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在接触过寄生虫感染的人群中,可溶性 CD23 水平与特应性和寄生虫特异性 IgE 水平呈负相关,但与多克隆 IgE 水平无关。

Soluble CD23 levels are inversely associated with atopy and parasite-specific IgE levels but not with polyclonal IgE levels in people exposed to helminth infection.

机构信息

Institute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Ashworth Laboratories, Edinburgh, UK.

出版信息

Int Arch Allergy Immunol. 2013;161(4):333-41. doi: 10.1159/000346545. Epub 2013 May 14.

DOI:10.1159/000346545
PMID:23689700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3795451/
Abstract

BACKGROUND

Protective acquired immunity against helminths and allergic sensitisation are both characterised by high IgE antibody levels. Levels of IgE antibodies are naturally tightly regulated by several mechanisms including binding of the CD23 receptor. Following observations that helminth infections and allergic sensitisation may co-present, the current study aims to investigate the relationship between the soluble CD23 (sCD23) receptor, parasite-specific IgE responses and allergic sensitisation in people exposed to the helminth parasite Schistosoma haematobium.

METHODS

A cohort of 434 participants was recruited in two villages with different levels of S. haematobium infection in Zimbabwe. Serum levels of the 25-kDa fragment of sCD23 were related to levels of schistosome infection intensity, allergen (house dust mite, HDM) and schistosome-specific IgE, total IgE and skin sensitisation to HDM.

RESULTS

sCD23 levels rose significantly with schistosome infection intensity but declined significantly with schistosome-specific IgE levels. Furthermore, sCD23 levels were negatively associated with skin sensitisation and IgE reactivity against HDM, but showed no relationship with total IgE.

CONCLUSION

The results are consistent with the suppression of parasite and allergen-specific IgE levels by sCD23. Further mechanistic studies will determine the relevance of this potential regulatory mechanism in the development of helminth-specific immune responses in atopic individuals.

摘要

背景

针对寄生虫的保护性获得性免疫和过敏敏化都以高 IgE 抗体水平为特征。IgE 抗体的水平自然受到包括 CD23 受体结合在内的多种机制的严格调控。鉴于寄生虫感染和过敏敏化可能同时存在的观察结果,本研究旨在调查在接触寄生虫 Schistosoma haematobium 的人群中,可溶性 CD23(sCD23)受体、寄生虫特异性 IgE 反应与过敏敏化之间的关系。

方法

在津巴布韦两个具有不同 S. haematobium 感染水平的村庄招募了 434 名参与者。sCD23 的 25-kDa 片段的血清水平与寄生虫感染强度、过敏原(屋尘螨,HDM)和寄生虫特异性 IgE、总 IgE 以及对 HDM 的皮肤致敏相关。

结果

sCD23 水平随着寄生虫感染强度的增加而显著升高,但随着寄生虫特异性 IgE 水平的升高而显著降低。此外,sCD23 水平与皮肤致敏和对 HDM 的 IgE 反应呈负相关,但与总 IgE 无关。

结论

这些结果与 sCD23 抑制寄生虫和过敏原特异性 IgE 水平的结果一致。进一步的机制研究将确定这种潜在的调节机制在特应性个体中针对寄生虫特异性免疫反应的发展中的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/b156d0b5daf3/iaa-0161-0333-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/0d0870dcce5b/iaa-0161-0333-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/ceb8720cde28/iaa-0161-0333-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/859a407cbed4/iaa-0161-0333-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/374a2c92d4ae/iaa-0161-0333-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/b156d0b5daf3/iaa-0161-0333-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/0d0870dcce5b/iaa-0161-0333-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/ceb8720cde28/iaa-0161-0333-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/859a407cbed4/iaa-0161-0333-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/374a2c92d4ae/iaa-0161-0333-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9c/3795451/b156d0b5daf3/iaa-0161-0333-g05.jpg

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2
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