| Literature DB >> 22172867 |
A Mohammed1, O Ulukpo, E C Lawrence, F Fernandez, A Pickens, A A Gal, S D Force, K C Easley, C P Larsen, A D Kirk, D C Neujahr.
Abstract
Outcomes following lung transplant remain suboptimal. This is attributable to variable posttransplant recovery of lung function, and inconsistent degrees of lung function loss after peak function is reached. Granzyme B is elevated in the blood and bronchoalveolar lavage (BAL) in acute rejection. We hypothesized that persistent exposure to T cells high in granzyme B would negatively correlate with lung function. We investigated cumulative exposure measured as the area-under-the-curve (AUC) of CD8+ T cell granzyme Bhi cells in the first year posttransplant in both BAL and blood in 24 transplant recipients. We assessed the correlation between cumulative 1-year exposure and FEV1 slope. There was a negative correlation between 1-year exposure and FEV1 slope within the first year (r=-0.63; P=.001). This relationship persisted even when adjusted for transplant type, gender, age, rejection, and indication for transplantation. In contrast, no relationship was seen with the 1-year AUC and lung function after 1 year posttransplant. In contrast to the BAL granzyme Bhi levels, granzyme Bhi levels from the blood showed no relationship with lung function. These findings suggest that CD8+ T-cell-driven factors are responsible for early improvements in lung function after transplantation.Entities:
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Year: 2011 PMID: 22172867 PMCID: PMC3395055 DOI: 10.1016/j.transproceed.2011.09.072
Source DB: PubMed Journal: Transplant Proc ISSN: 0041-1345 Impact factor: 1.066