Meng Jianfen, Jia Jinchao, Gan Ke, Gao Qichen, Chen Longfang, Zhu Dehao, Wang Mengyan, Xiao Yu, Ma Yuning, Chen Xia, Yi Da, Shi Hui, Sun Yue, Liu Honglei, Cheng Xiaobing, Su Yutong, Ye Junna, Chi Huihui, Zhou Zhuochao, Liu Tingting, Du Wei, Zhao Yue, Yang Chengde, Hu Qiongyi, Teng Jialin
Department of Rheumatology and Immunology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Number 197 Ruijin Second Road, Shanghai, 200025, China.
Department of Rheumatology and Immunology, Jiangsu Province Hospital of Traditional Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Clin Rheumatol. 2025 Sep 4. doi: 10.1007/s10067-025-07671-x.
Pulmonary hemorrhage (PH) represents a rare complication in systemic lupus erythematosus (SLE). In this study, we conducted a thorough investigation into the clinical features, diagnosis, treatment modalities, and outcomes of patients with SLE-associated PH at our medical center. Additionally, a comparative analysis of clinical and laboratory parameters before and after rituximab therapy were performed to assess its efficacy in the management of SLE-associated PH.
Seven SLE-associated PH patients received rituximab therapy at Ruijin Hospital from October 2016 to March 2025 were retrospectively reviewed. The clinical manifestations, laboratory tests, chest CT images before and after treatment were recorded.
Among the patients, five were female and two were male, with a median age at diagnosis of 29 years (IQR: 23-64 years). All patients manifested dyspnea, with hemoptysis occurring in 63.5% of cases. The respiratory manifestations of all seven enrolled patients quickly achieved complete recovery and radiographic scan revealed the reduction or complete disappearance of pulmonary infiltrates. The decreased hemoglobin levels quickly rebounded. There was a decrease in the levels of IgG, IgA and IgM concurrently with an increase in C3 and C4. The levels of anti-dsDNA antibodies and positive anti-phospholipid antibodies, SLEDAI-2 K Score showed significant decrease after rituximab treatment. Additionally, the proportion of CD19 and CD20 lymphocytes rapidly reduced after one month of rituximab treatment. The median follow-up duration after rituximab treatment was 23 months (IQR: 17-32 months). All seven patients achieved remission and did not experience a relapse of PH and SLE.
Careful consideration is needed in diagnosing SLE-associated PH in young female patients presenting with dyspnea, severe anemia, and pulmonary infiltration, even in the absence of hemoptysis. Rituximab likely demonstrates effectiveness in treating SLE-associated PH, indicating rituximab should be regarded as an alternative treatment for these patients. Key Points • Pulmonary hemorrhage (PH) is a rare yet severe complication of SLE. The treatment for PH in SLE remains uncertain, and evidence for rituximab use is limited to a few case reports. • This study presents a relatively large patient cohort, demonstrating that rituximab effectively resolves clinical symptoms and improves laboratory parameters. • Rituximab, by targeting B cells, may be a promising therapeutic option for SLE-associated PH.
肺出血(PH)是系统性红斑狼疮(SLE)中一种罕见的并发症。在本研究中,我们对我院SLE相关PH患者的临床特征、诊断、治疗方式及预后进行了深入调查。此外,对利妥昔单抗治疗前后的临床和实验室参数进行了对比分析,以评估其在治疗SLE相关PH中的疗效。
回顾性分析2016年10月至2025年3月在瑞金医院接受利妥昔单抗治疗的7例SLE相关PH患者。记录其临床表现、实验室检查及治疗前后的胸部CT图像。
患者中5例为女性,2例为男性,诊断时的中位年龄为29岁(四分位间距:23 - 64岁)。所有患者均有呼吸困难,63.5%的病例出现咯血。所有7例入选患者的呼吸系统表现迅速完全恢复,影像学扫描显示肺部浸润减少或完全消失。降低的血红蛋白水平迅速回升。IgG、IgA和IgM水平下降,同时C3和C4水平升高。利妥昔单抗治疗后,抗双链DNA抗体水平、抗磷脂抗体阳性率及SLEDAI - 2K评分均显著降低。此外,利妥昔单抗治疗1个月后,CD19和CD20淋巴细胞比例迅速降低。利妥昔单抗治疗后的中位随访时间为23个月(四分位间距:17 - 32个月)。所有7例患者均达到缓解,未出现PH和SLE复发。
对于出现呼吸困难、严重贫血和肺部浸润的年轻女性患者,即使没有咯血,在诊断SLE相关PH时也需要仔细考虑。利妥昔单抗可能对治疗SLE相关PH有效,表明利妥昔单抗应被视为这些患者的替代治疗方法。要点:•肺出血(PH)是SLE罕见但严重的并发症。SLE中PH的治疗仍不确定,利妥昔单抗使用的证据仅限于少数病例报告。•本研究展示了一个相对较大的患者队列,表明利妥昔单抗能有效缓解临床症状并改善实验室参数。•利妥昔单抗通过靶向B细胞,可能是治疗SLE相关PH的一种有前景的治疗选择。