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首页> 外文期刊>European journal of immunogenetics: official journal of the British Society for Histocompatibility and Immunogenetics >Immunoregulatory cytokine polymorphisms in Italian patients affected by paroxysmal nocturnal haemoglobinuria and aplastic anaemia.
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Immunoregulatory cytokine polymorphisms in Italian patients affected by paroxysmal nocturnal haemoglobinuria and aplastic anaemia.

机译:受阵发性夜间血红蛋白尿和再生障碍性贫血影响的意大利患者的免疫调节细胞因子多态性。

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摘要

Summary We investigated regulatory variants of five cytokine genes [tumour necrosis factor (TNF)-alpha, interferon (IFN)-gamma, transforming growth factor (TGF)-beta, interleukin (IL)-6 and IL-10] in 40 Italian patients affected by paroxysmal nocturnal haemoglobinuria (PNH) and aplastic anaemia (AA). Genotypes associated with high production of TGF-beta and IFN-gamma were more frequent in patients than in controls. Genetic regulation of the immunological pathways involved in the pathogenesis of bone marrow failure is suggested.
机译:总结我们调查了40位意大利患者的5种细胞因子基因[肿瘤坏死因子(TNF)-α,干扰素(IFN)-γ,转化生长因子(TGF)-β,白介素(IL)-6和IL-10]的调控变异体。受阵发性夜间血红蛋白尿(PNH)和再生障碍性贫血(AA)的影响。与对照组相比,患者中与TGF-β和IFN-γ高产生相关的基因型更为常见。建议对涉及骨髓衰竭的发病机理的免疫途径进行遗传调控。

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