Human Metapneumovirus Infections Following Hematopoietic Cell Transplantation: Factors Associated With Disease Progression

• Published in: Clinical Infectious Diseases 2016-07, Vol.63 (2), p.178-185
• Main Authors: Seo, Sachiko, Gooley, Ted A., Kuypers, Jane M., Stednick, Zachary, Jerome, Keith R., Englund, Janet A., Boeckh, Michael
• Format: Article
• Language: English
• Subjects: Adrenal Cortex Hormones - administration & dosage; Adult; and Commentaries; ARTICLES AND COMMENTARIES; Cells; Cohort Studies; Disease Progression; Female; Hematopoietic Stem Cell Transplantation - adverse effects; Human metapneumovirus; Humans; Lymphocyte Count; Male; Metapneumovirus; Middle Aged; Paramyxoviridae Infections - physiopathology; Paramyxoviridae Infections - transmission; Pathogenesis; Polymerase chain reaction; Respiratory Tract Infections - physiopathology; Respiratory Tract Infections - transmission; Respiratory Tract Infections - virology; Retrospective Studies; Risk Assessment; Seasons; Transplants & implants; Viral infections; Virus Shedding; Young Adult
• ISSN: 1058-4838; 1537-6591
• DOI: 10.1093/cid/ciw284

Background. Human metapneumovirus (HMPV) is a newly identified pulmonary pathogen that can cause fatal lower respiratory tract disease (LRD) in hematopoietic cell transplantation (HCT) recipients. Little is known about progression rates from upper respiratory tract infection (URI) to LRD and risk factors associated with progression. Methods. A total of 118 HCT recipients receiving transplantation between 2004 and 2014 who had HMPV detected in nasopharyngeal, bronchoalveolar lavage, or lung biopsy samples by real-time reverse transcription polymerase chain reaction were retrospectively analyzed. Results. More than 90% of the cases were identified between December and May. Among the 118 HCT patients, 88 and 30 had URI alone and LRD, respectively. Among 30 patients with LRD, 17 patients progressed from URI to LRD after a median of 7 days (range, 2–63 days). The probability of progression to LRD within 40 days after URI was 16%. In Cox regression analysis, steroid use ≥1 mg/kg prior to URI diagnosis (hazard ratio [HR], 5.10; P = .004), low lymphocyte count (HR, 3.43; P = .011), and early onset of HMPV infection after HCT (before day 30 after HCT; HR, 3.54; P= .013) were associated with higher progression to LRD. The median viral load in nasal wash samples was 1.1 × 106 copies/mL (range, 3.3 × 102 –1.7 × 109) with no correlation between the viral load and progression. Conclusions. Progression from URI to LRD occurred in up to 60% of HCT recipients with risk factors such as systemic corticosteroid use or low lymphocyte counts. Further studies are needed to define the role of viral load in the pathogenesis of progressive disease.