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先天模式识别受体的多态性、对干扰素-β的反应以及多发性硬化症患者中和抗体的产生。

Polymorphisms of innate pattern recognition receptors, response to interferon-beta and development of neutralizing antibodies in multiple sclerosis patients.

机构信息

Institute for Inflammation Research, Department of Rheumatology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

出版信息

Mult Scler. 2010 Aug;16(8):942-9. doi: 10.1177/1352458510373264. Epub 2010 Jul 1.

Abstract

BACKGROUND

Interferon-beta therapy of patients with relapsing-remitting multiple sclerosis involves repeated 'immunizations' with exogenous protein solutions. Innate pattern recognition receptors play an important role in immune responses towards foreign substances and may thus be related to treatment outcome.

OBJECTIVE

To determine the genotypes at 42 single nucleotide polymorphism loci in selected pattern recognition receptors for 567 prospectively followed relapsing-remitting multiple sclerosis patients treated with recombinant interferon-beta, and test for relationships to several outcome parameters, including formation of interferon-beta neutralizing antibodies.

RESULTS

The results suggest an association between the rs5743810 polymorphism (Ser249Pro) of TLR6 and development of neutralizing antibodies after 24 months of therapy in males (p = 0.00002), but not in females (p = 0.2). This association survived crude Bonferroni correction (p (corrected) = 0.02). Additional associations were observed in carriers of the TLR2-rs5743708 and NOD2-rs3135499 SNPs (time to relapse), the TLR7-rs179008 and NOD1-rs2075820 SNPs (time to disease progression) and the TLR4-rs7873784, TLR9-rs5743836, and NOD2-rs2066842 SNPs (frequency of neutralizing antibodies development). All of these, however, failed to survive correction for multiple testing. There were no significant differences between interferon-beta responders and non-responders for any of the investigated single nucleotide polymorphisms.

CONCLUSIONS

The rs5743810 polymorphism of TLR6 may be involved in development of anti-interferon-beta antibodies in males, although further studies are required to firmly establish this.

摘要

背景

对复发缓解型多发性硬化症患者的干扰素-β治疗涉及反复使用外源性蛋白溶液进行“免疫接种”。先天模式识别受体在对外来物质的免疫反应中发挥重要作用,因此可能与治疗结果相关。

目的

确定 567 例接受重组干扰素-β治疗的前瞻性随访复发缓解型多发性硬化症患者中选定的模式识别受体的 42 个单核苷酸多态性位点的基因型,并测试与几个结局参数的关系,包括干扰素-β中和抗体的形成。

结果

研究结果表明,TLR6 的 rs5743810 多态性(Ser249Pro)与男性治疗 24 个月后中和抗体的产生有关(p=0.00002),但与女性无关(p=0.2)。该关联在粗校正的 Bonferroni 校正后仍然存在(p(校正)=0.02)。在 TLR2-rs5743708 和 NOD2-rs3135499 SNP(复发时间)、TLR7-rs179008 和 NOD1-rs2075820 SNP(疾病进展时间)以及 TLR4-rs7873784、TLR9-rs5743836 和 NOD2-rs2066842 SNP(中和抗体产生频率)的携带者中也观察到了其他关联。然而,所有这些都没有通过多重测试校正。在所研究的单核苷酸多态性中,干扰素-β应答者和无应答者之间没有显著差异。

结论

TLR6 的 rs5743810 多态性可能与男性产生抗干扰素-β抗体有关,但需要进一步的研究来确定这一点。

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