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子痫前期患者免疫调节基因多态性。

Immunoregulatory gene polymorphisms in women with preeclampsia.

机构信息

Department of Obstetrics, São Paulo Federal University, São Paulo, Brazil.

出版信息

Hypertens Res. 2011 Mar;34(3):384-8. doi: 10.1038/hr.2010.247. Epub 2010 Dec 16.

Abstract

The costimulatory molecules CD28, cytotoxic T-lymphocyte antigen-4 (CTLA-4) (cytotoxic T-lymphocyte-associated antigen-4) and inducible costimulator (ICOS) are believed to have a critical modulatory role in the immune response. However, few studies have been performed on the role of these immune regulatory molecules and their polymorphisms in women with preeclampsia (PE). The aim of our study was to evaluate the CTLA4 (+49 A/G) (rs 231775), CD28 (+17 T/C) (rs 3116496) and ICOS (-1564 T/C) (rs 4675378) gene polymorphisms in Brazilian women with PE. This case-control study included 130 patients with PE and 261 control women without any obstetric or systemic disorders. Genomic DNA was extracted from peripheral blood, and the polymorphism genotyping was performed by digesting the PCR products with the restriction endonucleases BbvI (CTLA-4), AfeI (CD28) and AluI (ICOS). Data were analyzed by χ(2) or Fisher's exact test; a P-value of <0.05 was considered as significant. There were significant differences in the ICOS genotype and allelic frequencies between the PE and control groups (P=0.01 and P=0.01, respectively). We found a significantly lower frequency of the ICOS (-1564) T allele in women with mild PE compared with the controls. There were no differences in the CTLA-4 (+49 A/G) and CD28 (+17 T/C) genotypes and allelic frequencies between the PE patients and controls. Our data suggest that PE is associated with ICOS, but is not associated with the CTLA-4 or CD28 gene polymorphisms.

摘要

共刺激分子 CD28、细胞毒性 T 淋巴细胞抗原-4(CTLA-4)(细胞毒性 T 淋巴细胞相关抗原-4)和诱导共刺激分子(ICOS)被认为在免疫反应中具有关键的调节作用。然而,关于这些免疫调节分子及其多态性在子痫前期(PE)女性中的作用的研究较少。我们的研究目的是评估巴西 PE 女性 CTLA4(+49A/G)(rs231775)、CD28(+17T/C)(rs3116496)和 ICOS(-1564T/C)(rs4675378)基因多态性。这项病例对照研究包括 130 例 PE 患者和 261 例无产科或系统性疾病的对照女性。从外周血中提取基因组 DNA,通过用限制性内切酶 BbvI(CTLA-4)、AfeI(CD28)和 AluI(ICOS)消化 PCR 产物进行基因多态性基因分型。通过 χ(2)或 Fisher 确切检验进行数据分析;P 值<0.05 被认为具有统计学意义。PE 组和对照组之间 ICOS 基因型和等位基因频率存在显著差异(P=0.01 和 P=0.01)。我们发现轻度 PE 女性 ICOS(-1564)T 等位基因的频率明显低于对照组。PE 患者和对照组之间 CTLA-4(+49A/G)和 CD28(+17T/C)基因型和等位基因频率无差异。我们的数据表明,PE 与 ICOS 相关,但与 CTLA-4 或 CD28 基因多态性无关。

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