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在HLA - DRB1*04、DQ8 1型糖尿病中,自身免疫性T细胞针对前胰岛素原产生的促炎和抗炎细胞因子。

Pro- and anti-inflammatory cytokine production by autoimmune T cells against preproinsulin in HLA-DRB1*04, DQ8 Type 1 diabetes.

作者信息

Durinovic-Belló I, Schlosser M, Riedl M, Maisel N, Rosinger S, Kalbacher H, Deeg M, Ziegler M, Elliott J, Roep B O, Karges W, Boehm B O

机构信息

Department of Internal Medicine I, Division of Endocrinology, University of Ulm, Robert-Koch Str. 8, 89081, Ulm, Germany.

Institute of Pathophysiology Karlsburg, University of Greifswald, Greifswald, Germany.

出版信息

Diabetologia. 2004 Mar;47(3):439-450. doi: 10.1007/s00125-003-1315-1. Epub 2004 Jan 24.

Abstract

AIMS/HYPOTHESIS: Preproinsulin is a target T cell autoantigen in human Type 1 diabetes. This study analyses the phenotype and epitope recognition of preproinsulin reactive T cells in subjects with a high genetic risk of diabetes [HLA-DRB1*04, DQ8 with Ab+ (autoantibody-positive) or without islet autoantibodies (control subjects)], and in HLA-matched diabetic patients.

METHODS

A preproinsulin peptide library approach was used to screen for cytokine profiles and epitope specificities in human peripheral blood lymphocytes, and CD4(+)CD45RA(-) and CD4(+)CD45RA(+) T cell subfractions, representing memory and naive and recently primed T cells respectively.

RESULTS

In CD4(+) T cell subsets we identified immunodominant epitopes and cytokine production patterns that differed profoundly between patients, Ab+ subjects and non-diabetic HLA-matched control subjects. In Ab+ subjects, a C-peptide epitope C13-29 and insulin B-chain epitope B11-27 were preferentially recognised, whereas insulin-treated Type 1 diabetic patients reacted to native insulin and B-chain epitope B1-16. In peripheral blood lymphocytes of Ab+ subjects, an increase in T helper (Th) 1 (IFNgamma, IL-2) and Th2 (IL-4) cytokines was detectable, wheras in CD45RA(+) and CD45RA(-) subsets, IL-4 and IL-10 phenotypes dominated, compatible with the contribution of non-CD4 cells to IFNgamma content. In insulin-treated Type 1 diabetic patients, naive and recently primed CD4(+) cells were characterised by increasd IFNgamma, TNFalpha, and IL-5.

CONCLUSIONS/INTERPRETATION: Our data show that T cell reactivity to preproinsulin in CD45RA subsets is Th2-dominant in Ab+ subjects, challenging the Th1 paradigm in Type 1 diabetes. Characteristic immunodominant epitopes and cytokine patterns distinguish diabetic patients and Ab+ subjects from HLA-matched healthy individuals. This could prove useful in monitoring of T-cell immunity in clinical diabetes intervention trials.

摘要

目的/假设:前胰岛素原是人类1型糖尿病中的一种靶标T细胞自身抗原。本研究分析了糖尿病遗传风险高的受试者[携带HLA - DRB1*04、DQ8且抗体阳性(自身抗体阳性)或无胰岛自身抗体(对照受试者)]以及HLA匹配的糖尿病患者中前胰岛素原反应性T细胞的表型和表位识别情况。

方法

采用前胰岛素原肽库方法筛选人外周血淋巴细胞以及分别代表记忆性、初始和近期致敏T细胞的CD4(+)CD45RA(-)和CD4(+)CD45RA(+) T细胞亚群中的细胞因子谱和表位特异性。

结果

在CD4(+) T细胞亚群中,我们鉴定出患者、抗体阳性受试者和非糖尿病HLA匹配对照受试者之间免疫显性表位和细胞因子产生模式存在显著差异。在抗体阳性受试者中,优先识别C肽表位C13 - 29和胰岛素B链表位B11 - 27,而胰岛素治疗的1型糖尿病患者对天然胰岛素和B链表位B1 - 16有反应。在抗体阳性受试者的外周血淋巴细胞中,可检测到辅助性T细胞(Th)1(IFNγ、IL - 2)和Th2(IL - 4)细胞因子增加,而在CD45RA(+)和CD45RA(-)亚群中,IL - 4和IL - 10表型占主导,这与非CD4细胞对IFNγ含量的贡献一致。在胰岛素治疗的1型糖尿病患者中,初始和近期致敏的CD4(+)细胞的特征是IFNγ、TNFα和IL - 5增加。

结论/解读:我们的数据表明,在抗体阳性受试者中,CD45RA亚群中对前胰岛素原的T细胞反应以Th2为主导,这对1型糖尿病中的Th1范式提出了挑战。特征性的免疫显性表位和细胞因子模式将糖尿病患者和抗体阳性受试者与HLA匹配的健康个体区分开来。这在临床糖尿病干预试验中监测T细胞免疫方面可能会有帮助。

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