超越迷人:自身免疫淋巴增生性综合征和活化pi3k δ综合征的诊断和管理进展。

IF 2.9 3区 教育学 Q1 EDUCATION, SCIENTIFIC DISCIPLINES Hematology. American Society of Hematology. Education Program Pub Date : 2024-12-06 DOI:10.1182/hematology.2024000537
V Koneti Rao, Stefania Pittaluga, Gulbu Uzel
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引用次数: 0

摘要

难治性自身免疫性多系细胞减少症可出现于儿童期,伴有慢性非恶性淋巴增生(脾肿大、肝肿大和/或淋巴结病)。自20世纪50年代以来,由于外周破坏和隔离引起的细胞减少症已经得到了很好的认识,并且经常被合并为同名综合征,如Evans综合征和Canale-Smith综合征。尽管他们的临床和基因诊断检查看起来令人生畏,但它可以为早期干预、遗传咨询、经验和靶向治疗提供基础。自身免疫性淋巴细胞增生性综合征(ALPS)、活化磷脂酰肌醇3-激酶δ综合征(APDS)和许多其他相关遗传疾病统称为先天性免疫错误(IEI)。它们在儿童早期表现为顽固性自身免疫性细胞减少症,原因是免疫失调导致淋巴结病变、脾肿大和淋巴瘤易感性增加。最近,对照临床试验表明,一些具有血液学表现的免疫系统疾病可能更容易接受特定的靶向治疗,从而预防终末器官损伤和相关的合并症。在过去的20年里,雷帕霉素和霉酚酸酯已被成功地用作阿尔卑斯山的长期类固醇保护措施。目前APDS/PASLI(磷酸肌肽3-激酶[PI3K]相关的衰老T淋巴细胞,淋巴结病和免疫缺陷)的治疗选择包括口服生物可利用的PI3Kδ抑制剂lenolisib,该药物于2023年获得美国食品和药物管理局(FDA)的许可,用于12岁以上的个体作为靶向治疗。从罕见遗传疾病(如ALPS和APDS)患者身上学到的范例可能有助于探索和简化更广泛的以难治性细胞减少和淋巴细胞增生为表现的IEIs患者的分子治疗策略。
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Beyond FAScinating: advances in diagnosis and management of autoimmune lymphoproliferative syndrome and activated PI3 kinase δ syndrome.

Refractory autoimmune mutilineage cytopenias can present in childhood associated with chronic nonmalignant lymphoproliferation (splenomegaly, hepatomegaly, and/or lymphadenopathy). Cytopenias due to peripheral destruction and sequestration have been well recognized since the 1950s and are often lumped together as eponymous syndromes, such as Evans syndrome and Canale-Smith syndrome. Though their clinical and genetic diagnostic workup may appear daunting, it can provide the basis for early intervention, genetic counseling, and empirical and targeted therapies. Autoimmune lymphoproliferative syndrome (ALPS), activated phosphatidylinositol 3-kinase delta syndrome (APDS), and many other related genetic disorders are otherwise collectively known as inborn errors of immunity (IEI). They present in early childhood as refractory autoimmune cytopenias due to immune dysregulation leading to lymphadenopathy, splenomegaly, and increased susceptibility to lymphoma. More recently, controlled clinical trials have shown that some of these immune system disorders with hematological manifestations might be more readily amenable to specific targeted treatments, thus preventing end-organ damage and associated comorbidities. Over the last 20 years, both rapamycin and mycophenolate mofetil have been successfully used as steroid-sparing long-term measures in ALPS. Current therapeutic options for APDS/PASLI (phosphoinositide 3-kinase [PI3K]-associated senescent T lymphocytes, lymphadenopathy, and immunodeficiency) include the orally bioavailable PI3Kδ inhibitor, leniolisib, which was licensed by the US Food and Drug Administration (FDA) in 2023 for use in individuals older than 12 years as a targeted treatment. Paradigms learned from patients with rare genetic disorders like ALPS and APDS may help in exploring and streamlining molecular therapy strategies in the wider group of IEIs presenting with refractory cytopenias and lymphoproliferation.

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来源期刊
Hematology. American Society of Hematology. Education Program
Hematology. American Society of Hematology. Education Program EDUCATION, SCIENTIFIC DISCIPLINES-HEMATOLOGY
CiteScore
4.70
自引率
3.30%
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0
期刊介绍: Hematology, the ASH Education Program, is published annually by the American Society of Hematology (ASH) in one volume per year.
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