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唐氏综合征患者伴或不伴反复感染的不同免疫模式。

Different immunological patterns of Down syndrome patients with and without recurrent infections.

机构信息

Universidade Federal de Uberlândia, Hospital de Clínicas, Uberlândia, MG, Brazil.

Universidade Federal de Uberlândia, Uberlândia, MG, Brazil.

出版信息

J Pediatr (Rio J). 2024 Nov-Dec;100(6):653-659. doi: 10.1016/j.jped.2024.06.007. Epub 2024 Jul 22.

DOI:10.1016/j.jped.2024.06.007
PMID:39053889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11662752/
Abstract

OBJECTIVE

Individuals with Down Syndrome (DS) exhibit a higher susceptibility to infections, suggesting potential immunological alterations within this population. Consequently, this study aims to assess the immune response profile in children with DS to identify potential immune dysfunctions associated with recurrent infections.

METHODS

The authors conducted a retrospective analysis involving 49 DS patients, examining various epidemiological, clinical, cytogenetic, and laboratory variables. The study's sample comprised patients aged 2-20 years, with a predominance of males. These patients were categorized into two groups based on the presence or absence of recurrent infections, as indicated by the Jeffrey Modell Foundation alert signs.

RESULTS

Immunoglobulin (Ig) A, G, and M levels were deemed normal, although individuals with DS experiencing recurrent infections exhibited significantly lower IgA levels. Additionally, CD3, CD4, CD8, and CD19 lymphocyte counts were found to be within normal ranges, with no significant differences between the two groups. While overall data indicated normal seroconversion levels of pneumococcal polysaccharide antibodies, a notable impairment in seroconversion was observed among DS patients with recurrent infections compared to those without such infections.

CONCLUSION

The deficiency of anti-polysaccharide antibodies in individuals with DS may constitute an important immunological comorbidity. Therefore, it warrants further investigation, particularly among individuals with recurrent infections.

摘要

目的

唐氏综合征(DS)患者易感染,提示该人群存在潜在的免疫改变。因此,本研究旨在评估 DS 儿童的免疫反应谱,以确定与反复感染相关的潜在免疫功能障碍。

方法

作者进行了一项回顾性分析,纳入了 49 例 DS 患者,检测了各种流行病学、临床、细胞遗传学和实验室变量。研究样本包括 2-20 岁的患者,男性居多。根据 Jeffrey Modell 基金会的警报标志,这些患者分为有或无反复感染两组。

结果

免疫球蛋白(Ig)A、G 和 M 水平正常,但有反复感染的 DS 患者 IgA 水平显著降低。此外,CD3、CD4、CD8 和 CD19 淋巴细胞计数在正常范围内,两组间无显著差异。虽然肺炎球菌多糖抗体的总血清转化率数据正常,但与无反复感染的 DS 患者相比,有反复感染的 DS 患者的血清转化率显著受损。

结论

DS 患者抗多糖抗体缺乏可能构成重要的免疫合并症。因此,需要进一步研究,特别是在反复感染的患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43dd/11662752/112353707482/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43dd/11662752/112353707482/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43dd/11662752/112353707482/gr1.jpg

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