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Natural killer cells display impaired responses to toll like receptor 9 that support viral persistence in chronic hepatitis B

机译:自然杀伤细胞对类似受体9的通行费反应减弱,支持慢性乙型肝炎病毒的持久性

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Toll like receptors (TLR) are crucial mediators of innate immune responses, but their influence on natural killer (NK) cell function in chronic hepatitis B infection (CHB) is not well understood. Here we evaluated the responses of peripheral NK cells from CHB patients to multiple TLR agonists. CHB was associated with an impaired NK cell IFN-gamma response to TLR9 stimulation compared to controls. This deficiency corrected with recombinant IFN-alpha, while anti-IFN-alpha neutralizing antibody diminished NK IFN-gamma production in controls. NK cell CD69 upregulation in response to TLR9 was maintained in CHB. No differences were noted in responses to the other TLR ligands. Our results demonstrate a dichotomous NK cell response to TLR9 that is mediated by IFN-alpha and reflect the multiple mechanisms involved with NK activation. Consequently, it is possible that when activated these cells are unable to contribute to viral clearance while still having the potential to mediate tissue injury. (C) 2012 Elsevier Inc. All rights reserved.
机译:类似Toll样受体(TLR)是先天免疫反应的关键介体,但对慢性乙型肝炎感染(CHB)中自然杀伤(NK)细胞功能的影响尚不清楚。在这里,我们评估了CHB患者外周血NK细胞对多种TLR激动剂的反应。与对照组相比,CHB与对TLR9刺激的NK细胞IFN-γ应答受损有关。用重组IFN-α纠正了这一缺陷,而抗-IFN-α中和抗体减少了对照组中NKIFN-γ的产生。 CHB维持响应TLR9的NK细胞CD69上调。在对其他TLR配体的反应中未观察到差异。我们的结果证明了由IFN-α介导的对TLR9的二分型NK细胞反应,反映了与NK激活有关的多种机制。因此,可能的是,这些细胞在激活后无法促进病毒清除,同时仍然具有介导组织损伤的潜力。 (C)2012 Elsevier Inc.保留所有权利。

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