1. THE USE OF GRANZYME A AS A MARKER OF HEART TRANSPLANT REJECTION IN CYCLOSPORINE OR ANTI-CD4 MONOCLONAL ANTIBODY-TREATED RATS
- Author
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C G Fathman, Gillian M. Griffiths, Vaughn A. Starnes, Flavin Tf, Irving L. Weissman, Rong Chen, Margaret E. Billingham, Judith A. Shizuru, Ivens K, and Susan Alpert
- Subjects
Graft Rejection ,Male ,Pathology ,medicine.medical_specialty ,medicine.drug_class ,medicine.medical_treatment ,CD4-CD8 Ratio ,In situ hybridization ,Biology ,Monoclonal antibody ,Granzymes ,medicine ,Animals ,Transplantation, Homologous ,Cytotoxic T cell ,Transplantation ,Graft Survival ,Serine Endopeptidases ,Antibodies, Monoclonal ,Immunotherapy ,Rats ,Rats, Inbred ACI ,Transplantation, Isogeneic ,Rats, Inbred Lew ,Histocompatibility ,CD4 Antigens ,Immunology ,Cyclosporine ,Granzyme A ,Heart Transplantation ,Immunohistochemistry ,Biomarkers ,CD8 ,T-Lymphocytes, Cytotoxic - Abstract
Granzyme A is a serine protease expressed by populations of human and mouse natural killer cells and activated CD4+ and CD8+ cytotoxic lymphocytes; its expression marks a subset of inflammatory cells in allografts, autoimmune diabetes, and a number of other inflammatory lesions. In order to describe more completely the correlation between granzyme A expression and the presence of in vivo cytolytic effects, we grafted allogeneic rat hearts with vascular anastomoses in a heterotopic location, and treated the hosts with either cyclosporine, anti-CD4 monoclonal antibody (MRC OX38), or no therapy. The grafts were evaluated by palpation for cardiac functions, by immunohistochemistry for CD4/CD8 expression, by hematoxylin-and-eosin staining for inflammatory infiltration, and by in situ hybridization for granzyme A expression. The appearance of granzyme A+ cells in untreated allografts preceded both functional and standard histopathological and immunohistochemical evidence of graft rejection by two days. In donor-recipient combinations where cyclosporine and anti-CD4 treatments allowed indefinite allograft survival, the allografts showed minimal numbers of granzyme A+ cells, whether cellular infiltrates developed or not. The number of granzyme A+ cells present in the cardiac allografts in treated and untreated animals correlated with either current or impending episodes of rejection. The early time course of granzyme A expression suggests that it can be used as an early and reliable marker of graft rejection.
- Published
- 1993