Intragraft Hyaluronan Increases in Association With Acute Lung Transplant Rejection

Background. Acute perivascular rejection (AR) is common in lung recipients and increases the risk for chronic lung allograft dysfunction (CLAD). Hyaluronan (HA), an extracellular matrix constituent, accumulates in experimental AR and can act as an innate immune agonist, breaking tolerance and potent...

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Main Authors: Haley P. Hostetler, MD, Megan L. Neely, PhD, Francine L. Kelly, PhD, John A. Belperio, MD, Marie Budev, MD, John M. Reynolds, MD, Pali D. Shah, MD, Lianne G. Singer, MD, Laurie D. Snyder, MD, Scott M. Palmer, MD, Jamie L. Todd, MD
Format: Article
Language:English
Published: Wolters Kluwer 2021-04-01
Series:Transplantation Direct
Online Access:http://journals.lww.com/transplantationdirect/fulltext/10.1097/TXD.0000000000001138
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spelling doaj-3b098b2da3884d7388c248de3f4d8d782021-09-28T10:22:09ZengWolters KluwerTransplantation Direct2373-87312021-04-0174e68510.1097/TXD.0000000000001138202104000-00008Intragraft Hyaluronan Increases in Association With Acute Lung Transplant RejectionHaley P. Hostetler, MD0Megan L. Neely, PhD1Francine L. Kelly, PhD2John A. Belperio, MD3Marie Budev, MD4John M. Reynolds, MD5Pali D. Shah, MD6Lianne G. Singer, MD7Laurie D. Snyder, MD8Scott M. Palmer, MD9Jamie L. Todd, MD101 Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University Medical Center, Durham, NC.2 Department of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, NC.1 Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University Medical Center, Durham, NC.4 Department of Medicine, University of California Los Angeles, Los Angeles, CA.5 Department of Pulmonary Medicine, Cleveland Clinic, Cleveland, OH.1 Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University Medical Center, Durham, NC.6 Department of Medicine, Johns Hopkins University, Baltimore, MD.7 Department of Medicine, Toronto Lung Transplant Program, University Health Network, University of Toronto, Toronto, ON, Canada.1 Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University Medical Center, Durham, NC.1 Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University Medical Center, Durham, NC.1 Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University Medical Center, Durham, NC.Background. Acute perivascular rejection (AR) is common in lung recipients and increases the risk for chronic lung allograft dysfunction (CLAD). Hyaluronan (HA), an extracellular matrix constituent, accumulates in experimental AR and can act as an innate immune agonist, breaking tolerance and potentiating alloimmunity. We previously demonstrated HA accumulates in CLAD after human-lung transplantation. We sought to determine if HA accumulates in the bronchoalveolar lavage fluid (BALF) concurrent with AR in lung recipients. Methods. The cohort consisted of 126 first adult lung recipients at 5 transplant centers with a total of 373 BALF samples collected within the first posttransplant year. All samples were paired with a lung biopsy from the same bronchoscopy. BALF HA (ng/mL) was quantified by ELISA and log-transformed for analysis. Linear-mixed effect models, adjusted for potential confounders, were used to estimate the association between BALF HA concentration and the presence of AR on biopsy. The association between early posttransplant BALF HA levels and the development of CLAD was explored utilizing tertiles of maximum BALF HA level observed within the first 6 months of transplant. Results. In analyses adjusted for potential confounders, BALF HA concentration was significantly increased in association with AR (change in means on log-scale 0.31; 95% CI, 0.01-0.60; P = 0.044). When considered on the original scale (ng/mL), BALF HA concentrations were 1.36 times (36%) higher, on average, among samples with, versus without, AR. The cumulative incidence of CLAD was numerically higher in individuals in the highest tertiles of BALF HA level within the first 6 months after transplant, as compared with those in the lowest tertile; however, this difference was not statistically significant (P = 0.32). Conclusions. These results demonstrate accumulation of HA in clinical AR and suggest a mechanism by which innate and adaptive immune activation might interact in the development of AR and CLAD.http://journals.lww.com/transplantationdirect/fulltext/10.1097/TXD.0000000000001138
collection DOAJ
language English
format Article
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author Haley P. Hostetler, MD
Megan L. Neely, PhD
Francine L. Kelly, PhD
John A. Belperio, MD
Marie Budev, MD
John M. Reynolds, MD
Pali D. Shah, MD
Lianne G. Singer, MD
Laurie D. Snyder, MD
Scott M. Palmer, MD
Jamie L. Todd, MD
spellingShingle Haley P. Hostetler, MD
Megan L. Neely, PhD
Francine L. Kelly, PhD
John A. Belperio, MD
Marie Budev, MD
John M. Reynolds, MD
Pali D. Shah, MD
Lianne G. Singer, MD
Laurie D. Snyder, MD
Scott M. Palmer, MD
Jamie L. Todd, MD
Intragraft Hyaluronan Increases in Association With Acute Lung Transplant Rejection
Transplantation Direct
author_facet Haley P. Hostetler, MD
Megan L. Neely, PhD
Francine L. Kelly, PhD
John A. Belperio, MD
Marie Budev, MD
John M. Reynolds, MD
Pali D. Shah, MD
Lianne G. Singer, MD
Laurie D. Snyder, MD
Scott M. Palmer, MD
Jamie L. Todd, MD
author_sort Haley P. Hostetler, MD
title Intragraft Hyaluronan Increases in Association With Acute Lung Transplant Rejection
title_short Intragraft Hyaluronan Increases in Association With Acute Lung Transplant Rejection
title_full Intragraft Hyaluronan Increases in Association With Acute Lung Transplant Rejection
title_fullStr Intragraft Hyaluronan Increases in Association With Acute Lung Transplant Rejection
title_full_unstemmed Intragraft Hyaluronan Increases in Association With Acute Lung Transplant Rejection
title_sort intragraft hyaluronan increases in association with acute lung transplant rejection
publisher Wolters Kluwer
series Transplantation Direct
issn 2373-8731
publishDate 2021-04-01
description Background. Acute perivascular rejection (AR) is common in lung recipients and increases the risk for chronic lung allograft dysfunction (CLAD). Hyaluronan (HA), an extracellular matrix constituent, accumulates in experimental AR and can act as an innate immune agonist, breaking tolerance and potentiating alloimmunity. We previously demonstrated HA accumulates in CLAD after human-lung transplantation. We sought to determine if HA accumulates in the bronchoalveolar lavage fluid (BALF) concurrent with AR in lung recipients. Methods. The cohort consisted of 126 first adult lung recipients at 5 transplant centers with a total of 373 BALF samples collected within the first posttransplant year. All samples were paired with a lung biopsy from the same bronchoscopy. BALF HA (ng/mL) was quantified by ELISA and log-transformed for analysis. Linear-mixed effect models, adjusted for potential confounders, were used to estimate the association between BALF HA concentration and the presence of AR on biopsy. The association between early posttransplant BALF HA levels and the development of CLAD was explored utilizing tertiles of maximum BALF HA level observed within the first 6 months of transplant. Results. In analyses adjusted for potential confounders, BALF HA concentration was significantly increased in association with AR (change in means on log-scale 0.31; 95% CI, 0.01-0.60; P = 0.044). When considered on the original scale (ng/mL), BALF HA concentrations were 1.36 times (36%) higher, on average, among samples with, versus without, AR. The cumulative incidence of CLAD was numerically higher in individuals in the highest tertiles of BALF HA level within the first 6 months after transplant, as compared with those in the lowest tertile; however, this difference was not statistically significant (P = 0.32). Conclusions. These results demonstrate accumulation of HA in clinical AR and suggest a mechanism by which innate and adaptive immune activation might interact in the development of AR and CLAD.
url http://journals.lww.com/transplantationdirect/fulltext/10.1097/TXD.0000000000001138
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