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全血检测中依赖于 FcγRIIIa 的 IFN-γ 释放可预测治疗性 IgG1 抗体的安全性。

FcγRIIIa-dependent IFN-γ release in whole blood assay is predictive of therapeutic IgG1 antibodies safety.

机构信息

a Lilly Research Laboratories , A Division of Eli Lilly and Company , Indianapolis , IN , USA.

出版信息

MAbs. 2018 Aug/Sep;10(6):913-921. doi: 10.1080/19420862.2018.1474996. Epub 2018 Jul 26.

DOI:10.1080/19420862.2018.1474996
PMID:29953319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6152447/
Abstract

Immunomodulatory monoclonal IgG1 antibodies developed for cancer and autoimmune disease have an inherent risk of systemic release of pro-inflammatory cytokines. In vitro cytokine release assays are currently used to predict cytokine release syndrome (CRS) risk, but the validation of these preclinical tools suffers from the limited number of characterized CRS-inducing IgG1 antibodies and the poor understanding of the mechanisms regulating cytokine release. Here, we incubated human whole blood from naïve healthy volunteers with four monoclonal IgG1 antibodies with different proven or predicted capacity to elicit CRS in clinic and measured cytokine release using a multiplex assay. We found that, in contrast to anti-CD52 antibodies (Campath-1H homolog) that elicited high level of multiple inflammatory cytokines from human blood cells in vitro, other IgG1 antibodies with CRS-inducing potential consistently induced release of a single tested cytokine, interferon (IFN)-γ, with a smaller magnitude than Campath. IFN-γ expression was observed as early as 2-4 h after incubation, mediated by natural killer cells, and dependent upon tumor necrosis factor and FcγRIII. Importantly, the magnitude of the IFN-γ response elicited by IgG1 antibodies with CRS-inducing potential was determined by donor FcγRIIIa-V158F polymorphism. Overall, our results highlight the importance of FcγRIIIa-dependent IFN-γ release in preclinical cytokine release assay for the prediction of CRS risk associated with therapeutic IgG1 antibodies.

摘要

为癌症和自身免疫性疾病开发的免疫调节单克隆 IgG1 抗体具有全身释放促炎细胞因子的固有风险。目前,细胞因子释放试验(Cytokine Release Assay,CRA)被用于预测细胞因子释放综合征(Cytokine Release Syndrome,CRS)风险,但这些临床前工具的验证受到以下因素的限制:具有特征性的能够诱导 CRS 的 IgG1 抗体数量有限,以及对调节细胞因子释放的机制的理解不足。在这里,我们将来自 naive 健康志愿者的全血与四种单克隆 IgG1 抗体孵育,这些抗体具有不同的在临床上引起 CRS 的能力或预测能力,并使用多重分析来测量细胞因子的释放。我们发现,与能够在体外从人血细胞中引发高水平多种炎症细胞因子的抗 CD52 抗体(Campath-1H 同源物)相比,具有 CRS 诱导潜力的其他 IgG1 抗体一致地诱导了单一测试细胞因子 IFN-γ的释放,其幅度小于 Campath。IFN-γ 的表达早在孵育后 2-4 小时即可观察到,由自然杀伤细胞介导,并依赖于肿瘤坏死因子和 FcγRIII。重要的是,具有 CRS 诱导潜力的 IgG1 抗体引发的 IFN-γ 反应的幅度取决于供体 FcγRIIIa-V158F 多态性。总的来说,我们的结果强调了 FcγRIIIa 依赖性 IFN-γ 释放在预测与治疗性 IgG1 抗体相关的 CRS 风险的临床前细胞因子释放试验中的重要性。