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常见变异性免疫缺陷与罕见复杂结缔组织和肌肉骨骼疾病的关联。系统文献回顾。

Association of common variable immunodeficiency and rare and complex connective tissue and musculoskeletal diseases. A systematic literature review.

机构信息

Policlinic and Hiller Research Unit for Rheumatology, ERN-ReCONNET member, University Clinic Duesseldorf, Heinrich-Heine-University Duesseldorf, Germany.

ERN-ReCONNET Patient Advocacy Group Advocate, and Lupus Europe, Brussels, Belgium.

出版信息

Clin Exp Rheumatol. 2022 May;40 Suppl 134(5):40-45. doi: 10.55563/clinexprheumatol/bbuvih. Epub 2022 Mar 28.

Abstract

OBJECTIVES

To perform a systematic literature review (SLR) on the association of common variable immunodeficiency (CVID) and rare and complex connective tissue and musculoskeletal diseases, namely systemic lupus erythematosus (SLE), Sjögren's syndrome (SS), idiopathic inflammatory myopathies (IIM), systemic sclerosis (SSc), relapsing polychondritis, antiphospholipid syndrome, immunoglobulin (Ig) G4-related disease, as well as undifferentiated and mixed connective tissue disease.

METHODS

An SLR on studies and cases about the association of CVID and rare and complex connective tissue and musculoskeletal diseases was performed. Animal studies were excluded.

RESULTS

170 publications fulfilled the inclusion criteria. Sjögren's syndrome was the most frequent connective tissue disease in CVID-patients. Most case reports exist on SLE and CVID with SLE mostly preceding the manifestation of CVID. Multiple cases were published reporting the concurrence of CVID and inclusion body myositis and single cases were found on CVID and antisynthetase syndrome, polymyositis, limited SSc and relapsing polychondritis, respectively. There are no cases of CVID and antiphospholipid syndrome, IgG4-related disease, as well as undifferentiated and mixed connective tissue disease.

CONCLUSIONS

The concurrence of CVID and complex connective tissue and musculoskeletal diseases, especially SS, IIM, SSc and relapsing polychondritis is rare but relevant. The measurements of Ig-levels should be performed before the initiation of immunosuppressive therapy to allow for the differentiation of primary and secondary Ig-deficiency and substitute IG if necessary.

摘要

目的

对普通可变免疫缺陷(CVID)与罕见和复杂结缔组织及肌肉骨骼疾病(即系统性红斑狼疮(SLE)、干燥综合征(SS)、特发性炎性肌病(IIM)、系统性硬化症(SSc)、复发性多软骨炎、抗磷脂综合征、免疫球蛋白(Ig)G4 相关疾病以及未分化和混合性结缔组织病)相关的文献进行系统综述(SLR)。

方法

对 CVID 与罕见和复杂结缔组织及肌肉骨骼疾病相关的研究和病例进行 SLR。排除动物研究。

结果

有 170 篇文献符合纳入标准。干燥综合征是 CVID 患者最常见的结缔组织疾病。SLE 是与 CVID 相关的病例报告中最常见的疾病,大多数情况下 SLE 先于 CVID 出现。有多例 CVID 和包涵体肌炎同时发生的报道,也有少数 CVID 和抗合成酶综合征、多发性肌炎、局限型 SSc 和复发性多软骨炎的病例报告。尚未发现 CVID 与抗磷脂综合征、IgG4 相关疾病以及未分化和混合性结缔组织病相关的病例。

结论

CVID 与复杂的结缔组织和肌肉骨骼疾病(尤其是 SS、IIM、SSc 和复发性多软骨炎)同时发生的情况虽然罕见,但很重要。在开始免疫抑制治疗前,应检测 Ig 水平,以便区分原发性和继发性免疫缺陷,并在必要时进行 IG 替代治疗。

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