scholarly journals Activation of Tissue Remodeling Precedes Obliterative Bronchiolitis in Lung Transplant Recipients

2008 ◽  
Vol 3 ◽  
pp. BMI.S686 ◽  
Author(s):  
Allan M. Ramirez ◽  
David R. Nunley ◽  
Mauricio Rojas ◽  
Jesse Roman

Obliterative bronchiolitis (OB) and Bronchiolitis Obliterans Syndrome (BOS) are frequent complications in the lung transplant recipient, and are the leading cause of mortality after transplantation. The mechanisms responsible for OB remain elusive, but inflammatory and tissue remodeling responses are implicated. We hypothesized that alterations in markers of tissue remodeling in BALF of lung transplant recipients could predict development of OB. To test this, we identified 13 lung transplant recipients who developed both BOS and histologic OB (OB group) at median post-operative day (POD) 485 (range 73–2070). Bronchoalveolar lavage fluid (BALF) was obtained at median POD 387 (range 45–2205), which preceded the onset of OB and BOS by a median of 140 days (range 60–365). As a control, BALF was also obtained from a group of 21 stable recipients without OB (non-OB group) at median POD 335 (range 270–395). BALF was examined for gelatinolytic activity, fibronectin gene transcription, and transforming growth factor-β1 (TGF-β1) expression. Gelatin zymography of BALF from the OB group showed increased matrix metalloproteinase-9 (MMP-9) activity over that of the non-OB group (p < 0.005). Similarly, BALF from the OB group induced greater fibronectin expression in fibroblasts compared to the non-OB group (p < 0.03). The induction of fibronectin also correlated with the amount of TGF-β1 protein in BALF (r = 0.71) from the OB group. We conclude that activation of tissue remodeling precedes the onset of OB, and analysis of gelatinolytic and/or fibronectin-inducing activity in BALF can serve as an early, pre-clinical marker for OB.

1997 ◽  
Vol 156 (6) ◽  
pp. 1978-1986 ◽  
Author(s):  
CONNIE A. TRELLO ◽  
DEBBIE A. WILLIAMS ◽  
CESAR A. KELLER ◽  
COURTNEY CRIM ◽  
ROBERT O. WEBSTER ◽  
...  

1992 ◽  
Vol 5 ◽  
pp. S242-S245 ◽  
Author(s):  
J. Cerrina ◽  
F. Le Roy Ladurie ◽  
P. H. Herve ◽  
F. Parquin ◽  
S. Harari ◽  
...  

2020 ◽  
Vol 58 (2) ◽  
pp. 379-388
Author(s):  
Anna E Frick ◽  
Stijn E Verleden ◽  
Sofie Ordies ◽  
Annelore Sacreas ◽  
Robin Vos ◽  
...  

Abstract OBJECTIVES Primary graft dysfunction (PGD) remains a major post-transplant complication and is associated with increased morbidity and mortality. Mechanisms evoking PGD are not completely clear, but inflammation plays a central role. We investigated the association between PGD and inflammatory proteins present in immediate postoperative bronchoalveolar lavage. METHODS All double-lung recipients transplanted at our institution from 2002 to 2018 were included in our study. We retrospectively selected 80 consecutive lung transplant recipients with different PGD grades (n = 20 for each PGD grades 0–1 to 2–3). In bronchoalveolar lavage performed within the first 24 h after donor aortic cross-clamping following lung transplantation, concentrations of 30 cytokines, chemokines and growth factors were assessed by enzyme-linked immunosorbent assay (ELISA) and correlated with donor and recipient demographics and outcomes. For analysis, 2 groups were defined: ‘mild’ PGD (grade 0–1) and ‘severe’ PGD (grades 2–3). RESULTS Significant differences between mild and severe PGD were found in 8 biomarkers [interleukin (IL)-6, IL-10, IL-13, eotaxin, granulocyte colony-stimulating factor, interferon γ, macrophage inflammatory protein 1α, surfactant protein D (SP-D); P &lt; 0.05]. Increased IL-10 and IL-13, but none of the other proteins, were associated with short-term outcome (longer time to extubation; P = 0.005 and P &lt; 0.0001; increased intensive care unit stay; P = 0.012 and P &lt; 0.0001; and hospital stay; P = 0.041 and P = 0.002). There were no significant differences in donor and recipient characteristics between the groups. CONCLUSIONS Expression profiles of key inflammatory mediators in bronchoalveolar lavage fluid differed significantly between lung transplant recipients with severe versus mild PGD and correlated with clinical outcome variables. Further research should focus on the early mechanisms leading to PGD.


CHEST Journal ◽  
2007 ◽  
Vol 132 (4) ◽  
pp. 606B
Author(s):  
Binal S. Kancherla ◽  
Marc Schecter ◽  
Haibin Zhang ◽  
John Robertson ◽  
Minh Doan ◽  
...  

2003 ◽  
Vol 3 (6) ◽  
pp. 736-742 ◽  
Author(s):  
Rachel E. Stanford ◽  
Saed Ahmed ◽  
Margaret Hodson ◽  
Nicholas R. Banner ◽  
Marlene L. Rose

2004 ◽  
Vol 190 (6) ◽  
pp. 1076-1083 ◽  
Author(s):  
Glen P. Westall ◽  
Alexandra Michaelides ◽  
Trevor J. Williams ◽  
Greg I. Snell ◽  
Thomas C. Kotsimbos

2002 ◽  
Vol 165 (10) ◽  
pp. 1439-1444 ◽  
Author(s):  
Steven R. Duncan ◽  
Colm Leonard ◽  
James Theodore ◽  
Mark Lega ◽  
Reda E. Girgis ◽  
...  

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