[严重联合免疫缺陷,1999-2020年期间智利确诊患者的报告]。

Q3 Medicine Revista Chilena de Pediatria-Chile Pub Date : 2020-12-01 Epub Date: 2020-10-21 DOI:10.32641/rchped.vi91i6.2580
Rodrigo Hoyos-Bachiloglu, Jorge Rojas, Arturo Borzutzky, Pamela Hernández, Ana María Vinet, Paula Bustos, Fabiola Fernández, Macarena Lagos, Alexis Strickler, María Angélica Marinovic, Cristina Casado, María Cecilia Poli, Alejandra King
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SCID was diagnosed according to the cri teria proposed by Shearer: T lymphocytes (CD3+) < 300 cells/μL and proliferation 10% of the limit of normality in response to phytohemagglutinin or presence of T lymphocytes of maternal origin. Data collected from the clinical records were: sex, age at diagnosis, consanguinity, region of origin, lymphocyte subpopulations, genetic diagnosis, infectious and non-infectious complications, BCG vaccination and its complications, age at referral to the bone marrow transplant (BMT) center, and cause of non-BMT-related mortality. RESULTS Between 1999 and 2020, 25 patients were diagnosed with SCID. 78% of them were male, mean age at first manifestation of the disease was 2.3 months (0-7), while the mean age at diagnosis was 3.4 months (0-7). 16% of patients had a family history of SCID. 40% of cases were diagnosed within the Metropolitan Region. The most frequent immuno- phenotype was T-B-NK+ SCID (48%). 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引用次数: 0

摘要

重度联合免疫缺陷(SCID)是原发性免疫缺陷最严重的形式。迄今为止,关于这种疾病的当地信息很少。目的:了解智利SCID患者的流行病学、并发症、预后和卡介苗的使用情况。患者和方法:回顾性回顾1999年至2020年智利临床免疫学家诊断为SCID的患者的临床记录。根据Shearer提出的标准诊断SCID: T淋巴细胞(CD3+) < 300 cells/μL,对植物血凝素或母源T淋巴细胞的反应增殖正常限度的10%。从临床记录中收集的数据包括:性别、诊断年龄、血缘关系、原产地区、淋巴细胞亚群、遗传诊断、感染性和非感染性并发症、卡介苗接种及其并发症、转诊至骨髓移植(BMT)中心的年龄、非BMT相关死亡原因。结果:1999年至2020年间,25例患者被诊断为SCID。男性占78%,初发平均年龄2.3个月(0 ~ 7岁),确诊平均年龄3.4个月(0 ~ 7岁)。16%的患者有SCID家族史。40%的病例是在大都市区诊断出来的。最常见的免疫表型是T-B-NK+ SCID(48%)。69.5%的病例进行了遗传研究,RAG2基因突变是SCID最常见的病因(39%)。88%的SCID患者在诊断前接种过卡介苗(BCG),其中2例有已知的SCID家族史。接种疫苗的人中有36%出现了bcg相关并发症。转介至骨髓移植中心的平均年龄为7.4个月(5-16岁)。11/25的患者在被转移到移植中心之前死亡。讨论:智利患者的首次表现与SCID诊断之间存在显著的临床延迟,并且SCID诊断与转诊至BMT中心之间存在重要的时间间隔。智利的大多数SCID病例接受了卡介苗疫苗,尽管已知有该病的家族史,并经常出现疫苗相关并发症。
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[Severe combined immunodeficiency, report of chilean patients diagnosed during the 1999-2020 period].
INTRODUCTION Severe combined immunodeficiency (SCID) is the most severe form of primary immunodeficiency. To date, there is little local information about this disease. OBJECTIVE To describe the epidemiology, complications, prognosis, and use of the BCG vaccine in Chilean patients with SCID. PATIENTS AND METHOD Retrospective review of the clinical records of patients diagnosed with SCID by clinical immunologists between 1999 and 2020 throughout Chile. SCID was diagnosed according to the cri teria proposed by Shearer: T lymphocytes (CD3+) < 300 cells/μL and proliferation 10% of the limit of normality in response to phytohemagglutinin or presence of T lymphocytes of maternal origin. Data collected from the clinical records were: sex, age at diagnosis, consanguinity, region of origin, lymphocyte subpopulations, genetic diagnosis, infectious and non-infectious complications, BCG vaccination and its complications, age at referral to the bone marrow transplant (BMT) center, and cause of non-BMT-related mortality. RESULTS Between 1999 and 2020, 25 patients were diagnosed with SCID. 78% of them were male, mean age at first manifestation of the disease was 2.3 months (0-7), while the mean age at diagnosis was 3.4 months (0-7). 16% of patients had a family history of SCID. 40% of cases were diagnosed within the Metropolitan Region. The most frequent immuno- phenotype was T-B-NK+ SCID (48%). Genetic studies were done in 69.5% of cases, mutations in the RAG2 gene were the most common etiology of SCID (39%). 88% of SCID patients received the Bacillus Calmette-Guerin (BCG) vaccine before diagnosis, including 2 cases with a known family history of SCID. 36% of those who received the vaccine had BCG-related complications. The mean age at referral to a bone marrow transplant center was 7.4 months (5-16). 11/25 patients died before being transferred to a transplant center. DISCUSSION There is a clinically significant delay between the first manifestations and the diagnosis of SCID in Chilean patients, as well as an important time gap between the diagnosis of SCID and referral to a center for BMT. Most SCID cases in Chile receive the BCG vaccine, despite a known family history of the disease, and frequently develop vaccine-related complications.
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