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在小鼠中诱导适应性调节性T细胞的新型Treg表位

New tregitopes inducing adaptive regulatory T cells in mice.

作者信息

Okoniewska K M, Kedzierska A E, Okoniewski J, Slawek A, Grzymajlo K, Chelmonska-Soyta A, Grabowski T

机构信息

P.F.O. Vetos-Farma sp. z o.o., Bielawa, Poland.

Department of Clinical Pharmacology, Wroclaw Medical University, Wroclaw, Poland.

出版信息

J Physiol Pharmacol. 2017 Dec;68(6):897-906.

Abstract

Epitopes of regulatory T cells (tregitopes) represent linear sequences of amino acids that induce CD4CD25Foxp3 T lymphocytes expansion both in vitro and in vivo. The tregitopes' effectiveness was confirmed in autoimmune disease mouse models and in murine transplant models. Therefore, tregitopes together with regulatory T cells (Tregs) could play a major role in maintaining immune tolerance. The purpose of the presented study was a selection of potential tregitopes and assessment of their impact on Tregs expansion. Eight peptides were selected based on the previously published in silico model and their immunotolerogenic functions. To verify, if selected peptides are potential TCR ligands, the affinity of selected peptides to overrepresented in patients with autoimmune diseases, HLA-DRB1*04:01 allele, was measured by surface plasmon resonance. In order to evaluate the impact of potential tregitopes on the induction of Tregs in in vitro conditions, C57BL6Foxp3 mouse antigen presenting cells were co-cultured with naive syngeneic T cells under stimulation of selected peptides. CD4CD25Foxp3 and CD4CD25Foxp3IL-10 cells frequency was analyzed using flow cytometry. Based on Tregs induction, two tregitopes derived from yeast and adenovirus protein were identified. In summary, the performed studies allowed an identification of novel putative tregitopes, which application potential includes their use as immunomodulators in mice.

摘要

调节性T细胞表位(tregitopes)代表氨基酸的线性序列,可在体外和体内诱导CD4CD25Foxp3 T淋巴细胞扩增。tregitopes的有效性已在自身免疫性疾病小鼠模型和小鼠移植模型中得到证实。因此,tregitopes与调节性T细胞(Tregs)共同在维持免疫耐受中发挥重要作用。本研究的目的是筛选潜在的tregitopes并评估它们对Tregs扩增的影响。基于先前发表的计算机模拟模型及其免疫耐受功能,选择了8种肽。为了验证所选肽是否为潜在的TCR配体,通过表面等离子体共振测量了所选肽与自身免疫性疾病患者中高表达的HLA-DRB1*04:01等位基因的亲和力。为了评估潜在tregitopes在体外条件下对Tregs诱导的影响,在所选肽的刺激下,将C57BL6Foxp3小鼠抗原呈递细胞与同基因幼稚T细胞共培养。使用流式细胞术分析CD4CD25Foxp3和CD4CD25Foxp3IL-10细胞频率。基于Tregs诱导,鉴定出两种源自酵母和腺病毒蛋白的tregitopes。总之,所进行的研究使得能够鉴定出新的假定tregitopes,其应用潜力包括用作小鼠中的免疫调节剂。

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