Zhang Zilu, Huang Jingtao, Wang Luxiang, Pan Zengkai, Huang Jiayu, Jiang Chuanhe, Zhang Sujiang, Li Su, Hu Xiaoxia
National Research Center for Translational Medicine, State Key Laboratory of Medical Genomics, Shanghai Institute of Hematology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai 200025, China.
GoBroad Medical Institute of Hematology (Shanghai Center), Shanghai 201418, China.
Blood Sci. 2024 Jan 25;6(2):e00183. doi: 10.1097/BS9.0000000000000183. eCollection 2024 Apr.
Data on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in patients at early stage of immune reconstitution after hematopoietic stem cell transplantation (HSCT) are limited. In the present study, we retrospectively investigated the incidence and clinical features of SARS-CoV-2 infection in patients who underwent HSCT in 2022. Patients (allo-HSCT, n = 80; auto-HSCT, n = 37) were consecutively included in the study. The SARS-CoV-2 infection rate was 59.8%, and the median interval of HSCT to coronavirus disease 2019 (COVID-19) was 4.8 (range: 0.5-12) months. Most patients were categorized as mild (41.4%) or moderate (38.6%), and 20% as severe/critical. No deaths were attributable to COVID-19. Further analysis showed that lower circulating CD8 T-cell counts and calcineurin inhibitor administration increased the risk of SARS-CoV-2 infection. Exposure to rituximab significantly increased the probability of severe or critical COVID-19 compared with that of mild/moderate illness ( < .001). In the multivariate analysis, rituximab use was associated with severe COVID-19. Additionally, COVID-19 had no significant effect on immune reconstitution. Furthermore, it was found that Epstein-Barr virus infection and rituximab administration possibly increase the risk of developing severe illness. Our study provides preliminary insights into the effect of SARS-CoV-2 on immune reconstitution and the outcomes of allo-HSCT recipients.
造血干细胞移植(HSCT)后免疫重建早期患者感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的数据有限。在本研究中,我们回顾性调查了2022年接受HSCT的患者中SARS-CoV-2感染的发生率和临床特征。患者(异基因HSCT,n = 80;自体HSCT,n = 37)连续纳入研究。SARS-CoV-2感染率为59.8%,HSCT至2019冠状病毒病(COVID-19)的中位间隔时间为4.8(范围:0.5 - 12)个月。大多数患者被分类为轻症(41.4%)或中症(38.6%),20%为重症/危重症。没有死亡归因于COVID-19。进一步分析表明,循环CD8 T细胞计数较低和使用钙调神经磷酸酶抑制剂会增加SARS-CoV-2感染的风险。与轻症/中症疾病相比,使用利妥昔单抗显著增加了重症或危重症COVID-19的概率(<0.001)。在多变量分析中,使用利妥昔单抗与重症COVID-19相关。此外,COVID-19对免疫重建没有显著影响。此外,发现爱泼斯坦-巴尔病毒感染和使用利妥昔单抗可能会增加发生重症疾病的风险。我们的研究为SARS-CoV-2对免疫重建的影响以及异基因HSCT受者的结局提供了初步见解。