Epidemiology and persistence of rhinovirus in pediatric lung transplantation.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 23 02 2020
revised: 19 06 2020
accepted: 12 07 2020
pubmed: 21 7 2020
medline: 12 8 2021
entrez: 21 7 2020
Statut: ppublish

Résumé

Infection with rhinovirus (HRV) occurs following pediatric lung transplantation. Prospective studies documenting frequencies, persistence, and progression of HRV in this at-risk population are lacking. In the Clinical Trials in Organ Transplant in Children prospective observational study, we followed 61 lung transplant recipients for 2 years. We quantified molecular subtypes of HRV in serially collected nasopharyngeal (NP) and bronchoalveolar lavage (BAL) samples and correlated them with clinical characteristics. We identified 135 community-acquired respiratory infections (CARV) from 397 BAL and 480 NP samples. We detected 93 HRV events in 42 (68.8%) patients, 22 of which (23.4%) were symptomatic. HRV events were contiguous with different genotypes identified in 23 cases, but symptoms were not preferentially associated with any particular species. Nine (9.7%) HRV events persisted over multiple successive samples for a median of 36 days (range 18-408 days). Three persistent HRV were symptomatic. When we serially measured forced expiratory volume in one second (FEV1) in 23 subjects with events, we did not observe significant decreases in lung function over 12 months post-HRV. In conjunction with our previous reports, our prospectively collected data indicate that molecularly heterogeneous HRV infections occur commonly following pediatric lung transplantation, but these infections do not negatively impact clinical outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Infection with rhinovirus (HRV) occurs following pediatric lung transplantation. Prospective studies documenting frequencies, persistence, and progression of HRV in this at-risk population are lacking.
METHODS METHODS
In the Clinical Trials in Organ Transplant in Children prospective observational study, we followed 61 lung transplant recipients for 2 years. We quantified molecular subtypes of HRV in serially collected nasopharyngeal (NP) and bronchoalveolar lavage (BAL) samples and correlated them with clinical characteristics.
RESULTS RESULTS
We identified 135 community-acquired respiratory infections (CARV) from 397 BAL and 480 NP samples. We detected 93 HRV events in 42 (68.8%) patients, 22 of which (23.4%) were symptomatic. HRV events were contiguous with different genotypes identified in 23 cases, but symptoms were not preferentially associated with any particular species. Nine (9.7%) HRV events persisted over multiple successive samples for a median of 36 days (range 18-408 days). Three persistent HRV were symptomatic. When we serially measured forced expiratory volume in one second (FEV1) in 23 subjects with events, we did not observe significant decreases in lung function over 12 months post-HRV.
CONCLUSION CONCLUSIONS
In conjunction with our previous reports, our prospectively collected data indicate that molecularly heterogeneous HRV infections occur commonly following pediatric lung transplantation, but these infections do not negatively impact clinical outcomes.

Identifiants

pubmed: 32686323
doi: 10.1111/tid.13422
pmc: PMC7900771
mid: NIHMS1627018
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13422

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI077810
Pays : United States

Informations de copyright

© 2020 Wiley Periodicals LLC.

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Auteurs

Evan Ammerman (E)

Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.

Stuart C Sweet (SC)

Washington University in St. Louis, St. Louis, Missouri, USA.

Gregory A Storch (GA)

Washington University in St. Louis, St. Louis, Missouri, USA.

Richard S Buller (RS)

Washington University in St. Louis, St. Louis, Missouri, USA.

Sheila Mason (S)

Washington University in St. Louis, St. Louis, Missouri, USA.

Carol Conrad (C)

Lucile Packard Children's Hospital, Palo Alto, California, USA.

Don Hayes (D)

Nationwide Children's Hospital, Columbus, Ohio, USA.

Albert Faro (A)

Washington University in St. Louis, St. Louis, Missouri, USA.
Cystic Fibrosis Foundation, Bethesda, Maryland, USA.

Samuel B Goldfarb (SB)

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

Ernestina Melicoff (E)

Texas Children's Hospital, Houston, Texas, USA.

Marc Schecter (M)

Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.

Gary Visner (G)

Boston Children's Hospital, Boston, Massachusetts, USA.

Peter S Heeger (PS)

Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Thalachallour Mohanakumar (T)

Norton Thoracic Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.

Nikki Williams (N)

National Institutes of Health, NIAID, Bethesda, Maryland, USA.

Lara Danziger-Isakov (L)

Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.

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