Immunologic factors in transplant arteriopathy: insight from animal models
- PMID: 12764538
Immunologic factors in transplant arteriopathy: insight from animal models
Abstract
Transplant arteriopathy is the leading cause of long-term morbidity and mortality following heart transplantation. The pathologic hallmark of this disease is intimal proliferation. Animal models have demonstrated that immunologic factors, including cytokines, cellular adhesion molecules and inflammatory cells, play a significant role in the development of this arteriopathy. One goal of future studies will be to translate findings in animal models into effective treatments in humans.
Similar articles
-
Inhibition of MCP-1/CCR2 signaling does not inhibit intimal proliferation in a mouse aortic transplant model.J Vasc Res. 2008;45(6):538-46. doi: 10.1159/000129688. Epub 2008 May 7. J Vasc Res. 2008. PMID: 18463419
-
Coronary arteriopathy postcardiac transplant in a heterotopic piglet model: the role of matrix-cytokine interaction.Transplant Proc. 1993 Feb;25(1 Pt 2):859-60. Transplant Proc. 1993. PMID: 8442248 No abstract available.
-
Increased interleukin-1 beta and fibronectin expression are early features of the development of the postcardiac transplant coronary arteriopathy in piglets.Am J Pathol. 1993 Jun;142(6):1772-86. Am J Pathol. 1993. PMID: 8506947 Free PMC article.
-
Cellular adhesion molecules in transplantation.Transplant Proc. 1996 Dec;28(6):3285-9. Transplant Proc. 1996. PMID: 8962274 Review. No abstract available.
-
Alloreactivity as therapeutic principle in the treatment of hematologic malignancies. Studies of clinical and immunologic aspects of allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning.Dan Med Bull. 2007 May;54(2):112-39. Dan Med Bull. 2007. PMID: 17521527 Review.
Cited by
-
Cardiac allograft vasculopathy: the Achilles' heel of long-term survival after cardiac transplantation.Curr Atheroscler Rep. 2006 Mar;8(2):119-30. doi: 10.1007/s11883-006-0049-1. Curr Atheroscler Rep. 2006. PMID: 16510046 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical