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同种异体Tregs在失能后扩增,在炎症条件下仍具有抑制作用,但缺乏肠道归巢分子的表达。

Allospecific Tregs Expanded After Anergization Remain Suppressive in Inflammatory Conditions but Lack Expression of Gut-homing Molecules.

作者信息

Kotsiou Eleni, Gribben John G, Davies Jeff K

机构信息

Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University London, London, UK.

Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University London, London, UK.

出版信息

Mol Ther. 2016 Jun;24(6):1126-1134. doi: 10.1038/mt.2016.64. Epub 2016 Apr 6.

Abstract

Cell therapy with antigen-specific regulatory T-cells (Treg) has great potential to selectively control unwanted immune responses after allogeneic stem-cell or solid organ transplantation and in autoimmune diseases. Ex vivo allostimulation with costimulatory blockade (alloanergization) of human T-cells expands populations of alloantigen-specific Treg, providing a cellular strategy to control donor T-cell alloresponses causing graft-versus-host disease after allogeneic hematopoietic stem-cell transplantation. Crucially, it is not known if Treg expanded in this way are stable in proinflammatory conditions encountered after transplantation, or if they possess capacity to migrate to key target organs. Using an in vitro model to functionally characterize human Treg expanded after alloanergization, we now show that these cells remain potently allosuppressive in the presence of relevant exogenous inflammatory signals. Expanded allospecific Treg retained expression of molecules conferring migratory capacity to several organs but small intestine-specific chemotaxis was markedly impaired, in keeping with the preponderance of gut graft-versus-host disease in previous clinical studies using this strategy. Importantly, impaired gut-specific chemotaxis could be partially corrected by pharmacological treatment. These findings will facilitate more effective application of this cellular approach to limit T-cell alloresponses after hematopoietic stem-cell transplantation and the wider application of the strategy to other clinical settings.

摘要

用抗原特异性调节性T细胞(Treg)进行细胞治疗在选择性控制异基因干细胞或实体器官移植后以及自身免疫性疾病中的有害免疫反应方面具有巨大潜力。对人T细胞进行共刺激阻断的体外同种异体刺激(同种异体失能)可扩大同种异体抗原特异性Treg群体,为控制异基因造血干细胞移植后引起移植物抗宿主病的供体T细胞同种异体反应提供了一种细胞策略。至关重要的是,目前尚不清楚以这种方式扩增的Treg在移植后遇到的促炎条件下是否稳定,或者它们是否具有迁移到关键靶器官的能力。我们使用体外模型对同种异体失能后扩增的人Treg进行功能表征,现在表明这些细胞在存在相关外源性炎症信号的情况下仍具有强大的同种异体抑制作用。扩增的同种特异性Treg保留了赋予向多个器官迁移能力的分子表达,但小肠特异性趋化性明显受损,这与之前使用该策略的临床研究中肠道移植物抗宿主病的优势一致。重要的是,肠道特异性趋化性受损可通过药物治疗得到部分纠正。这些发现将有助于更有效地应用这种细胞方法来限制造血干细胞移植后的T细胞同种异体反应,并将该策略更广泛地应用于其他临床环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8183/4923329/9f59d99c7ff5/mt201664f1.jpg

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