Fas ligand-deficient gld mice are more susceptible to graft-versus-host-disease.

Abstract

BACKGROUND:

The Fas/Fas ligand (FasL) pathway plays an important role in a number of apoptotic processes that could be important for the development of graft-versus-host disease (GVHD) after bone marrow transplantation (BMT), such as cytolysis of target cells by cytotoxic T cells, regulation of inflammatory responses, peripheral deletion of autoimmune cells, costimulation of T cells, and activation-induced cell death.

METHODS:

To study the role of the Fas/FasL pathway in the complex pathophysiology of graft versus host disease (GVHD), we used FasL-deficient B6.gld mice as recipients in a Major Histocompatibility Antigen Complex-matched minor Histocompatibility Antigen-mismatched murine model for GVHD after allogeneic BMT (C3H.SW-->B6).

RESULTS:

We found a significantly higher morbidity and mortality from GVHD compared to control B6 recipients. Histopathological analysis of the GVHD target organs demonstrated that B6.gld recipients developed significantly more thymic and intestinal GVHD. B6gld recipients with GVHD demonstrated an increased expansion of donor T cells and monocytes/ macrophages compared to control B6 recipients, whereas serum TNF-alpha levels were equivalent in B6.gld recipients and control B6 recipients.

CONCLUSION:

This study demonstrates that the expression of FasL in the BMT recipient is important for the host's ability to control GVHD.

• Authors: M R van den Brink, E Moore, K J Horndasch, J M Crawford, G F Murphy, S J Burakoff
• Journal: Transplantation (Transplantation) Vol. 70 Issue 1 Pg. 184-91 (Jul 15 2000) ISSN: 0041-1337 [Print] United States
• PMID: 10919598 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Fas Ligand Protein
• Fasl protein, mouse
• Membrane Glycoproteins
• Tumor Necrosis Factor-alpha

Topics

• Animals
• Bone Marrow Transplantation (adverse effects)
• Disease Susceptibility
• Fas Ligand Protein
• Female
• Graft vs Host Disease (etiology)
• Macrophages (physiology)
• Membrane Glycoproteins (deficiency, physiology)
• Mice
• Mice, Inbred C3H
• Mice, Inbred C57BL
• Monocytes (physiology)
• T-Lymphocytes (immunology)
• Transplantation, Homologous
• Tumor Necrosis Factor-alpha (biosynthesis)