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1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality

BACKGROUND: Human rhinovirus (HRV) lower respiratory tract infection (LRTI) is associated with significant mortality in hematopoietic cell transplant (HCT) recipients. The associations between specific cytokine responses and mortality after HRV LRTI are not known. METHODS: Stored frozen BALF samples...

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Autores principales: Waghmare, Alpana, Jenkins, Isaac, Edmison, Brad, Loeffelholz, Tillie, Stevens-Ayers, Terry, Greninger, Alex, Kuypers, Jane, Jerome, Keith, Englund, Janet, Leisenring, Wendy, Boeckh, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253112/
http://dx.doi.org/10.1093/ofid/ofy209.140
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author Waghmare, Alpana
Jenkins, Isaac
Edmison, Brad
Loeffelholz, Tillie
Stevens-Ayers, Terry
Greninger, Alex
Kuypers, Jane
Jerome, Keith
Englund, Janet
Leisenring, Wendy
Boeckh, Michael
author_facet Waghmare, Alpana
Jenkins, Isaac
Edmison, Brad
Loeffelholz, Tillie
Stevens-Ayers, Terry
Greninger, Alex
Kuypers, Jane
Jerome, Keith
Englund, Janet
Leisenring, Wendy
Boeckh, Michael
author_sort Waghmare, Alpana
collection PubMed
description BACKGROUND: Human rhinovirus (HRV) lower respiratory tract infection (LRTI) is associated with significant mortality in hematopoietic cell transplant (HCT) recipients. The associations between specific cytokine responses and mortality after HRV LRTI are not known. METHODS: Stored frozen BALF samples from adult and pediatric HCT recipients with HRV detected in BALF were analyzed for 30 cytokines (Mesoscale, Rockville, MD). An elasticnet model with Cox regression was used to identify cytokines and other covariates most associated with overall and pulmonary mortality at 90 days, including cytopenias, baseline oxygen (O(2)) use, copathogens, steroid use, viral load, and viral species. Identified variables were evaluated in multivariable models and the impact of each variable on the bootstrapped optimism corrected concordance statistic (c-statistic) was calculated. Cytokine levels as outcomes were evaluated using multivariable linear regression. RESULTS: BALF from 84 HCT recipients with HRV detected in BALF from 1998 to 2015 were included in the analysis. Variables identified in the elasticnet model included: baseline O(2), monocyte count, lymphocyte count, steroid use, endothelial neutrophil activator 78 (ENA-78), IL-4, IL-15, IFN-a2a, and MCP-2. Viral load and species were not associated with mortality. In the model with the highest c-statistic, baseline O(2), monocyte count, lymphocyte count, steroid use, and ENA-78 [adjusted hazard ratio (aHR) 1.19, 95% confidence interval (CI) 1.05–1.35] were significantly associated with overall mortality. For pulmonary mortality, the same clinical factors (except for steroids) and IL-4 (aHR 1.27, 95% CI 1.06–1.54) were associated with the outcome (Figure 1). Models including multiple cytokines did not improve the c-statistic. IL-4 levels were associated with viral load but not with host or clinical factors (slope 0.36, 95% CI 0.1–0.61) (Figure 2). CONCLUSION: Elevated IL-4 levels in BALF of HCT recipients with HRV LRTI were associated with increased risk of day 90 pulmonary mortality and may provide unique prognostic information. Viral load and species were not associated with mortality, suggesting that host immune responses play a larger role than viral factors in disease severity. Cytokines may be possible targets for intervention. [Image: see text] [Image: see text] DISCLOSURES: A. Waghmare, Ablynx: Investigator, Research support. J. Englund, Gilead: Consultant and Investigator, Consulting fee and Research support. Novavax: Investigator, Research support. GlaxoSmithKline: Investigator, Research support. Alios: Investigator, Research support. MedImmune: Investigator, Research support. M. Boeckh, Asun Biopharma: Consultant and Investigator, Consulting fee and Research support. Gilead Sciences: Consultant and Investigator, Consulting fee and Research support. Chimerix Inc.: Consultant and Investigator, Consulting fee and Research support. Humabs: Consultant, Consulting fee. GSK: Investigator, Research support.
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spelling pubmed-62531122018-11-28 1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality Waghmare, Alpana Jenkins, Isaac Edmison, Brad Loeffelholz, Tillie Stevens-Ayers, Terry Greninger, Alex Kuypers, Jane Jerome, Keith Englund, Janet Leisenring, Wendy Boeckh, Michael Open Forum Infect Dis Abstracts BACKGROUND: Human rhinovirus (HRV) lower respiratory tract infection (LRTI) is associated with significant mortality in hematopoietic cell transplant (HCT) recipients. The associations between specific cytokine responses and mortality after HRV LRTI are not known. METHODS: Stored frozen BALF samples from adult and pediatric HCT recipients with HRV detected in BALF were analyzed for 30 cytokines (Mesoscale, Rockville, MD). An elasticnet model with Cox regression was used to identify cytokines and other covariates most associated with overall and pulmonary mortality at 90 days, including cytopenias, baseline oxygen (O(2)) use, copathogens, steroid use, viral load, and viral species. Identified variables were evaluated in multivariable models and the impact of each variable on the bootstrapped optimism corrected concordance statistic (c-statistic) was calculated. Cytokine levels as outcomes were evaluated using multivariable linear regression. RESULTS: BALF from 84 HCT recipients with HRV detected in BALF from 1998 to 2015 were included in the analysis. Variables identified in the elasticnet model included: baseline O(2), monocyte count, lymphocyte count, steroid use, endothelial neutrophil activator 78 (ENA-78), IL-4, IL-15, IFN-a2a, and MCP-2. Viral load and species were not associated with mortality. In the model with the highest c-statistic, baseline O(2), monocyte count, lymphocyte count, steroid use, and ENA-78 [adjusted hazard ratio (aHR) 1.19, 95% confidence interval (CI) 1.05–1.35] were significantly associated with overall mortality. For pulmonary mortality, the same clinical factors (except for steroids) and IL-4 (aHR 1.27, 95% CI 1.06–1.54) were associated with the outcome (Figure 1). Models including multiple cytokines did not improve the c-statistic. IL-4 levels were associated with viral load but not with host or clinical factors (slope 0.36, 95% CI 0.1–0.61) (Figure 2). CONCLUSION: Elevated IL-4 levels in BALF of HCT recipients with HRV LRTI were associated with increased risk of day 90 pulmonary mortality and may provide unique prognostic information. Viral load and species were not associated with mortality, suggesting that host immune responses play a larger role than viral factors in disease severity. Cytokines may be possible targets for intervention. [Image: see text] [Image: see text] DISCLOSURES: A. Waghmare, Ablynx: Investigator, Research support. J. Englund, Gilead: Consultant and Investigator, Consulting fee and Research support. Novavax: Investigator, Research support. GlaxoSmithKline: Investigator, Research support. Alios: Investigator, Research support. MedImmune: Investigator, Research support. M. Boeckh, Asun Biopharma: Consultant and Investigator, Consulting fee and Research support. Gilead Sciences: Consultant and Investigator, Consulting fee and Research support. Chimerix Inc.: Consultant and Investigator, Consulting fee and Research support. Humabs: Consultant, Consulting fee. GSK: Investigator, Research support. Oxford University Press 2018-11-26 /pmc/articles/PMC6253112/ http://dx.doi.org/10.1093/ofid/ofy209.140 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Waghmare, Alpana
Jenkins, Isaac
Edmison, Brad
Loeffelholz, Tillie
Stevens-Ayers, Terry
Greninger, Alex
Kuypers, Jane
Jerome, Keith
Englund, Janet
Leisenring, Wendy
Boeckh, Michael
1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality
title 1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality
title_full 1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality
title_fullStr 1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality
title_full_unstemmed 1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality
title_short 1734. Cytokine Levels in Bronchoalveolar Lavage Fluid of Rhinovirus-Infected Hematopoietic Cell Transplant Recipients: Associations With Mortality
title_sort 1734. cytokine levels in bronchoalveolar lavage fluid of rhinovirus-infected hematopoietic cell transplant recipients: associations with mortality
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253112/
http://dx.doi.org/10.1093/ofid/ofy209.140
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