘膜相关的不变性T(MAIT)细胞和Vδ2+γδT细胞是富含血液和粘膜的抗细菌先天样淋巴细胞(ILL)。弊病涉及对感染的控制。然而,疾病在社区获得的肺炎(帽子)中的作用是未知的。通过定量聚合酶链反应(QPCR)测定使用来自特征良好的帽坐标的痰液样品,Mait细胞和Vδ2+ T细胞丰度。测量痰中的细胞因子和趋化因子浓度。通过16S rRNA测序推断出痰中痰中的细菌在痰液中产生活化配体和Vδ2+ T细胞的能力。肺炎患者患者痰中的痰中的MAIT细胞丰度较高;医院入院的持续时间与MAIT和Vδ2+ T细胞丰富相反。确诊的细菌性病学患者的两种患者的丰富程度较高;然而,与总细菌载荷或细菌的预测能力没有相关性,以产生活化配体。痰地区细胞丰度与干扰素(IFN)-α,IFN-γ和痰中性粒细胞丰度有关,而Vδ2+ T细胞丰度与CXCL11和IFN-γ相关。因此,可以在帽中的痰中检测到MAIT和Vδ2+ T细胞,其中它们可能有助于改善临床结果。

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