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抗 CD45RB/抗 TIM-1 诱导的耐受需要调节性 B 细胞。

Anti-CD45RB/anti-TIM-1-induced tolerance requires regulatory B cells.

机构信息

Division of Transplantation, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Am J Transplant. 2012 Aug;12(8):2072-8. doi: 10.1111/j.1600-6143.2012.04055.x. Epub 2012 Apr 11.

DOI:10.1111/j.1600-6143.2012.04055.x
PMID:22494812
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3396747/
Abstract

The role of B cells in transplant tolerance remains unclear. Although B-cell depletion often prolongs graft survival, sometimes it results in more rapid rejection, suggesting that B cells may have regulatory activity. We previously demonstrated that tolerance induction by anti-CD45RB antibody requires recipient B cells. Here, we show that anti-CD45RB in combination with anti-TIM-1 antibody has a synergistic effect, inducing tolerance in all recipients in a mouse islet allograft model. This effect depends on the presence of recipient B cells, requires B-cell IL-10 activity, and is antigen-specific. These data suggest the existence of a regulatory B-cell population that promotes tolerance via an IL-10-dependent pathway.

摘要

B 细胞在移植耐受中的作用尚不清楚。虽然 B 细胞耗竭通常会延长移植物的存活时间,但有时也会导致更快的排斥反应,这表明 B 细胞可能具有调节活性。我们之前的研究表明,抗 CD45RB 抗体诱导的耐受需要受体 B 细胞。在这里,我们显示抗 CD45RB 联合抗 TIM-1 抗体具有协同作用,在小鼠胰岛移植模型中诱导所有受体的耐受。这种作用依赖于受体 B 细胞的存在,需要 B 细胞 IL-10 活性,并且具有抗原特异性。这些数据表明存在一种调节性 B 细胞群体,通过 IL-10 依赖途径促进耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/025b064ffb14/nihms362879f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/87318d454c59/nihms362879f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/23385046ecdf/nihms362879f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/0ad718ab71c6/nihms362879f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/fd0a0f00c697/nihms362879f5a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/025b064ffb14/nihms362879f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/87318d454c59/nihms362879f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/a3ee8bb002ba/nihms362879f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/23385046ecdf/nihms362879f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/0ad718ab71c6/nihms362879f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/fd0a0f00c697/nihms362879f5a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb7/3396747/025b064ffb14/nihms362879f6.jpg

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2
TIM genes: a family of cell surface phosphatidylserine receptors that regulate innate and adaptive immunity.TIM 基因:一族细胞表面磷脂酰丝氨酸受体,调节固有免疫和适应性免疫。
Immunol Rev. 2010 May;235(1):172-89. doi: 10.1111/j.0105-2896.2010.00903.x.
3
Preemptive CD20+ B cell depletion attenuates cardiac allograft vasculopathy in cyclosporine-treated monkeys.
TIM-1在肿瘤发生发展及治疗中的作用。
Front Cell Dev Biol. 2024 May 20;12:1307806. doi: 10.3389/fcell.2024.1307806. eCollection 2024.
4
Cellular strategies to induce immune tolerance after liver transplantation: Clinical perspectives.肝移植后诱导免疫耐受的细胞策略:临床展望
World J Gastroenterol. 2024 Apr 7;30(13):1791-1800. doi: 10.3748/wjg.v30.i13.1791.
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Advances in the study of B cells in renal ischemia-reperfusion injury.肾缺血再灌注损伤中 B 细胞研究进展。
Front Immunol. 2023 Nov 1;14:1216094. doi: 10.3389/fimmu.2023.1216094. eCollection 2023.
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