Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing, China.
Front Immunol. 2023 Feb 24;14:1091336. doi: 10.3389/fimmu.2023.1091336. eCollection 2023.
Systemic autoinflammatory diseases (SAIDs) are a group of rare diseases characterized by recurrent or continuous inflammation, typically accompanied by genetic variants. Good responses to anti-TNF therapy were observed in SAIDs patients. However, the mechanisms underlying the disease flare and the response to TNF blocking therapy have not been fully elucidated. Here, single-cell RNA sequencing technology was used to describe the transcriptomic profile of PBMCs and PMNs in two SAID patients both before and after anti-TNF treatment. Interferon responses were involved in the disease flare. After anti-TNF therapy, clinical symptoms were alleviated while TNF and IL-1 were unexpectedly increased, indicating that these inflammatory cytokines are not positively correlated with disease activity. Trajectory analysis showed that inhibition of macrophage differentiation, rather than reduction of the inflammatory cytokines, as the potential mechanism of anti-TNF treatment response in SAIDs.
系统性自身炎症性疾病(SAIDs)是一组罕见疾病,其特征为反复或持续的炎症,通常伴有遗传变异。SAIDs 患者对抗 TNF 治疗有良好的反应。然而,疾病发作和 TNF 阻断治疗反应的机制尚未完全阐明。在这里,使用单细胞 RNA 测序技术描述了两名 SAID 患者在抗 TNF 治疗前后 PBMC 和 PMN 的转录组特征。干扰素反应参与了疾病发作。抗 TNF 治疗后,临床症状缓解,而 TNF 和 IL-1 却意外增加,表明这些炎症细胞因子与疾病活动度无正相关性。轨迹分析表明,抑制巨噬细胞分化,而不是减少炎症细胞因子,可能是 SAIDs 抗 TNF 治疗反应的潜在机制。