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患有恰加斯病患者的 HLA I 类和 II 类分型

HLA class I and II profiles of patients presenting with Chagas' disease.

作者信息

Deghaide N H, Dantas R O, Donadi E A

机构信息

Department of Medicine, School of Medicine of Ribeirão Preto, University of São Paulo, Brazil.

出版信息

Dig Dis Sci. 1998 Feb;43(2):246-52. doi: 10.1023/a:1018829600200.

Abstract

To evaluate the HLA class I and II profiles of a large group of patients with Chagas' disease, 176 patients presenting with pure cardiomyopathy with heart failure (N = 60), cardiomyopathy without heart failure (N = 18), pure digestive tract manifestations (N = 25), cardiac plus digestive disease (N = 40), and asymptomatic patients with positive serology for chronic Trypanosoma cruzi infection (N = 33) were studied. A total of 448 normal individuals were also studied in parallel. HLA class I and II specificities were determined using serology and oligonucleotide analysis. HLA-A30 antigen was overrepresented in the total group and in the subgroups presenting with the pure cardiac (with or without heart failure) or digestive form, conferring similar relative risks and etiologic fractions on all these presentation forms. Serologic HLA class II analysis showed that HLA-DQ1 conferred susceptibility to, while HLA-DQ7 antigen conferred protection against the development of the disease in the total group of patients. Oligonucleotide typing did not confirm the HLA class II associations obtained by serology, but showed that HLA-DQB106 alleles were underrepresented in the total group and in the subgroups presenting with pure digestive or cardiac disease, conferring closely similar relative risks and preventive fractions. Although asymptomatic patients showed a tendency to increased HLA-A30, they presented a significant increase of HLA-DQB10302 specificity. In conclusion, HLA-A30 antigen conferred susceptibility to, while HLA-DQB1*06 specificity conferred protection against, the development of the disease, regardless of the form of presentation, ie, cardiac or digestive tract disease.

摘要

为评估一大群恰加斯病患者的HLA I类和II类谱型,我们研究了176例患者,其中包括伴有心力衰竭的单纯性心肌病患者(N = 60)、无心力衰竭的心肌病患者(N = 18)、单纯消化道表现患者(N = 25)、心脏加消化道疾病患者(N = 40)以及慢性克氏锥虫感染血清学阳性的无症状患者(N = 33)。同时还平行研究了448名正常个体。使用血清学和寡核苷酸分析确定HLA I类和II类特异性。HLA - A30抗原在整个研究组以及呈现单纯心脏型(伴或不伴心力衰竭)或消化道型的亚组中出现频率过高,在所有这些表现形式中赋予相似的相对风险和病因分值。血清学HLA II类分析显示,HLA - DQ1赋予易感性,而HLA - DQ7抗原在整个患者组中赋予对疾病发展的保护作用。寡核苷酸分型未证实血清学获得的HLA II类关联,但显示HLA - DQB106等位基因在整个研究组以及呈现单纯消化道或心脏疾病的亚组中出现频率过低,赋予密切相似的相对风险和预防分值。尽管无症状患者显示出HLA - A30增加的趋势,但他们的HLA - DQB10302特异性显著增加。总之,无论表现形式是心脏疾病还是消化道疾病,HLA - A30抗原赋予疾病易感性,而HLA - DQB1*06特异性赋予疾病发展的保护作用。

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