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献血者和狼疮患者中的C2缺乏症:巴西人群中的患病率、临床特征及HLA相关性

C2 deficiency in blood donors and lupus patients: prevalence, clinical characteristics and HLA-associations in the Brazilian population.

作者信息

Araújo M N, Silva N P, Andrade L E, Sato E I, Gerbase-DeLima M, Leser P G

机构信息

Department of Medicine, Universidade Federal de São Paulo, Brazil.

出版信息

Lupus. 1997;6(5):462-6. doi: 10.1177/096120339700600509.

Abstract

The objective of the present study was to investigate the prevalence, clinical characteristics, and HLA association of C2 deficiency in the Brazilian population. The frequency of C2 deficiency profile (C2Q degree profile) was 2.2% among 1503 blood donors and 6.6% among 166 patients with systemic lupus erythematosus (SLE). A higher incidence of clinical manifestations possibly related to immune complex disease was observed among blood donors with C2Q degree profile and their relatives with C2Q degree profile when compared to the normal C2 relatives. The comparison of clinical and laboratory features between SLE patients with C2Q degree profile and those with normal C2 revealed earlier disease onset, higher frequency of oral ulcerations and lower frequency of anti-native DNA antibodies in the first group. The HLA study conducted on 18 individuals with C2Q degree profile (11 blood donors and 7 SLE patients) confirmed the previously reported association with the antigens HLA-A25, B18 and DR2, supporting the concept that probably most C2 deficiency cases, throughout the world, are due to a single mutation in the C2 gene in linkage disequilibrium with the A25B18DR2 haplotype.

摘要

本研究的目的是调查巴西人群中C2缺乏症的患病率、临床特征及与HLA的关联。在1503名献血者中,C2缺乏型(C2Q程度型)的频率为2.2%,在166名系统性红斑狼疮(SLE)患者中为6.6%。与正常C2亲属相比,C2Q程度型献血者及其具有C2Q程度型的亲属中,观察到可能与免疫复合物疾病相关的临床表现发生率更高。对具有C2Q程度型的SLE患者和具有正常C2的患者的临床和实验室特征进行比较,结果显示第一组患者发病更早、口腔溃疡频率更高且抗天然DNA抗体频率更低。对18名具有C2Q程度型的个体(11名献血者和7名SLE患者)进行的HLA研究证实了先前报道的与抗原HLA - A25、B18和DR2的关联,支持了这样一种观点,即全世界可能大多数C2缺乏症病例是由于C2基因中的单个突变与A25B18DR2单倍型处于连锁不平衡状态所致。

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