阿他贝司他元特异性人类 T 细胞的选择性 HLA II 类等位基因限制性活化。

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL Chemical Research in Toxicology Pub Date : 2024-10-21 Epub Date: 2024-09-30 DOI:10.1021/acs.chemrestox.4c00262
Megan Ford, Paul J Thomson, Jan Snoeys, Xiaoli Meng, Dean J Naisbitt
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引用次数: 0

摘要

在接触过阿尔茨海默氏症药物阿他贝司他的几名试验患者中检测到肝酶升高,导致药物开发计划终止。对患者血液中的肝T淋巴细胞浸润和二氨基噻嗪(DIAT)代谢物反应性、人类白细胞抗原(HLA)-DR限制性、CD4+T淋巴细胞的特征描述证实了免疫发病机制。免疫介导的肝损伤患者表达了一组受限的 HLA-DRB1 等位基因,包括 HLA-DRB1*12:01、HLA-DRB1*13:02 和 HLA-DRB1*15:01。因此,本研究的目的是:(i) 从 HLA 基因分型的无药物依赖性供体中产生 DIAT 反应性 T 细胞克隆;(ii) 描述 DIAT 特异性 T 细胞激活的途径;(iii) 评估 DIAT 特异性 T 细胞反应的 HLA 等位基因限制。我们招募了 16 名表达上述 HLA-DR 分子的无毒供体,并生成了 T 细胞克隆。细胞表型、功能和 HLA-等位基因限制通过培养试验进行评估。质谱法分析了阿他贝司他存在和不存在时 HLA II 类分子显示的肽。从表达 HLA-DRB1*12:01、HLA-DRB1*13:02 和 HLA-DRB1*15:01 的供体中成功生成了几个对母体药物无反应的 DIAT 反应型 CD4+ 克隆,但从表达其他 HLA-DRB1 等位基因的供体中却没有生成。DIAT 与抗原呈递细胞表面表达的 HLA-DR 蛋白直接结合后,T 细胞克隆被激活。DIAT的结合并没有改变HLA-DRB1多肽的结合谱系,这表明这种结合是与HLA相关多肽而不是与HLA蛋白本身的结合相互作用。DIAT 特异性 T 细胞反应显示出 HLA-DRB1*12:01、HLA-DRB1*13:02 和 HLA-DRB1*15:01 限制。这些数据表明,DIAT 对 HLA 蛋白和相关肽具有一定程度的选择性,某些等位基因的表达会增加,而其他等位基因的表达则会减少,这样就有可能产生药物特异性 T 细胞反应。
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Selective HLA Class II Allele-Restricted Activation of Atabecestat Metabolite-Specific Human T-Cells.

Elevations in hepatic enzymes were detected in several trial patients exposed to the Alzheimer's drug atabecestat, which resulted in termination of the drug development program. Characterization of hepatic T-lymphocyte infiltrates and diaminothiazine (DIAT) metabolite-responsive, human leukocyte antigen (HLA)-DR-restricted, CD4+ T-lymphocytes in the blood of patients confirmed an immune pathogenesis. Patients with immune-mediated liver injury expressed a restricted panel of HLA-DRB1 alleles including HLA-DRB1*12:01, HLA-DRB1*13:02, and HLA-DRB1*15:01. Thus, the objectives of this study were to (i) generate DIAT-responsive T-cell clones from HLA-genotyped drug-naive donors, (ii) characterize pathways of DIAT-specific T-cell activation, and (iii) assess HLA allele restriction of the DIAT-specific T-cell response. Sixteen drug-naive donors expressing the HLA-DR molecules outlined above were recruited, and T-cell clones were generated. Cellular phenotype, function, and HLA-allele restriction were assessed using culture assays. Peptides displayed by HLA class II molecules in the presence and absence of atabecestat were analyzed by mass spectrometry. Several DIAT-responsive CD4+ clones, displaying no reactivity toward the parent drug, were successfully generated from donors expressing HLA-DRB1*12:01, HLA-DRB1*13:02, and HLA-DRB1*15:01 but not from other donors expressing other HLA-DRB1 alleles. T-cell clones were activated following direct binding of DIAT to HLA-DR proteins expressed on the surface of antigen presenting cells. DIAT binding did not alter the HLA-DRB1 peptide binding repertoire, indicative of a binding interaction with the HLA-associated peptide rather than with the HLA protein itself. DIAT-specific T-cell responses displayed HLA-DRB1*12:01, HLA-DRB1*13:02, and HLA-DRB1*15:01 restriction. These data demonstrate that DIAT displays a degree of selectivity toward HLA protein and associated peptides, with expression of certain alleles increasing and that of others decreasing, the likelihood that a drug-specific T-cell response develops.

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来源期刊
CiteScore
7.90
自引率
7.30%
发文量
215
审稿时长
3.5 months
期刊介绍: Chemical Research in Toxicology publishes Articles, Rapid Reports, Chemical Profiles, Reviews, Perspectives, Letters to the Editor, and ToxWatch on a wide range of topics in Toxicology that inform a chemical and molecular understanding and capacity to predict biological outcomes on the basis of structures and processes. The overarching goal of activities reported in the Journal are to provide knowledge and innovative approaches needed to promote intelligent solutions for human safety and ecosystem preservation. The journal emphasizes insight concerning mechanisms of toxicity over phenomenological observations. It upholds rigorous chemical, physical and mathematical standards for characterization and application of modern techniques.
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