Piñana José Luis, Carbonell-Asins Juan A, Gómez Dolores, Montoro Juan, Pérez Ariadna, Hernani Rafael, Chorão Pedro, Hernández-Boluda Juan Carlos, Navarro David, Solano Carlos
Department of Hematology, Hospital Clínico Universitario of Valencia, Spain.
INCLIVA, Biomedical Research Institute, Valencia, Spain.
Clin Infect Dis. 2025 Oct 6;81(3):570-580. doi: 10.1093/cid/ciae602.
Studies on late community-acquired respiratory virus (CARV) infections in long-term allogeneic hematopoietic stem cell transplantation (allo-HCT) survivors are scarce, creating knowledge gaps on the epidemiology, risk of progression to lower respiratory tract disease (LRTD), and conditions linked to poor outcomes.
We included consecutive CARV infection episodes occurring up to 6 months after allo-HCT registered in our database from December 2013 to June 2023 at 2 Spanish transplant centers.
Among 426 allo-HCT recipients, 1070 CARV episodes were recorded, 791 (74%) with only upper respiratory tract disease (URTD) and 279 (15%) progressing to LRTD, at a median of 18.6 months post-transplant. The most common CARVs were rhinovirus, respiratory syncytial virus (RSV), and influenza. The LRTD progression rate was 26%, with a 4.9% all-cause mortality rate at 100 days post-CARV detection. Risk factors for LRTD progression included graft-versus-host disease prophylaxis (odds ratio [OR] 3.08), corticosteroid use (0.1 to <30 mg/day: OR 2.44; ≥30 mg/day: OR 5.19), absolute lymphocyte count (ALC) <1 × 10^9/L (OR 1.60), fever at CARV screening (OR 4.27), RSV (OR 2.46), and human metapneumovirus (HMPV) (OR 2.76). Risk factors for 100-day all-cause mortality included human leukocyte antigen (HLA) mismatch (hazard ratio [HR] 2.49); corticosteroid use (0.1 to <30 mg/day: HR 3.87; ≥30 mg/day: HR 5.77); ALC <1 × 10^9/L (HR 2.44); neutropenia <0.5 × 10^9/L (HR 6.74), and age ≥40 years (HR 4.85).
Recipients with profound and prolonged immunosuppression remain at risk for severe CARV infection outcomes late after allo-HCT, necessitating intensive clinical monitoring for respiratory symptoms.
关于长期异基因造血干细胞移植(allo-HCT)幸存者中晚期社区获得性呼吸道病毒(CARV)感染的研究较少,这在流行病学、进展为下呼吸道疾病(LRTD)的风险以及与不良结局相关的情况方面造成了知识空白。
我们纳入了2013年12月至2023年6月在西班牙2个移植中心登记的、在allo-HCT后6个月内发生的连续性CARV感染病例。
在426例allo-HCT受者中,记录到1070次CARV感染发作,其中791次(74%)仅为上呼吸道疾病(URTD),279次(15%)进展为LRTD,移植后中位时间为18.6个月。最常见的CARV是鼻病毒、呼吸道合胞病毒(RSV)和流感病毒。LRTD进展率为26%,在CARV检测后100天的全因死亡率为4.9%。LRTD进展的危险因素包括移植物抗宿主病预防(比值比[OR] 3.08)、使用皮质类固醇(0.1至<30 mg/天:OR 2.44;≥30 mg/天:OR 5.19)、绝对淋巴细胞计数(ALC)<1×10^9/L(OR 1.60)、CARV筛查时发热(OR 4.27)、RSV(OR 2.46)和人偏肺病毒(HMPV)(OR 2.76)。100天全因死亡率的危险因素包括人类白细胞抗原(HLA)不匹配(风险比[HR] 2.49);使用皮质类固醇(0.1至<30 mg/天:HR 3.87;≥30 mg/天:HR 5.77);ALC <1×10^9/L(HR 2.44);中性粒细胞减少<0.5×10^9/L(HR 6.74),以及年龄≥40岁(HR 4.85)。
免疫抑制严重且持续时间长的受者在allo-HCT后期仍有发生严重CARV感染结局的风险,因此需要对呼吸道症状进行强化临床监测。