血液可溶性 CD89-IgA 复合物可能是预测免疫球蛋白 A 血管炎患儿多器官受累,尤其是肾脏受累的潜在生物标志物。

IF 4.8 2区 医学 Q2 IMMUNOLOGY International immunopharmacology Pub Date : 2024-09-05 DOI:10.1016/j.intimp.2024.113063
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引用次数: 0

摘要

背景:免疫球蛋白 A 血管炎(IgAV免疫球蛋白A血管炎(IgAV)是一种由IgA免疫复合物(IgA-IC)介导的全身性血管炎。可溶性CD89-IgA复合物(sCD89-IgA)作为IgAV肾脏受累相关的一种IgA-IC,血液sCD89-IgA作为生物标志物预测IgAV患儿肾脏或多器官受累的能力尚不明显,本研究主要关注于此:方法:收集了 57 名 IgAV 儿童患者的临床特征和血液样本。采用 ELISA 检测血浆 IgA-ICs 和 sCD89-IgA 水平。血清 IgA 水平采用肾盂肾炎测定法检测。对这些患者的性别、年龄、血清 IgA 水平、血浆 IgA-ICs 水平、血浆 sCD89-IgA 水平与包括肾脏在内的多器官(皮肤除外)受累情况之间的关系进行了统计分析:结果:与单纯皮肤受累的患者相比,多器官(尤其是肾脏)受累的患者血浆 IgA-ICs 和 sCD89-IgA 水平更高,且统计学差异显著。此外,高水平的血浆 sCD89-IgA 是患者除皮肤外出现多器官或肾脏受累的高危因素。ROC 曲线分析表明,AUC 为 0.861(灵敏度:83%,特异度:88%,P 结论:血浆 CD89-IgA 水平的高低是导致患者出现皮肤以外的多器官或肾脏受累的高危因素:结果表明,血浆 sCD89-IgA 可能是预测 IgAV 儿科患者多器官(除皮肤外)受累,尤其是肾脏受累的潜在生物标志物。
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Blood soluble CD89-IgA complex may be a potential biomarker for predicting multi-organ involvement, especially renal involvement in children with immunoglobulin A vasculitis

Background

Immunoglobulin A vasculitis (IgAV) is a kind of systemic vasculitis mediated by IgA immune complexes (IgA-ICs). Soluble CD89-IgA complex (sCD89-IgA) as a type of IgA-IC associated with renal involvement in IgAV, the ability of blood sCD89-IgA as a biomarker to predict renal or multi-organ involvement in children with IgAV is not evident, and this study mainly focused on this.

Methods

The clinical characteristics and blood samples of 57 pediatric patients with IgAV were collected. ELISA was used to detect plasma IgA-ICs and sCD89-IgA levels. Serum IgA levels were detected by Nephelometry method. Statistical analysis was conducted to analyze the relationship between sex, age, serum IgA levels, plasma IgA-ICs levels, plasma sCD89-IgA levels and the involvement of multiple organs (except skin) including kidneys in these patients.

Results

Compared to patients with simple skin involvement, patients with multi-organ involvement, especially kidneys, had higher levels of plasma IgA-ICs and sCD89-IgA, and the statistical difference was significant. In addition, a high level of plasma sCD89-IgA was a high-risk factor for patients to develop multi-organ or renal involvement in addition to the skin. ROC curve analysis showed that the AUC was 0.861 (Sensitivity: 83 %, Specificity: 88 %, p < 0.0001) when plasma sCD89-IgA predicted multi-organ involvement, and AUC 0.926 (Sensitivity: 94 %, Specificity: 88 %, p < 0.0001) for predicting renal involvement.

Conclusions

The results suggested that plasma sCD89-IgA may be a potential biomarker for predicting multi-organ involvement (in addition to skin), especially renal involvement in IgAV pediatric patients.

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来源期刊
CiteScore
8.40
自引率
3.60%
发文量
935
审稿时长
53 days
期刊介绍: International Immunopharmacology is the primary vehicle for the publication of original research papers pertinent to the overlapping areas of immunology, pharmacology, cytokine biology, immunotherapy, immunopathology and immunotoxicology. Review articles that encompass these subjects are also welcome. The subject material appropriate for submission includes: • Clinical studies employing immunotherapy of any type including the use of: bacterial and chemical agents; thymic hormones, interferon, lymphokines, etc., in transplantation and diseases such as cancer, immunodeficiency, chronic infection and allergic, inflammatory or autoimmune disorders. • Studies on the mechanisms of action of these agents for specific parameters of immune competence as well as the overall clinical state. • Pre-clinical animal studies and in vitro studies on mechanisms of action with immunopotentiators, immunomodulators, immunoadjuvants and other pharmacological agents active on cells participating in immune or allergic responses. • Pharmacological compounds, microbial products and toxicological agents that affect the lymphoid system, and their mechanisms of action. • Agents that activate genes or modify transcription and translation within the immune response. • Substances activated, generated, or released through immunologic or related pathways that are pharmacologically active. • Production, function and regulation of cytokines and their receptors. • Classical pharmacological studies on the effects of chemokines and bioactive factors released during immunological reactions.
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