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法裔加拿大儿童侵袭性 A 组链球菌病与 MyD88/IRAK4 通路缺陷无关。

Invasive group A Streptococcus disease in French-Canadian children is not associated with a defect in MyD88/IRAK4-pathway.

机构信息

Department of Microbiology, Infectiology and Immunology, CHU Sainte-Justine and University of Montreal, Montreal (Quebec), Canada.

出版信息

Allergy Asthma Clin Immunol. 2014 Feb 5;10(1):9. doi: 10.1186/1710-1492-10-9.

DOI:10.1186/1710-1492-10-9
PMID:24499202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3927219/
Abstract

BACKGROUND

Beta-hemolytic Group A Streptococcus invasive disease (iGASd) has been subject to intense research since its re-emergence in the late 1980s. In Quebec, an increase in the number of severe iGASd cases has recently been observed. Because of the inter-individual variability in the severity of iGASd, a hereditary predisposition to invasive disease can be suspected. Given that iGASd occurs in MyD88- and IRAK4-deficient patients, although rarely, the increasing frequency of iGASd in the population of French-Canadian children may be associated with a deficiency in the host's innate immune response.

METHODS

In this report, we assessed the influence of: (i) bacterial genotype and virulence factors, (ii) immune-cellular features, and (iii) Myd88/IRAK4-dependent response to GAS in vitro on the susceptibility to iGASd in a paediatric cohort of 16 children: 11 French-Canadian and 5 from diverse origin.

FINDINGS

GAS virulence factors and genotype are not implicated in the susceptibility toward iGASd, and cellular and MyD88/IRAK4 deficiencies are excluded in our patients.

CONCLUSIONS

Although it has been shown that the MyD88/IRAK4-dependent signal is involved in the response to invasive GAS, our data indicates that a MyD88/IRAK4-mediated signalling defect is not the main factor responsible for the susceptibility to severe iGASd in a paediatric population from the province of Quebec.

摘要

背景

自 20 世纪 80 年代末重新出现以来,β 溶血性 A 组链球菌侵袭性疾病(iGASd)一直是研究的热点。在魁北克,最近观察到严重 iGASd 病例数量增加。由于 iGASd 的个体间严重程度存在差异,因此可以怀疑存在侵袭性疾病的遗传易感性。鉴于 iGASd 发生在 MyD88 和 IRAK4 缺陷患者中,尽管很少见,但法裔加拿大儿童人群中 iGASd 的发病率增加可能与宿主固有免疫反应的缺陷有关。

方法

在本报告中,我们评估了以下因素对 16 名儿童(11 名法裔加拿大儿童和 5 名来自不同种族的儿童)的 iGASd 易感性的影响:(i)细菌基因型和毒力因子,(ii)免疫细胞特征,和(iii)体外 GAS 对 Myd88/IRAK4 的反应:

结果

GAS 毒力因子和基因型与 iGASd 的易感性无关,并且在我们的患者中排除了细胞和 MyD88/IRAK4 缺乏。

结论

尽管已经表明 MyD88/IRAK4 依赖性信号参与了对侵袭性 GAS 的反应,但我们的数据表明,MyD88/IRAK4 介导的信号缺陷不是导致魁北克省儿科人群发生严重 iGASd 的主要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f8d/3927219/eb8b7a2a5b78/1710-1492-10-9-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f8d/3927219/eb8b7a2a5b78/1710-1492-10-9-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f8d/3927219/eb8b7a2a5b78/1710-1492-10-9-1.jpg

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