Clinical characteristics and outcomes of viral respiratory infections in allogeneic haematopoietic stem cell transplantation recipients: a single-centre experience.

Clinical characteristics and outcomes of viral respiratory infections in allogeneic haematopoietic stem cell transplantation recipients: a single-centre experience.

Publication date: Sep 01, 2025

Introduction. Allogeneic haematopoietic stem cell transplantation (allo-HSCT) is a treatment option for haematological malignancies. Allo-HSCT patients are more susceptible to viral infections due to immunosuppression. Gap Statement. The bone marrow transplant programme in Qatar, established within the past decade, remains in a developmental phase. A thorough evaluation of infection-related outcomes is essential to identify areas for improvement and to enhance infection control measures. Aim. This study aims to estimate the incidence, clinical impact and outcomes of viral respiratory tract infection (vRTI) in allo-HSCT recipients. Methodology. A total of 64 allo-HSCT patients were included in this study. Respiratory samples were collected from patients presenting with respiratory symptoms or during episodes of febrile neutropenia without an identified source. Nasopharyngeal swabs were the primary sampling method for upper respiratory tract infections (URTIs), while sputum, bronchoalveolar lavage or tracheal aspirates were obtained in patients with lower respiratory tract involvement or those requiring mechanical ventilation. During the high-risk COVID-19 pandemic period, pre-admission screening for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was routinely performed for all patients undergoing transplantation or chemotherapy. All samples were assessed using multiplex PCR assays. Viral agents, outcomes of vRTI occurring in the period of 1 year after allo-HSCT, clinical symptoms, infection-related complications and risk factors were reviewed. Result. A total of 64 allo-HSCT patients were reviewed; 41 of them (53%) had vRTI. SARS-CoV-2, respiratory syncytial virus (RSV), rhinovirus, influenza and parainfluenza were the most common viruses. Importantly, 19 patients (46. 3%) had URTI, and 22 patients (53. 7%) progressed to pneumonia. The risk of vRTI was significantly related to non-corticosteroid immune suppressants (P≤0. 01) and to lymphopenia (P≤0. 05). RSV (66. 7%), coronaviruses (229E, NL63, OC43 and HKU1) (60%) and rhinovirus (58. 3%) were the most dominant viruses associated with the development of pneumonia. Thirteen patients (20. 3%) were admitted to the ICU; eight of them were associated with vRTI (61. 5%). Ten deaths were reported (15. 6%); vRTI was the primary cause of death in one of the deceased patients. Conclusion. Early detection and intervention strategies are crucial in mitigating the impact of these infections. The immune alteration effect of prophylaxis immune suppressants and antiviral therapy exacerbates the risk of infections among allo-HSCT patients. Novel antiviral approaches based on enhancing antiviral immune responses, vaccines and non-pharmaceutical preventive strategies are required to improve outcomes in allo-HSCT patients.

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Concepts Keywords
22patients Adolescent
Bone Adult
Coronaviruses Aged
Haematopoietic COVID-19
Pcr Female
Humans
immunocompromised patients
Incidence
Male
Middle Aged
prophylaxis treatment
Qatar
Respiratory Tract Infections
risk factors
SARS-CoV-2
Transplantation, Homologous
Virus Diseases
Young Adult

Semantics

Type Source Name
disease MESH respiratory infections
disease IDO cell
disease MESH malignancies
disease MESH viral infections
disease IDO immunosuppression
disease MESH infection
disease MESH febrile neutropenia
disease MESH COVID-19 pandemic
disease MESH complications
disease MESH influenza
disease MESH parainfluenza
disease MESH pneumonia
disease MESH lymphopenia
drug DRUGBANK Pentaerythritol tetranitrate
disease MESH cause of death
disease IDO intervention
disease MESH viral shedding
disease MESH morbidity
disease MESH severe acute respiratory syndrome
disease MESH death
disease MESH immunocompromised patients
drug DRUGBANK Dimercaprol
disease MESH graft versus host disease
drug DRUGBANK Medical air
disease MESH invasive fungal infections
drug DRUGBANK Immune Globulin Human
disease IDO blood
disease IDO susceptibility
disease IDO pathogen
drug DRUGBANK Tropicamide
disease IDO host
disease MESH breathlessness
disease MESH hypoxia
disease MESH neutropenia
disease MESH respiratory failure
disease IDO facility
disease IDO symptom
drug DRUGBANK Etoperidone
disease MESH sore throat
disease MESH Lymphoma
drug DRUGBANK Ethanol
drug DRUGBANK Water
pathway KEGG Influenza A
drug DRUGBANK Oseltamivir
drug DRUGBANK Ribavirin
drug DRUGBANK Favipiravir
drug DRUGBANK Trestolone
disease MESH T cell lymphoma
disease MESH bacterial infections
disease MESH aspergillosis
disease MESH relapse
disease IDO country
disease MESH RSV infections
disease MESH fungal infections
drug DRUGBANK Ganciclovir
disease MESH clinical significance
disease MESH pulmonary aspergillosis
disease MESH superinfections
disease MESH critical illness
disease MESH infection transmission
disease MESH hematologic malignancies
disease MESH Infectious Diseases
disease MESH Viral pneumonia
disease MESH retinitis

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