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中国大陆 X 连锁淋巴组织增生症:临床、遗传和免疫学特征的综述。

X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic.

机构信息

Ministry of Education Key Laboratory of Child Development and Disorders, Children's Hospital of Chongqing Medical University, Chongqing, China.

Chongqing Key Laboratory of Child Infection and Immunity, Children's Hospital of Chongqing Medical University, Chongqing, China.

出版信息

Eur J Pediatr. 2020 Feb;179(2):327-338. doi: 10.1007/s00431-019-03512-7. Epub 2019 Nov 21.

DOI:10.1007/s00431-019-03512-7
PMID:31754776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6970958/
Abstract

X-linked lymphoproliferative syndrome (XLP) is a rare primary immunodeficiency disease that can be divided into two types: SAP deficiency (XLP1) and XIAP deficiency (XLP2), caused by mutations in the SH2D1A and XIAP genes, respectively. Few cases of XLP (particularly XIAP deficiency) have been reported in mainland China; hence, little is known about the characteristics of Chinese patients with XLP. We identified 13 and 7 patients with SAP and XIAP deficiency, respectively, in our center. Of our 20 patients, 19/20 (95%) presented with disease symptoms at a very early age: six in infancy and 13 in childhood. One XIAP- and three SAP-deficient patients died, while 3/7(42.9%) and 4/13(30.8%), respectively, developed hemophagocytic lymphohistiocytosis (HLH). Epstein-Barr virus (EBV) infection was significantly more common in SAP-deficient 10/13 (76.9%) than XIAP-deficient 2/7 (28.6%) patients, as was hypogammaglobulinemia (10/13 (76.9%) vs. 1/7 (14.3%)). None of the seven XIAP-deficient patients had colitis or lymphoma. Nine SAP-deficient patients and five XIAP-deficient patients showed markedly deficient SAP and XIAP expression, respectively, in lymphocytes. Significantly reduced levels of switched memory B cells were observed in six SAP-deficient patients with persistent hypogammaglobulinemia. One of 13 (7.7%) SAP-deficient patients and 1 of 7 (12.3%) XIAP-deficient patients have received HSCT treatment and are now alive and well; the other alive patients were waiting for HSCT. We also summarized clinical, genetic, and immunological characteristics of all 55 patients (including our 20 patients) reported in the literature in mainland China today.Conclusion: The overall characteristics of SAP deficiency in mainland China were consistent with those in previous reports, whereas manifestations of XIAP deficiency varied significantly. None of inflammatory bowel disease (IBD) has been reported among XIAP-deficient patients in our center; however, whether Chinese XIAP-deficient patients will develop colitis in the future warrants further investigation. HSCT is the only curative therapy for XLP and this therapy should be urgently considered.What is Known:• SAP and XIAP deficiencies share common clinical feature, HLH, whereas they also have their own specific manifestations.• IBD affects 25-30% of XIAP-deficient patients, which has been reported in other countries especially in European country and Japan.What is New:• This is the largest patient cohort study of XLP in China.• We firstly summarized the clinical features and outcomes of Chinese XIAP-deficient patients and found only 1 in 22 patients developed IBD and diet background may contribute to it; Asian SAP-deficient patients carrying SH2D1A R55X mutation were more prone to HLH.

摘要

X 连锁淋巴组织增生性疾病(XLP)是一种罕见的原发性免疫缺陷病,可分为 SAP 缺乏症(XLP1)和 XIAP 缺乏症(XLP2)两种类型,分别由 SH2D1A 和 XIAP 基因突变引起。中国内地报道的 XLP 病例(尤其是 XIAP 缺乏症)较少,因此,对于中国 XLP 患者的特征了解甚少。我们在中心分别鉴定出 13 例和 7 例 SAP 和 XIAP 缺乏症患者。在我们的 20 例患者中,19/20(95%)在非常年幼时出现疾病症状:6 例在婴儿期,13 例在儿童期。1 例 XIAP 缺乏症和 3 例 SAP 缺乏症患者死亡,而 3/7(42.9%)和 4/13(30.8%)分别发展为噬血细胞性淋巴组织细胞增生症(HLH)。EBV 感染在 13 例 SAP 缺乏症患者中明显更为常见(10/13,76.9%),而在 7 例 XIAP 缺乏症患者中则明显更为少见(2/7,28.6%),低丙种球蛋白血症也更为常见(10/13,76.9% vs. 1/7,14.3%)。7 例 XIAP 缺乏症患者均无结肠炎或淋巴瘤。9 例 SAP 缺乏症患者和 5 例 XIAP 缺乏症患者的淋巴细胞中分别明显缺乏 SAP 和 XIAP 表达。在 6 例持续低丙种球蛋白血症的 SAP 缺乏症患者中,观察到记忆 B 细胞的 switched 明显减少。在 13 例 SAP 缺乏症患者中有 1 例(7.7%)和在 7 例 XIAP 缺乏症患者中有 1 例(12.3%)接受了 HSCT 治疗,目前情况良好;其他存活患者正在等待 HSCT。我们还总结了目前中国大陆文献中报道的 55 例(包括我们的 20 例)患者的临床、遗传和免疫学特征。

结论

中国大陆 SAP 缺乏症的总体特征与以往报道一致,而 XIAP 缺乏症的表现则存在显著差异。我们中心尚未报告 XIAP 缺乏症患者出现炎症性肠病(IBD);然而,未来中国 XIAP 缺乏症患者是否会发展为结肠炎仍需要进一步研究。HSCT 是 XLP 的唯一治愈性治疗方法,应紧急考虑该治疗方法。

已知

  1. SAP 和 XIAP 缺乏症具有共同的临床特征 HLH,但它们也有自己的特定表现。

  2. IBD 影响 25-30%的 XIAP 缺乏症患者,这种情况在其他国家,特别是在欧洲国家和日本已有报道。

新发现

  1. 这是中国最大的 XLP 患者队列研究。

  2. 我们首次总结了中国 XIAP 缺乏症患者的临床特征和结局,发现只有 1/22 的患者发生了 IBD,饮食背景可能对此有影响;亚洲携带 SH2D1A R55X 突变的 SAP 缺乏症患者更易发生 HLH。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e95/6970958/af621713a4c0/431_2019_3512_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e95/6970958/af621713a4c0/431_2019_3512_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e95/6970958/af621713a4c0/431_2019_3512_Fig1_HTML.jpg

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