首页> 外文期刊>Immunological Investigations: A Journal of Molecular and Cellular Immunology >Polymorphism of costimulatory molecules (CTLA4, ICOS, PD.1 and CD28) and allogeneic hematopoietic stem cell transplantation in Iranian patients
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Polymorphism of costimulatory molecules (CTLA4, ICOS, PD.1 and CD28) and allogeneic hematopoietic stem cell transplantation in Iranian patients

机译:伊朗患者共刺激分子(CTLA4,ICOS,PD.1和CD28)的多态性和同种异体造血干细胞移植

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摘要

Costimulatory molecules are important factors determining the outcome of bone marrow transplant. Because the host ability in costimulatory molecule function may be affected by gene polymorphisms, the aim of the present study was to investigate the effect of CTLA4, ICOS, PD.1 and CD28 gene polymorphisms in outcome of bone marrow transplant patients. A total of 72 recipients were included in this study. CTLA4 (-1722, -1661, -318, + 49), ICOS (+ 1720), CD28 (+ 17) and PD.1 (PD. 1.3, PD. 1.9) gene polymorphisms were evaluated by PCR-RFLP. The results showed that no differences in the distribution of all mentioned costimulatory molecules genotypes and alleles were observed in the Graft Versus Host Disease (GVHD) group compared to the non-GVHD group. After gender classification, there is a significant association between GA genotype (CTLA4-1661) in male group with GVHD than without GVHD (p = 0.03). Also, in this study we found significant associations between CC genotype and C allele of PD. 1.9, and TT genotype and T allele of CD28 that had more frequency in grades 2-4 (p = 0.04. p = 0.02, p = 0.01, p = 0.003, respectively). Results indicate that the CC genotype and C allele of PD. 1.9 and TT genotype and the T allele of CD28 are genetic risk factors for development of a severe grade of GVHD. This subject needs to be studied in different population.
机译:共刺激分子是决定骨髓移植结果的重要因素。由于共刺激分子功能的宿主能力可能受基因多态性的影响,因此本研究的目的是研究CTLA4,ICOS,PD.1和CD28基因多态性对骨髓移植患者预后的影响。这项研究总共包括72位接受者。通过PCR-RFLP评估了CTLA4(-1722,-1661,-318,+ 49),ICOS(+ 1720),CD28(+ 17)和PD.1(PD.1.3,PD.1.9)基因多态性。结果表明,与非GVHD组相比,移植物抗宿主病(GVHD)组中未观察到所有上述共刺激分子基因型和等位基因的分布差异。性别分类后,患有GVHD的男性组中GA基因型(CTLA4-1661)与没有GVHD的男性组之间存在显着关联(p = 0.03)。此外,在这项研究中,我们发现CC基因型与PD的C等位基因之间存在显着关联。 1.9,以及CD28的TT基因型和T等位基因在2-4级中具有更高的频率(分别为p = 0.04,p = 0.02,p = 0.01,p = 0.003)。结果表明PD的CC基因型和C等位基因。 1.9和TT基因型以及CD28的T等位基因是严重GVHD发生的遗传危险因素。该主题需要在不同的人群中进行研究。

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