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免疫抑制酶IL4I1在人诱导的Aiolos+而非天然Helios+、FOXP3+调节性T细胞中的差异表达。

Differential expression of the immunosuppressive enzyme IL4I1 in human induced Aiolos+, but not natural Helios+, FOXP3+ Treg cells.

作者信息

Scarlata Clara-Maria, Celse Clotilde, Pignon Pascale, Ayyoub Maha, Valmori Danila

机构信息

Institut National de la Santé et de la Recherche Médicale, Unité 1102, Equipe Labellisée Ligue Contre le Cancer, Institut de Cancérologie de l'Ouest, Nantes-Saint Herblain, France.

出版信息

Eur J Immunol. 2015 Feb;45(2):474-9. doi: 10.1002/eji.201444897. Epub 2015 Jan 16.

Abstract

IL4I1 encodes an L-phenylalanine oxidase that inhibits T-cell proliferation. It has been recently reported that IL4I1 is expressed in TH17 cells as part of a mechanism that limits their pathogenicity. We have previously identified a population of human FOXP3(+) Treg cells that secrete IL-17 ex vivo; here, we addressed the expression of IL4I1 in that Treg-cell population. We found that in ex vivo isolated circulating Treg cells, IL4I1 expression is induced by activation. Moreover, IL4I1 expression is restricted to cells that do not express Helios, a transcription factor that characterizes natural Treg cells, but that express Aiolos, which is involved in the differentiation of TH17 and induced Treg cells. We also showed that conversion of Treg cells under inflammatory conditions increases IL4I1 expression, likely as part of a regulatory loop that attempts to limit the pathogenicity resulting from their conversion into TH17. The specific expression of IL4I1 in TH17 and iTreg cells may provide insights into approaches that aim at modulating these populations in different pathological conditions involving inflammation-mediated immunosuppression.

摘要

IL4I1编码一种抑制T细胞增殖的L-苯丙氨酸氧化酶。最近有报道称,IL4I1在TH17细胞中表达,作为限制其致病性机制的一部分。我们之前鉴定出一群在体外分泌IL-17的人FOXP3(+)调节性T细胞;在此,我们研究了IL4I1在该调节性T细胞群体中的表达。我们发现,在体外分离的循环调节性T细胞中,IL4I1的表达由激活诱导。此外,IL4I1的表达仅限于不表达Helios(一种表征天然调节性T细胞的转录因子)但表达Aiolos(参与TH17和诱导性调节性T细胞分化)的细胞。我们还表明,炎症条件下调节性T细胞的转化会增加IL4I1的表达,这可能是试图限制其转化为TH17所导致的致病性的调节回路的一部分。IL4I1在TH17和诱导性调节性T细胞中的特异性表达可能为旨在调节涉及炎症介导的免疫抑制的不同病理条件下这些细胞群体的方法提供见解。

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