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一种针对犬CD25的新型单克隆抗体(P4A10):犬调节性T细胞的筛选与评估

A novel monoclonal antibody specific for canine CD25 (P4A10): selection and evaluation of canine Tregs.

作者信息

Abrams V Kraig, Hwang Billanna, Lesnikova Marina, Gass M John, Wayner Elizabeth, Castilla-Llorente Cristina, Georges George E, Nash Richard A

机构信息

Fred Hutchinson Cancer Research Center, Seattle, WA 98109-102, United States.

出版信息

Vet Immunol Immunopathol. 2010 Jun 15;135(3-4):257-65. doi: 10.1016/j.vetimm.2009.12.006. Epub 2009 Dec 29.

Abstract

A monoclonal antibody (mAb), P4A10, was made to the canine interleukin-2 receptor alpha chain (IL-2Ralpha; p55; Tac antigen; CD25) to facilitate studies of canine regulatory T-cells (Treg). By non-reduced Western blot, P4A10 bound to a 55kDa protein, the size of human IL-2Ralpha. In flow cytometry assays, it reacted with a minor population of circulating dog CD3(+)CD4(+) T-cells and the majority (>60%) of in vitro PMA-Ionomycin (PMA-IO)-activated canine CD3(+) T-cells. P4A10 recognized a hematopoietic cell population enriched for FoxP3+ cells as measured by flow cytometry. The P4A10-selected fractions of T-cells had significantly increased copy numbers of CD25, FoxP3, IL-10, and TGFbeta as detected by RT-PCR (reverse transcriptase-PCR) compared to the negative fractions. The P4A10-selected cells inhibited (3)H (tritiated) thymidine incorporation in a mixed leukocyte reaction (MLR) containing responders of the same origin. P4A10-selected T-cells from fresh peripheral blood mononuclear cells had less FoxP3 (p=0.07) by qRT-PCR (quantitative RT-PCR) and were less suppressive (p=0.01) than in vitro alloantigen-activated Treg. The mAb P4A10 is specific for canine CD25 and can be used to facilitate studies of CD25+FoxP3+ Treg in this clinically relevant large animal model.

摘要

制备了一种针对犬白细胞介素-2受体α链(IL-2Rα;p55;Tac抗原;CD25)的单克隆抗体(mAb)P4A10,以促进对犬调节性T细胞(Treg)的研究。通过非还原Western印迹法,P4A10与一种55kDa的蛋白质结合,该蛋白质与人IL-2Rα的大小相同。在流式细胞术分析中,它与一小部分循环犬CD3(+)CD4(+) T细胞以及大多数(>60%)体外经佛波酯-离子霉素(PMA-IO)激活的犬CD3(+) T细胞发生反应。通过流式细胞术检测,P4A10识别出一个富含FoxP3+细胞的造血细胞群体。与阴性部分相比,经P4A10选择的T细胞部分通过逆转录聚合酶链反应(RT-PCR)检测到CD25、FoxP3、IL-10和转化生长因子β(TGFβ)的拷贝数显著增加。在含有同源应答细胞的混合淋巴细胞反应(MLR)中,经P4A10选择的细胞抑制了氚标记胸腺嘧啶核苷的掺入。通过定量逆转录聚合酶链反应(qRT-PCR)检测,来自新鲜外周血单个核细胞的经P4A10选择的T细胞的FoxP3含量较少(p = 0.07),且抑制作用比体外同种异体抗原激活的Treg弱(p = 0.01)。单克隆抗体P4A10对犬CD25具有特异性,可用于促进在这种临床相关的大型动物模型中对CD25+FoxP3+ Treg的研究。

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