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用唾液酸修饰的供体同种异体抗原靶向受体树突状细胞可延长皮肤移植存活时间。

Targeting Recipient Dendritic Cells with Sialic Acid-Modified Donor Alloantigen Prolongs Skin Transplant Survival.

作者信息

Sen Monica, Peng Qi, Ratnasothy Kulachelvy, Ambrosini Martino, Kalay Hakan, Bazoer Jordan, Adams Kate E, Ouazzani Nouhad El, Ababou Abdessamad, Guiliano David B, Saldaña Jose I, Kooyk Yvette van, Lombardi Giovanna, Smyth Lesley A

机构信息

School of Health, Sport and Bioscience, University of East London, Water Lane, London E15 4LZ, UK.

MRC Centre for Transplantation, Peter Gorer Department of Immunobiology, School of Immunology & Microbial Sciences, King's College London, London SE1 9RT, UK.

出版信息

Int J Mol Sci. 2025 Jun 26;26(13):6168. doi: 10.3390/ijms26136168.

Abstract

Mature dendritic cells (DCs) are known to activate effector immune responses, whereas steady state immature DCs can induce tolerance. Several studies have targeted immature murine quiescent DCs in vivo with antigen, including donor alloantigens, for the induction of tolerance. Receptors expressed by specific DC subsets have been also targeted with antibodies linked with antigens to induce tolerance; for instance, in vivo targeting of the DCIR2 DC subset with donor alloantigen resulted in long-term survival of heart and skin transplants. DCs also express sialic acid immunoglobulin-like lectin (Siglec) receptors, and these have been successfully targeted with myelin oligiodendrocyte glycoprotein (MOG) antigen to induce tolerance in experimental autoimmune encephalomyelitis (EAE). We investigated, in a mismatched model of skin transplant (B6K into B6 recipient mice), whether targeting a sialylated alloantigen K (Sia-K) to Siglecs on recipient DCs promoted transplant survival. The injection of α2,3 Sia-K into B6 recipient mice prior to B6K skin transplantation, by binding to Batf3 dependent DCs, resulted in prolonged skin graft survival and an increase in CD4CD62LFoxp3 Tregs. Targeting Siglecs on DC subsets in vivo represents a novel way of improving transplant survival.

摘要

已知成熟树突状细胞(DCs)可激活效应免疫反应,而稳态未成熟DCs可诱导免疫耐受。多项研究在体内用抗原(包括供体同种异体抗原)靶向未成熟的小鼠静止DCs,以诱导免疫耐受。特定DC亚群表达的受体也已被与抗原相连的抗体靶向,以诱导免疫耐受;例如,用供体同种异体抗原在体内靶向DCIR2 DC亚群可使心脏和皮肤移植长期存活。DCs还表达唾液酸免疫球蛋白样凝集素(Siglec)受体,这些受体已成功地被髓鞘少突胶质细胞糖蛋白(MOG)抗原靶向,以在实验性自身免疫性脑脊髓炎(EAE)中诱导免疫耐受。我们在皮肤移植不匹配模型(将B6K移植到B6受体小鼠中)中研究了将唾液酸化同种异体抗原K(Sia-K)靶向受体DCs上的Siglecs是否能促进移植存活。在进行B6K皮肤移植前,将α2,3 Sia-K注射到B6受体小鼠体内,通过与Batf3依赖性DCs结合,可延长皮肤移植物的存活时间,并增加CD4CD62LFoxp3调节性T细胞的数量。在体内靶向DC亚群上的Siglecs是提高移植存活率的一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97d6/12250551/1110332c1d97/ijms-26-06168-g001.jpg

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