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盘尾丝虫病中的免疫球蛋白κ链同种异型(KM)

Immunoglobulin kappa chain allotypes (KM) in onchocerciasis.

作者信息

Pandey J P, Elson L H, Sutherland S E, Guderian R H, Araujo E, Nutman T B

机构信息

Department of Microbiology, Medical University of South Carolina, Charleston 29425, USA.

出版信息

J Clin Invest. 1995 Dec;96(6):2732-4. doi: 10.1172/JCI118341.

Abstract

GM and KM allotypes, powerful tools for genetic characterization of human populations, have been shown to play an important role in genetic predisposition to some infectious diseases. Two diverse racial groups--Afro-Ecuadorians and Amerindians--living in a single restricted geographical area of Ecuador, appear to have different risk factors for acquisition and clinical expression of onchocerciasis, a disease caused by the filarial parasite Onchocerca volvulus. In this study, GM and KM allotypes were determined in 25 Afro-Ecuadorians and 24 Amerindians infected with Onchocerca volvulus (INF) and in putative immune individuals (PI). In Afro-Ecuadorians, the frequency of the homozygous KM 3 phenotype was significantly decreased in INF as compared with the PI group (20 vs. 68%; P= 0.0012), while the frequency of the heterozygous KM 1,3 phenotype was increased in INF as compared with the PI subjects (48 vs. 9%; P= 0.0044). These results suggest that in Afro-Ecuadorians KM 3 is associated with a lower relative risk (resistance), whereas KM 1,3 is associated with an increased risk (susceptibility) of onchocerciasis.

摘要

GM和KM同种异型是用于人类群体基因特征分析的有力工具,已被证明在某些传染病的遗传易感性中发挥重要作用。生活在厄瓜多尔一个有限地理区域内的两个不同种族群体——非裔厄瓜多尔人和美洲印第安人——似乎在盘尾丝虫病(一种由丝虫寄生虫盘尾丝虫引起的疾病)的感染和临床表现方面存在不同的风险因素。在本研究中,对25名感染盘尾丝虫的非裔厄瓜多尔人、24名感染盘尾丝虫的美洲印第安人(感染组)以及假定的免疫个体(PI)进行了GM和KM同种异型的测定。在非裔厄瓜多尔人中,与PI组相比,感染组中纯合KM 3表型的频率显著降低(20%对68%;P = 0.0012),而与PI个体相比,感染组中杂合KM 1,3表型的频率增加(48%对9%;P = 0.0044)。这些结果表明,在非裔厄瓜多尔人中,KM 3与较低的相对风险(抗性)相关,而KM 1,3与盘尾丝虫病的风险增加(易感性)相关。

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本文引用的文献

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Immune responsiveness and the pathogenesis of human onchocerciasis.
J Infect Dis. 1995 Mar;171(3):659-71. doi: 10.1093/infdis/171.3.659.
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Association between maternal Gm allotype and neonatal septicaemia with group B streptococci.
J Immunogenet. 1982 Apr;9(2):143-7. doi: 10.1111/j.1744-313x.1982.tb00975.x.

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