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在不依赖B细胞受体摄取木瓜蛋白酶后,B细胞调节CD4 + T细胞对木瓜蛋白酶的反应。

B cells regulate CD4+ T cell responses to papain following B cell receptor-independent papain uptake.

作者信息

Dwyer Daniel F, Woodruff Matthew C, Carroll Michael C, Austen K Frank, Gurish Michael F

机构信息

Division of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115; and.

Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.

出版信息

J Immunol. 2014 Jul 15;193(2):529-39. doi: 10.4049/jimmunol.1303247. Epub 2014 Jun 13.

Abstract

Papain, a cysteine protease allergen with inherent adjuvant activity, induces potent IL-4 expression by T cells in the popliteal lymph nodes of mice following footpad immunization. In this study, we identify a novel, non-BCR-mediated capacity for B cells to rapidly bind and internalize papain. B cells subsequently regulate the adaptive immune response by enhancing ICOS expression on CD4(+) T cells and amplifying Th2 and follicular helper T cell induction. Ab blockade of ICOS ligand, expressed by popliteal lymph node B cells, but not dendritic cells, at the peak of the response inhibits IL-4 responses in wild-type mice but not B cell-deficient mice. Thus, B cells play a critical role in amplifying adjuvant-dependent Th2 polarization following noncanonical acquisition and internalization of the cysteine protease papain.

摘要

木瓜蛋白酶是一种具有固有佐剂活性的半胱氨酸蛋白酶变应原,在小鼠足垫免疫后,可诱导腘窝淋巴结中的T细胞强力表达白细胞介素-4(IL-4)。在本研究中,我们发现B细胞具有一种新的、非BCR介导的能力,可快速结合并内化木瓜蛋白酶。随后,B细胞通过增强CD4(+) T细胞上ICOS的表达以及放大Th2和滤泡辅助性T细胞的诱导来调节适应性免疫反应。在反应高峰期,阻断由腘窝淋巴结B细胞而非树突状细胞表达的ICOS配体的抗体,可抑制野生型小鼠的IL-4反应,但对B细胞缺陷型小鼠无效。因此,在非经典摄取和内化半胱氨酸蛋白酶木瓜蛋白酶后,B细胞在放大佐剂依赖性Th2极化过程中起关键作用。

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