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Guidelines for assessing immunocompetency in clinical trials for autoimmune diseases

机译:自身免疫性疾病临床试验中评估免疫能力的指南

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摘要

Clinical trials testing the safety and efficacy of immunosuppressive agents for the treatment of autoimmune diseases should also be designed to evaluate immunocompetency. The most clinically relevant outcome for assessing immunocompetency is the infection rate. Therefore, a systematic approach to screening, monitoring, and reporting infections, modeled after the recommendations of the American Society of Transplantation, is presented. However, because the baseline infection rate in most autoimmune diseases is low, additional tests for immunocompetency should be considered. Evaluation of vaccine responses, an alternative clinically relevant approach, may be particularly useful. Other adjunctive approaches to evaluation of immunocompetency are discussed including immunization with non-vaccine neoantigens, surveillance of chronic viral infections, in vivo or in vitro assessment of cellular immunity, and analysis of innate immunity. Banking genetic material to allow genotyping should be considered particularly if a central repository for samples from different trials can be established.
机译:还应该设计用于测试免疫抑制剂治疗自身免疫性疾病的安全性和有效性的临床试验,以评估免疫能力。评估免疫能力最临床相关的结果是感染率。因此,提出了一种以美国移植学会的建议为蓝本的系统化方法,用于筛查,监测和报告感染。但是,由于大多数自身免疫性疾病的基线感染率较低,因此应考虑进行其他免疫能力测试。评估疫苗反应(一种替代的临床相关方法)可能特别有用。讨论了其他评估免疫能力的辅助方法,包括用非疫苗新抗原进行免疫,监测慢性病毒感染,体内或体外细胞免疫评估以及先天免疫分析。特别是如果可以建立来自不同试验的样品的中央储存库,则应考虑将基因材料保存起来以进行基因分型。

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