澳大利亚慢性疲劳综合征/肌痛性脑脊髓炎患者自然杀伤细胞免疫球蛋白样受体基因型和单倍型研究

Gene regulation and systems biology Pub Date : 2016-06-19 eCollection Date: 2016-01-01 DOI:10.4137/GRSB.S39861
T K Huth, E W Brenu, D R Staines, S M Marshall-Gradisnik
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引用次数: 1

摘要

杀伤细胞免疫球蛋白样受体(KIR)基因编码表面受体的激活和抑制,与自然杀伤细胞(NK)细胞毒性活性的调节有关。慢性疲劳综合征/肌痛性脑脊髓炎(CFS/ME)患者一直有NK细胞毒性活性降低的报道,KIR单倍型和等位基因多态性仍有待研究。本文的目的是开展一项初步研究,以检查CFS/ME患者和非疲劳对照(nfc)的KIR基因型、单倍型和等位基因多态性。比较20例CFS/ME患者与20例nfc患者的KIR和等位基因多态性频率无显著差异。与nfc相比,CFS/ME患者端粒A/B基序的频率较低(P < 0.05)。这项初步研究首次报道了CFS/ME患者端粒A/B基序上KIR频率的差异。需要在更大的CFS/ME队列中进行进一步的研究来验证这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Killer Cell Immunoglobulin-like Receptor Genotype and Haplotype Investigation of Natural Killer Cells from an Australian Population of Chronic Fatigue Syndrome/Myalgic Encephalomyelitis Patients.

Killer Cell Immunoglobulin-like Receptor Genotype and Haplotype Investigation of Natural Killer Cells from an Australian Population of Chronic Fatigue Syndrome/Myalgic Encephalomyelitis Patients.

Killer Cell Immunoglobulin-like Receptor Genotype and Haplotype Investigation of Natural Killer Cells from an Australian Population of Chronic Fatigue Syndrome/Myalgic Encephalomyelitis Patients.

Killer cell immunoglobulin-like receptor (KIR) genes encode for activating and inhibitory surface receptors, which are correlated with the regulation of Natural Killer (NK) cell cytotoxic activity. Reduced NK cell cytotoxic activity has been consistently reported in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) patients, and KIR haplotypes and allelic polymorphism remain to be investigated. The aim of this article was to conduct a pilot study to examine KIR genotypes, haplotypes, and allelic polymorphism in CFS/ME patients and nonfatigued controls (NFCs). Comparison of KIR and allelic polymorphism frequencies revealed no significant differences between 20 CFS/ME patients and 20 NFCs. A lower frequency of the telomeric A/B motif (P < 0.05) was observed in CFS/ME patients compared with NFCs. This pilot study is the first to report the differences in the frequency of KIR on the telomeric A/B motif in CFS/ME patients. Further studies with a larger CFS/ME cohort are required to validate these results.

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