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日本系统性红斑狼疮患者中补体C4A缺乏症不存在基因缺失情况。

Lack of gene deletion for complement C4A deficiency in Japanese patients with systemic lupus erythematosus.

作者信息

Yamada H, Watanabe A, Mimori A, Nakano K, Takeuchi F, Matsuta K, Tanimoto K, Miyamoto T, Yukiyama Y, Tokunaga K

机构信息

Department of Medicine and Physical Therapy, School of Medicine, University of Tokyo, Fujitsu Kawasaki Hospital, Japan.

出版信息

J Rheumatol. 1990 Aug;17(8):1054-7.

PMID:1976809
Abstract

The frequency of C4A gene deletion was studied in Japanese patients with systemic lupus erythematosus (SLE) and was compared with healthy controls. DNA preparations were extracted from peripheral blood leukocytes from 59 patients with SLE and from 166 healthy persons, and digested by restriction enzymes. They were hybridized with C4 complementary DNA by the Southern blotting method and the deletion of C4A gene was judged from restriction fragment length polymorphism. At the same time phenotypic C4A deficiency (C4AQ0) was measured. Our results showed that the frequency of phenotypic C4A deficiency was 44.1% in Japanese patients with SLE and this value was comparable with that (43.2%) in Caucasian patients. On the other hand the deletion of C4A gene was not found in Japanese patients with SLE (0%), or in healthy controls (0.6%). Our results indicate that C4AQ0 may contribute to the pathogenesis of SLE beyond the ethnical differences but Japanese patients with SLE have a different genetic background from Caucasian patients with the C4A gene deleted.

摘要

对日本系统性红斑狼疮(SLE)患者的C4A基因缺失频率进行了研究,并与健康对照者进行了比较。从59例SLE患者和166名健康人的外周血白细胞中提取DNA样本,用限制性内切酶进行消化。采用Southern印迹法与C4互补DNA杂交,根据限制性片段长度多态性判断C4A基因的缺失情况。同时测定表型C4A缺陷(C4AQ0)。我们的结果显示,日本SLE患者中表型C4A缺陷的频率为44.1%,这一数值与白种人患者(43.2%)相当。另一方面,在日本SLE患者(0%)和健康对照者(0.6%)中均未发现C4A基因缺失。我们的结果表明,C4AQ0可能在种族差异之外对SLE的发病机制起作用,但日本SLE患者与C4A基因缺失的白种人患者具有不同的遗传背景。

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