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在病毒血症性HIV-1感染中,自然杀伤(NK)细胞的细胞溶解功能受损与自然细胞毒性受体(NKp46、NKp30和NKp44)的表面表达减少有关。

The impaired NK cell cytolytic function in viremic HIV-1 infection is associated with a reduced surface expression of natural cytotoxicity receptors (NKp46, NKp30 and NKp44).

作者信息

De Maria Andrea, Fogli Manuela, Costa Paola, Murdaca Giuseppe, Puppo Francesco, Mavilio Domenico, Moretta Alessandro, Moretta Lorenzo

机构信息

Dipartimento di Medicina Interna, University of Genoa, Genoa, Italy.

出版信息

Eur J Immunol. 2003 Sep;33(9):2410-8. doi: 10.1002/eji.200324141.

Abstract

Signals leading to NK cell triggering are primarily mediated by natural cytotoxicity receptors (NCR) upon binding to as-yet-undefined cell surface ligand(s) on normal hematopoietic cells, pathogen-infected cells or tumor cells. In this study we tried to determine whether the decreased NK cell cytolytic function that is observed in HIV-1-infected patients may be related to a decreased expression of NCR. In HIV-1-infected patients, freshly drawn, purified NK cells expressed significantly decreased surface densities of NKp46 and NKp30 NCR. The low surface density of NKp46, NKp30 and NKp44 was also confirmed in in-vitro-activated NK cell populations and NK cell clones derived from HIV-1 patients compared with uninfected donors. This defective NCR expression in HIV-1 patients was associated with a parallel decrease of NCR-mediated killing of different tumor target cells. Thus, the present study indicates that the defective expression of NCR represents at least one of the possible mechanisms leading to the impaired NK cell function in HIV-1 infection and it can contribute to explain the relatively high frequency of opportunistic tumors reported in cohorts of untreated patients before the occurrence of profound immunosuppression (<200 CD4(+) cells/mm(3)).

摘要

导致自然杀伤(NK)细胞触发的信号主要由自然细胞毒性受体(NCR)介导,这些受体与正常造血细胞、病原体感染细胞或肿瘤细胞表面尚未明确的配体结合。在本研究中,我们试图确定在人类免疫缺陷病毒1型(HIV-1)感染患者中观察到的NK细胞溶解功能下降是否可能与NCR表达降低有关。在HIV-1感染患者中,新鲜提取并纯化的NK细胞表达的NKp46和NKp30 NCR表面密度显著降低。与未感染的供体相比,在HIV-1患者来源的体外激活的NK细胞群体和NK细胞克隆中,NKp46、NKp30和NKp44的低表面密度也得到了证实。HIV-1患者中这种有缺陷的NCR表达与NCR介导的对不同肿瘤靶细胞杀伤作用的平行下降有关。因此,本研究表明,NCR表达缺陷代表了HIV-1感染中导致NK细胞功能受损的至少一种可能机制,并且它有助于解释在未治疗患者队列中,在出现严重免疫抑制(<200个CD4(+)细胞/mm(3))之前报告的机会性肿瘤相对较高的发生率。

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