ENHANCEMENT OF CYTOMEGALOVIRUS INFECTION AND ACUTE REJECTION AFTER ALLOGENEIC LUNG TRANSPLANTATION IN THE RAT
- 27 April 1996
- journal article
- immunobiology
- Published by Wolters Kluwer Health in Transplantation
- Vol. 61 (8) , 1250-1260
- https://doi.org/10.1097/00007890-199604270-00022
Abstract
A possible mechanism of the induction of lung transplant rejection by cytomegalovirus (CMV) infection is the inflammatory upregulation of adhesion ligand molecules on transplant endothelia by the viral infection leading to leukocyte activation. To study this question a rat model of rat cytomegalovirus (RCMV) infection and acute lung transplant rejection was established to study: (1) the influence of RCMV infection on the course of rejection, (2) the influence of rejection on the course of RCMV infection, and (3) the influence of RCMV on adhesion molecule expression and leukocyte infiltration. For this Lew (RT1l) rats received either syngenic (n=25) or allogeneic (BN, RT1n; n=38) left lateral lung transplants. Postoperatively, CsA 25mg/kg was given on days 1-3 and triple drug (CsA, Aza, Pred) immunosuppression was given from days 4-10 to induce systemic RCMV infection and acute rejection developed from postoperative day (POD) 15-25 in allogeneic transplants. In RCMV-positive animals the rejection grade was gradually increased at POD 15 and 18. Furthermore, after allogeneic transplantation an enhanced viral infection of the lung transplant as early as POD 11 was found and increased salivary gland PFU titers on days 20 and 25. In the absence of rejection infiltration a maximal induction of ICAM-1 adhesion molecules was found on lung endothelia in RCMV+ allogeneic animals as compared with noninfected controls. This induction was found to lesser degree for VCAM-1 and MHC class II adhesion ligand molecules. This was accompanied by a significantly increased CD11a+ and CD49d+ leukocyte infiltration into the alveolar interstitium on day 11 and 15 in infected transplants. The results show an enhancement of RCMV infection after allogeneic lung transplantation leading to endothelial activation and recruitment of CD11a/CD49d+ leukocytes. This mechanism may strongly influence transplant inflammation and the long-term course of lung transplant rejection.Keywords
This publication has 19 references indexed in Scilit:
- Cytomegalovirus infection enhances smooth muscle cell proliferation and intimal thickening of rat aortic allografts.Journal of Clinical Investigation, 1993
- ARE MULTIPLE IMMUNOPATHOGENETIC EVENTS OCCURRING DURING THE DEVELOPMENT OF OBLITERATIVE BRONCHIOLITIS AND ACUTE REJECTION?Transplantation, 1993
- T LYMPHOCYTE ACTIVATION BY CYTOMEGALOVIRUS-INFECTED, ALLOGENEIC CULTURED HUMAN ENDOTHELIAL CELLSTransplantation, 1992
- DOES HISTOLOGIC ACUTE REJECTION IN LUNG ALLOGRAFTS PREDICT THE DEVELOPMENT OF BRONCHIOLITIS OBLITERANS?Transplantation, 1991
- The Indirect Effects of Cytomegalovirus Infection on the Outcome of Organ TransplantationJAMA, 1989
- The Importance of Cytomegalovirus in Heart-Lung Transplant RecipientsChest, 1989
- The development and characterization of monoclonal antibodies against rat cytomegalovirus induced antigensArchiv für die gesamte Virusforschung, 1987
- Cytomegalovirus infection of rat endothelial cellsin vitroArchiv für die gesamte Virusforschung, 1986
- Biology of Rat Cytomegalovirus InfectionIntervirology, 1985
- Infection of laboratory rats with a new cytomegalo-like virusArchiv für die gesamte Virusforschung, 1983