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检查犬白细胞 IgG Fc 受体 CD16A 和 CD64 的表达及其在工程化自然杀伤 (NK) 细胞中的 ADCC 活性。

Examination of IgG Fc Receptor CD16A and CD64 Expression by Canine Leukocytes and Their ADCC Activity in Engineered NK Cells.

机构信息

Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, MN, United States.

Animal Cancer Care and Research Program, University of Minnesota, St. Paul, MN, United States.

出版信息

Front Immunol. 2022 Feb 24;13:841859. doi: 10.3389/fimmu.2022.841859. eCollection 2022.

Abstract

Human natural killer (NK) cells can target tumor cells in an antigen-specific manner by the recognition of cell bound antibodies. This process induces antibody-dependent cell-mediated cytotoxicity (ADCC) and is exclusively mediated by the low affinity IgG Fc receptor CD16A (FcγRIIIA). Exploiting ADCC by NK cells is a major area of emphasis for advancing cancer immunotherapies. CD64 (FcγRI) is the only high affinity IgG FcR and it binds to the same IgG isotypes as CD16A, but it is not expressed by human NK cells. We have generated engineered human NK cells expressing recombinant CD64 with the goal of increasing their ADCC potency. Preclinical testing of this approach is essential for establishing efficacy and safety of the engineered NK cells. The dog provides particular advantages as a model, which includes spontaneous development of cancer in the setting of an intact and outbred immune system. To advance this immunotherapy model, we cloned canine CD16A and CD64 and generated specific mAbs. We report here for the first time the expression patterns of these FcγRs on dog peripheral blood leukocytes. CD64 was expressed by neutrophils and monocytes, but not lymphocytes, while canine CD16A was expressed at high levels by a subset of monocytes and lymphocytes. These expression patterns are similar to that of human leukocytes. Based on phenotypic characteristics, the CD16A lymphocytes consisted of T cells (CD3 CD8 CD5 α/β TCR) and NK cells (CD3 CD5 CD94), but not B cells. Interestingly, the majority of canine CD16A lymphocytes were from the T cell population. Like human CD16A, canine CD16A was downregulated by a disintegrin and metalloproteinase 17 (ADAM17) upon leukocyte activation, revealing a conserved means of regulation. We also directly demonstrate that both canine CD16A and CD64 can induce ADCC when expressed in the NK cell line NK-92. These findings pave the way to engineering canine NK cells or T cells with high affinity recombinant canine CD64 to maximize ADCC and to test their safety and efficacy to benefit both humans and dogs.

摘要

人类自然杀伤 (NK) 细胞可以通过识别细胞结合抗体以抗原特异性方式靶向肿瘤细胞。这个过程诱导抗体依赖性细胞介导的细胞毒性 (ADCC),并且仅由低亲和力 IgG Fc 受体 CD16A (FcγRIIIA) 介导。利用 NK 细胞的 ADCC 是推进癌症免疫疗法的主要重点领域。CD64(FcγRI)是唯一的高亲和力 IgG FcR,它与 CD16A 结合相同的 IgG 同种型,但不表达于人类 NK 细胞。我们已经生成了表达重组 CD64 的工程化人类 NK 细胞,旨在提高其 ADCC 效力。这种方法的临床前测试对于建立工程化 NK 细胞的功效和安全性至关重要。狗作为模型具有特殊的优势,包括在完整的、远交的免疫系统背景下自发发展癌症。为了推进这种免疫疗法模型,我们克隆了犬 CD16A 和 CD64,并生成了特异性 mAb。我们首次在这里报告了这些 FcγR 在犬外周血白细胞上的表达模式。CD64 表达于中性粒细胞和单核细胞,但不表达于淋巴细胞,而犬 CD16A 则高水平表达于单核细胞和淋巴细胞的一个亚群。这些表达模式与人类白细胞相似。基于表型特征,CD16A 淋巴细胞由 T 细胞 (CD3 CD8 CD5α/β TCR) 和 NK 细胞 (CD3 CD5 CD94) 组成,但不包括 B 细胞。有趣的是,大多数犬 CD16A 淋巴细胞来自 T 细胞群体。与人类 CD16A 一样,犬 CD16A 在白细胞激活时被解整合素和金属蛋白酶 17 (ADAM17) 下调,显示出保守的调节方式。我们还直接证明,当在 NK 细胞系 NK-92 中表达时,犬 CD16A 和 CD64 均可诱导 ADCC。这些发现为工程化犬 NK 细胞或 T 细胞以表达高亲和力重组犬 CD64 铺平了道路,以最大限度地提高 ADCC,并测试它们的安全性和功效,以造福人类和犬类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c2/8907477/625c9fdaea54/fimmu-13-841859-g001.jpg

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