Levels of Natural Antibodies Before and After Immunoglobulin Replacement Treatment Affect the Clinical Phenotype in Common Variable Immunodeficiency.

IF 7.2 2区 医学 Q1 IMMUNOLOGY
Ioannis Sarrigeorgiou, Gerasimina Tsinti, Fani Kalala, Anastasios Germenis, Matthaios Speletas, Peggy Lymberi
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引用次数: 0

Abstract

Natural antibodies (NAbs) occurring in individuals without prior exposure to specific antigens, provide direct first barrier protection against pathogens, and exert immunoregulation thus actively contributing to the maintenance of immune homeostasis, controlling inflammatory processes and preventing autoimmunity. Common variable immunodeficiency (CVID) is a heterogeneous group of disorders characterized by a compromised immune function that brings into focus the role of NAbs. Our aim was to explore whether NAb levels could serve as potential key indicators in CVID for monitoring disease progression and predicting outcomes. In this study, we analyzed a Hellenic cohort of 56 patients with CVID (31 newly diagnosed and 25 under immunoglobulin replacement therapy-IgRT) and 33 healthy controls, for total Ig levels and serum IgM and IgG NAb levels against five informative target-antigens of NAbs, namely, actin, DNA, carbonic anhydrase, F(ab΄)2 fragments of human IgG and TriNitroPhenyl. In addition, follow-up pre- and post- IgRT samples were analyzed in ten (10) patients of our cohort. Results showed that Ig-treated patients exhibited significantly lower IgM NAb levels than untreated patients and healthy controls against all panel antigens. In the follow-up samples, pre-treatment IgM NAb levels negatively correlated with total serum IgM. This imbalance was only partially restored after IgRT, with a significant decrease in IgM NAb levels observed in nine out of ten patients. Moreover, post-treatment patients with recurrent infections presented significantly lower IgM NAb levels, a reduction also observed in patients with bronchiectasis independently of treatment status. On the contrary, post-treatment patients with enteropathy had significantly higher IgM NAb levels against all panel antigens, an increase also noted in patients with autoimmune diseases. Regarding IgG NAbs, replacement therapy restored levels to those of healthy controls. In conclusion, impaired NAb levels are found in CVID patients, particularly related to certain phenotypes. Moreover, the significant decrease in IgM NAb levels after IgRT suggests a potential association with disease course and complications. The results suggest that administration of human IgM NAbs may be an effective combinatorial treatment in selected patients. Further research is needed to understand the functional roles of NAbs in CVID and its complex clinical phenotypes.

免疫球蛋白替代治疗前后的天然抗体水平会影响常见变异性免疫缺陷病的临床表型。
天然抗体(NAbs)产生于未接触过特定抗原的个体,可直接提供抵御病原体的第一道屏障,并发挥免疫调节作用,从而积极促进免疫平衡的维持、控制炎症过程和预防自身免疫。常见变异性免疫缺陷症(CVID)是一组以免疫功能受损为特征的异质性疾病,它使人们开始关注NAb的作用。我们的目的是探索 NAb 水平是否可作为 CVID 的潜在关键指标,用于监测疾病进展和预测预后。在这项研究中,我们分析了希腊队列中的 56 名 CVID 患者(31 名新确诊患者和 25 名接受免疫球蛋白替代疗法-IgRT 的患者)和 33 名健康对照者的总 Ig 水平以及血清 IgM 和 IgG NAb 水平,这些 NAb 针对五种信息丰富的目标抗原,即肌动蛋白、DNA、碳酸酐酶、人类 IgG 的 F(ab΄)2 片段和三硝基苯。此外,我们还对队列中十(10)名患者的 IgRT 治疗前后的随访样本进行了分析。结果显示,接受过 Ig 治疗的患者针对所有抗原的 IgM NAb 水平明显低于未接受治疗的患者和健康对照组。在随访样本中,治疗前的 IgM NAb 水平与血清总 IgM 呈负相关。这种不平衡在 IgRT 治疗后仅得到部分恢复,10 例患者中有 9 例的 IgM NAb 水平显著下降。此外,治疗后反复感染的患者的 IgM NAb 水平明显降低,支气管扩张症患者的 IgM NAb 水平也出现下降,与治疗情况无关。相反,治疗后的肠病患者针对所有抗原的 IgM NAb 水平明显升高,自身免疫性疾病患者的 IgM NAb 水平也有所升高。至于 IgG NAb,替代疗法可使其水平恢复到健康对照组的水平。总之,CVID 患者的 NAb 水平受损,尤其与某些表型有关。此外,IgRT 后 IgM NAb 水平的显著下降表明,这可能与病程和并发症有关。研究结果表明,对特定患者施用人类 IgM NAb 可能是一种有效的综合治疗方法。要了解 NAbs 在 CVID 及其复杂临床表型中的功能作用,还需要进一步的研究。
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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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