Evaluation of immunological abnormalities in patients with rare syndromes.

IF 1.5 4区 医学 Q4 IMMUNOLOGY
Yahya Gul, Hasan Kapaklı, Selma Erol Aytekin, Şukru Nail Guner, Sevgi Keles, Ayşe Gül Zamani, Mahmut Selman Yıldırım, Ïsmail Reisli
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引用次数: 0

Abstract

Introduction: Recurrent infections are important problems in syndromic patients. This study aimed to evaluate immunological abnormalities in patients who presented with recurrent infections and were diagnosed with rare syndromes.

Material and methods: This retrospective analysis included 14 patients with complaints of recurrent infections, all of whom were diagnosed with a rare syndrome.

Results: The study group consisted of patients with Aicardi syndrome, Brugada syndrome, Phelan- McDermid syndrome, trichothiodystrophy, LEOPARD syndrome, Prader-Willi syndrome, Seckel syndrome, trisomy 18 (Edwards' syndrome), Wiedemann-Steiner syndrome, West syndrome, Williams syndrome, 47,XYY syndrome, 16p13 deletion syndrome, and 13q1.3 deletion syndrome. Seven patients (50%) were girls and seven (50%) were boys (mean age, 56.7 ±32.9 months; median [range] age: 45.5 [27-153] months). There were high rates of consanguinity (50%), cesarean section delivery (71%), and hospitalization in the intensive care unit (78.5%). No patients had a family history of immunodeficiency. On admission, all patients exhibited humoral and/or cellular immune system abnormalities. During the follow-up period, all T-cell abnormalities were improved after immunoglobulin replacement therapy (IGRT), while B-cell abnormalities persisted. These findings suggested that the patients predominantly had antibody deficiencies associated with mild T-cell abnormalities because of recurrent infections. The rates of infections and hospitalizations were significantly reduced after IGRT (p < 0.001); the rate of intensive care unit admission also significantly decreased (from 78.5% to 21.4%). Two of the three oxygen-dependent patients exhibited improvement therein. IGRT was discontinued in two patients with significant clinical improvement during follow-up.

Conclusions: An immunological evaluation should be considered in pediatric patients with rare syndromes and recurrent infections. IGRT may help to improve the prognoses of these patients.

罕见综合征患者免疫异常的评价。
反复感染是综合征患者的重要问题。本研究旨在评估出现复发性感染并被诊断为罕见综合征的患者的免疫异常。材料和方法:本回顾性分析包括14例复发性感染的患者,所有患者均被诊断为一种罕见综合征。结果:研究组包括Aicardi综合征、Brugada综合征、Phelan- McDermid综合征、毛甲状腺营养不良症、LEOPARD综合征、Prader-Willi综合征、Seckel综合征、18三体(Edwards综合征)、Wiedemann-Steiner综合征、West综合征、Williams综合征、47、XYY综合征、16p13缺失综合征、13q1.3缺失综合征患者。女孩7例(50%),男孩7例(50%),平均年龄56.7±32.9个月;中位年龄:45.5[27-153]个月)。血亲率高(50%),剖宫产率高(71%),重症监护病房住院率高(78.5%)。没有患者有免疫缺陷家族史。入院时,所有患者均表现出体液和/或细胞免疫系统异常。在随访期间,免疫球蛋白替代治疗(IGRT)后,所有t细胞异常均得到改善,而b细胞异常持续存在。这些发现表明,由于复发性感染,患者主要存在与轻度t细胞异常相关的抗体缺陷。IGRT后感染率和住院率显著降低(p < 0.001);重症监护病房住院率也显著下降(从78.5%降至21.4%)。三名氧依赖患者中有两名在这方面表现出改善。在随访期间,有两名患者的临床改善显著,因此停止了IGRT。结论:小儿罕见综合征和复发性感染患者应考虑免疫学评价。IGRT可能有助于改善这些患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
17
审稿时长
6-12 weeks
期刊介绍: Central European Journal of Immunology is a English-language quarterly aimed mainly at immunologists.
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