Hu Congqi, Liu Lingjie, Xiao Hui, Zhao Hongjun, Chen Guangxing, Xie Yanli
Department of Rheumatology Nephrology, Baiyun Hospital The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
First Clinical Medical School, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Front Immunol. 2025 Jun 26;16:1593770. doi: 10.3389/fimmu.2025.1593770. eCollection 2025.
Takayasu arteritis (TAK) is an idiopathic systemic disease characterized by granulomatous inflammation of the aorta and its branches. TAK can cause multiple vascular injuries throughout the body, mainly arterial stenosis and aneurysms. In severe cases, it can even lead to fatal hemorrhage, infarction and other serious complications, posing a serious threat to the patient's life and health. Few studies have shown that drug treatment can improve or reverse its vascular stenosis. This study describes a 19-year-old woman diagnosed with TAK who had multiple vascular stenosis at the time of the disease. In an early and timely manner as well as up to seven years after a full course of tolizumab, her vascular wall thickening improved and previously stenotic vessels were recanalized. We believe that early use of tocilizumab in patients with TAK can improve vascular lesions. To our knowledge, this study is the first case to find complete recanalization of stenotic vessels after the use of tocilizumab, and the pre- and post-test and examination data are complete. In addition, we summarized the cases of improvement of vascular lesions after tocilizumab treatment of TAK, and preliminarily compared the efficacy and safety of tocilizumab and TNFi in TAK. We speculate that early and adequate use of tocilizumab could reverse early inflammatory vessel wall thickening and stenosis, and we found, through further literature review, that its efficacy was comparable to that of TNF inhibitors.
大动脉炎(TAK)是一种特发性全身性疾病,其特征为主动脉及其分支的肉芽肿性炎症。TAK可导致全身多处血管损伤,主要是动脉狭窄和动脉瘤。在严重情况下,甚至可导致致命性出血、梗死及其他严重并发症,对患者的生命健康构成严重威胁。很少有研究表明药物治疗能够改善或逆转其血管狭窄。本研究描述了一名19岁诊断为TAK的女性,在疾病发生时存在多处血管狭窄。在早期及时以及使用托珠单抗全疗程后长达七年的时间里,她的血管壁增厚情况得到改善,先前狭窄的血管实现了再通。我们认为,在TAK患者中早期使用托珠单抗可改善血管病变。据我们所知,本研究是首例发现使用托珠单抗后狭窄血管实现完全再通的病例,且前后检测及检查数据完整。此外,我们总结了托珠单抗治疗TAK后血管病变改善的病例,并初步比较了托珠单抗和肿瘤坏死因子抑制剂(TNFi)在TAK中的疗效和安全性。我们推测,早期且充分使用托珠单抗可逆转早期炎症性血管壁增厚和狭窄,并且通过进一步文献回顾发现,其疗效与肿瘤坏死因子抑制剂相当。