Department of Rheumatology and Immunology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Clin Rheumatol. 2024 Jan;43(1):189-198. doi: 10.1007/s10067-023-06758-7. Epub 2023 Oct 19.
Systemic lupus erythematosus (SLE) is a complicated autoimmune disease, in which infection is a leading cause of death. Some SLE patients clinically presented with recurrent and refractory infections, which manifested as adult-onset immunodeficiency syndrome due to the production of anti-interferon-γ (anti-IFN-γ) autoantibodies. This study aimed to investigate the role of anti-IFN-γ autoantibodies concerning severe infections in SLE patients.
We detected serum levels of anti-IFN-γ IgG/IgM isotypes in SLE patients with severe infections (n = 55), SLE patients without severe infections (n = 120), rheumatoid arthritis (n = 24), ankylosing spondylitis (n = 24), and healthy controls (n = 60). The relationship between anti-IFN-γ autoantibodies and clinical characteristics and laboratory parameters were analyzed. We further evaluated the neutralizing ability of anti-IFN-γ IgG.
The level of anti-IFN-γ IgG was significantly elevated in SLE patients with severe infections compared with the other groups (all p < 0.01), and the positive rates of anti-IFN-γ IgG in SLE patients with and without severe infections were 29.1% and 10.8%, respectively. Further analysis indicated that the levels of anti-IFN-γ IgG were positively associated with the SLEDAI score (r = 0.6420, p < 0.001), and it could predict the susceptibility to severe infections in SLE patients. Moreover, the inhibition and function assay showed that purified IgG from anti-IFN-γ IgG-positive SLE patients could neutralize IFN-γ, and further impair IFN-γ-induced STAT1 phosphorylation.
The neutralizing anti-IFN-γ IgG might increase the susceptibility to infection in SLE patients, which has important implications for the treatment. Key Points • The role of anti-IFN-γ autoantibodies concerning severe infections in SLE patients remains unknown. • The results of this study reveals that anti-IFN-γ IgG levels were significantly elevated in SLE patients with severe infections. • This study suggests that neutralizing anti-IFN-γ IgG might increase the susceptibility to infection in SLE patients.
系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,感染是导致死亡的主要原因之一。一些 SLE 患者临床表现为反复和难治性感染,由于产生抗干扰素-γ(anti-IFN-γ)自身抗体,表现为成人发病的免疫缺陷综合征。本研究旨在探讨抗 IFN-γ 自身抗体在 SLE 患者严重感染中的作用。
我们检测了 55 例严重感染的 SLE 患者(SLE 合并感染组)、120 例无严重感染的 SLE 患者(SLE 无感染组)、24 例类风湿关节炎患者(RA 组)、24 例强直性脊柱炎患者(AS 组)和 60 例健康对照者(对照组)的血清抗 IFN-γ IgG/IgM 同种型水平。分析了抗 IFN-γ 自身抗体与临床特征和实验室参数的关系。我们进一步评估了抗 IFN-γ IgG 的中和能力。
与其他组相比,SLE 合并感染组患者的抗 IFN-γ IgG 水平显著升高(均 P<0.01),SLE 合并感染组和 SLE 无感染组抗 IFN-γ IgG 的阳性率分别为 29.1%和 10.8%。进一步分析表明,抗 IFN-γ IgG 水平与 SLEDAI 评分呈正相关(r=0.6420,P<0.001),可预测 SLE 患者发生严重感染的易感性。此外,抑制和功能测定表明,来自抗 IFN-γ IgG 阳性的 SLE 患者的纯化 IgG 可中和 IFN-γ,并进一步损害 IFN-γ 诱导的 STAT1 磷酸化。
中和抗 IFN-γ IgG 可能会增加 SLE 患者感染的易感性,这对治疗具有重要意义。
抗 IFN-γ 自身抗体在 SLE 患者严重感染中的作用尚不清楚。
本研究结果表明,SLE 合并感染组患者的抗 IFN-γ IgG 水平显著升高。
本研究提示中和抗 IFN-γ IgG 可能会增加 SLE 患者感染的易感性。