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晚期胎儿胸腺切除术并不能预防出生后肠道归巢T细胞的发育。

Late-term fetal thymectomy does not prevent the development of gut-homing T cells after birth.

作者信息

Cahill R N, Kimpton W G, Washington E A, Dudler L, Trnka Z

机构信息

Laboratory for Foetal and Neonatal Immunology, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Immunology. 1996 May;88(1):130-3. doi: 10.1046/j.1365-2567.1996.d01-642.x.

Abstract

Tissue-specific circulation of T cells is a critical element in the integration of systemic immune responses. Current models of T-cell migration suggest that homing specificities of T cells for tissues such as gut and skin are generated outside the thymus as a result of activation of virgin T cells by antigen in lymph nodes. We have used the sheep fetus (which is immunologically virgin and contains no memory or effector T-cell subsets) to examine the migration of 51Cr-labelled T cells in vivo. We report that gut-homing T cells are not present in the fetus and that gut-homing T cells from postnatal lambs home normally to fetal gut. Fetal thymectomy performed immediately prior to birth failed to prevent the development of gut-homing T cells in postnatal life. Gut-homing specificities on T cells are thus acquired extrathymically.

摘要

T细胞的组织特异性循环是全身免疫反应整合中的关键要素。当前的T细胞迁移模型表明,T细胞对肠道和皮肤等组织的归巢特异性是在胸腺外产生的,这是由于原始T细胞在淋巴结中被抗原激活所致。我们利用绵羊胎儿(其在免疫上处于原始状态,不包含记忆或效应T细胞亚群)来检测体内51Cr标记的T细胞的迁移。我们报告称,胎儿中不存在肠道归巢T细胞,并且出生后羔羊的肠道归巢T细胞能正常归巢至胎儿肠道。出生前立即进行的胎儿胸腺切除术未能阻止出生后肠道归巢T细胞的发育。因此,T细胞上的肠道归巢特异性是在胸腺外获得的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c17/1456470/08db01d71909/immunology00032-0139-a.jpg

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