Targeted treatments for immune dysregulation in inborn errors of immunity

N. Makkoukdji, Valishti Pundit, M. Wyke, Jheison Giraldo, Travis Satnarine, Gary I. Kleiner, Melissa Gans
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Abstract

Primary immune regulatory disorders (PIRDs) constitute a subset of inborn errors of immunity and are characterized by lymphoproliferation, autoimmunity, malignancy, and infection. Unlike classical primary immune deficiencies, initial symptoms of PIRDs can manifest as autoimmunity such as cytopenias or enteropathy, which can often prove resistant to conventional treatments and occur years prior to the onset of infectious complications. Raising awareness about PIRDs among specialists and adopting a multidisciplinary approach is crucial for early diagnosis, intervention, and potential prevention of severe organ damage. Significant progress has been made in identifying several PIRDs, which has contributed to a more comprehensive comprehension of their underlying immunological mechanisms. This knowledge has paved the way for targeted therapies focusing on specific molecules, which tend to offer superior disease control compared to traditional immunosuppressants. This review, informed by the latest literature, explores prevalent PIRDs, detailing their clinical manifestations and recent advancements in treatment modalities.
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先天性免疫错误中免疫失调的靶向治疗
原发性免疫调节紊乱(PIRDs)是先天性免疫错误的一个分支,其特点是淋巴细胞增殖、自身免疫、恶性肿瘤和感染。与传统的原发性免疫缺陷不同,PIRD 的初期症状可表现为细胞减少症或肠病等自身免疫症状,这些症状通常会对常规治疗产生抗药性,并在感染性并发症发生前数年出现。提高专科医生对 PIRD 的认识并采用多学科方法对于早期诊断、干预和预防严重器官损伤至关重要。在确定几种 PIRD 方面已经取得了重大进展,这有助于更全面地了解其潜在的免疫机制。这些知识为针对特定分子的靶向治疗铺平了道路,与传统的免疫抑制剂相比,靶向治疗往往能提供更好的疾病控制效果。本综述以最新文献为基础,探讨了流行的 PIRD,详细介绍了它们的临床表现和治疗方法的最新进展。
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