BASTA, a simple whole-blood assay for measuring β cell antigen–specific CD4 + T cell responses in type 1 diabetes

抗原 糖尿病 1型糖尿病 细胞 全血 2型糖尿病 免疫学 分子生物学 医学 生物 化学 生物化学 内分泌学
作者
Matthew Lacorcia,Pushpak Bhattacharjee,Abby Foster,Melinda Y. Hardy,Jason A. Tye‐Din,John A. Karas,John M. Wentworth,Fergus Cameron,Stuart I. Mannering
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science]
卷期号:17 (790): eadt2124-eadt2124 被引量:2
标识
DOI:10.1126/scitranslmed.adt2124
摘要

Type 1 diabetes (T1D) is an autoimmune disease where T cells mediate the destruction of the insulin-producing β cells found within the islets of Langerhans in the pancreas. Autoantibodies to β cell antigens are the only tests available to detect β cell autoimmunity. T cell responses to β cell antigens, which are known to cause T1D, can only be measured in research settings because of the complexity of assays and the large blood volumes required. Here, we describe the β cell antigen–specific T cell assay (BASTA). BASTA is a simple whole-blood assay that can detect human CD4 + T cell responses to β cell antigens by measuring antigen-stimulated interleukin-2 (IL-2) production. BASTA is both more sensitive and specific than the CFSE (carboxyfluorescein diacetate succinimidyl ester)–based proliferation assay. We used BASTA to identify the regions of preproinsulin that stimulated T cell responses specifically in blood from people with T1D. BASTA can be done with as little as 2 to 3 milliliters of blood. We found that effector memory CD4 + T cells are the primary producers of IL-2 in response to preproinsulin peptides. We then evaluated responses to individual and pooled preproinsulin peptides in a cross-sectional study of pediatric patients: without T1D, without T1D but with a first-degree relative with T1D, or diagnosed with T1D. In contrast with other preproinsulin peptides, full-length C-peptide (PI 33–63 ) showed high specificity for T1D [area under the curve (AUC) = 0.86)]. We suggest that BASTA will be a useful tool for monitoring changes in β cell–specific CD4 + T cell responses both in research and clinical settings.
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