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首页> 外文期刊>Journal of Virological Methods >Flow cytometry-based assay to study HIV-1 gp120 specific antibody-dependent cellular cytotoxicity responses
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Flow cytometry-based assay to study HIV-1 gp120 specific antibody-dependent cellular cytotoxicity responses

机译:基于流式细胞仪的分析法研究HIV-1 gp120特异性抗体依赖性细胞的细胞毒性反应

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Increased attention on the role of Fc-mediated effector functions against HIV-1 has led to renewed interest into the role that antibody-dependent cellular cytotoxicity (ADCC) could play in controlling viral transmission and/or the rate of disease progression. While (51)Chromium release assays have traditionally been used to study ADCC responses against HIV-1, a number of alternative flow-cytometry-based assays were recently developed. In this study, an alternative flow-cytometry-based assay was established to allow non-radioactive measurement of ADCC-mediated elimination of HIV-1 gp120 envelope glycoprotein (Env)-coated target cells. This assay relies on staining target and effector cells with different dyes, which allows precise gating and permits the calculation of the number of surviving target cells by normalization to flow-cytometry particles. By using small concentrations of recombinant gp120 Env, suitable targets cells that recapitulate the ADCC response mediated against HIV-1-infected cells were generated. Finally, this method was applied successfully to screen human sera for ADCC activity directed against HIV-1 gp120 Env. (C) 2014 Elsevier B.V. All rights reserved.
机译:对Fc介导的针对HIV-1的效应子功能的作用的关注日益增加,引起了人们对抗体依赖性细胞毒性(ADCC)在控制病毒传播和/或疾病进展速度中所起的作用的重新关注。传统上(51)铬释放试验已被用于研究ADCC对HIV-1的反应,但最近开发了许多基于流式细胞术的替代试验。在这项研究中,建立了另一种基于流式细胞术的测定方法,以实现ADCC介导的HIV-1 gp120包膜糖蛋白(Env)包被靶细胞消除的非放射性测量。该测定法依赖于用不同染料对靶细胞和效应细胞进行染色,这可以实现精确的门控,并可以通过对流式细胞仪颗粒进行归一化来计算存活靶细胞的数量。通过使用低浓度的重组gp120 Env,可以产生合适的靶细胞,该靶细胞概括了针对HIV-1感染细胞介导的ADCC反应。最后,该方法成功地用于筛选人血清中针对HIV-1 gp120 Env的ADCC活性。 (C)2014 Elsevier B.V.保留所有权利。

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