Triple immunosuppression protects murine intracerebral, hippocampal xenografts in adult rat hosts: effects on cellular infiltration, major histocompatibility complex antigen induction and blood-brain barrier leakage

Neuroscience. 1997 Jun;78(3):685-701. doi: 10.1016/s0306-4522(96)00620-3.

Abstract

Recently we reported protection of intracerebral mouse to rat hippocampal xenografts upon treatment with a combination of cyclosporin A, prednisolone and azathioprine. These findings are now supported in an extended analysis of graft-infiltrating cells. Host T-cell and macrophage infiltration and the immunocytochemical level of cellular expression of major histocompatibility complex class I and II antigens, measured by densitometric analysis, were compared between recipient rats receiving cyclosporin A alone or cyclosporin A in combination with prednisolone and azathioprine. The combination therapy resulted in a much improved survival of the xenografted hippocampal tissue with preservation of organotypic granule and pyramidal cell layers. Graft infiltration by T-cells and macrophages was significantly lower and the level of major histocompatibility complex class I and II antigen expression by the infiltrating cells markedly reduced. Lower expression of donor-type major histocompatibility complex class I antigen was also found in the xenografts in the trimedicated recipients, together with reduced blood brain barrier leakage and astrogliosis at the host-graft interface. The results demonstrate the benefits of using combined immunosuppressive strategies for protection of histoincompatible brain xenografts in the central nervous system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier / drug effects
  • Blood-Brain Barrier / physiology*
  • Brain Tissue Transplantation / immunology
  • Brain Tissue Transplantation / physiology*
  • Cell Transplantation / physiology
  • Densitometry
  • Gliosis / pathology
  • Hippocampus / cytology
  • Hippocampus / transplantation*
  • Immunoglobulin G / metabolism
  • Immunohistochemistry
  • Immunosuppressive Agents / pharmacology*
  • Leukocyte Common Antigens / biosynthesis
  • Leukocytes / immunology
  • Major Histocompatibility Complex / immunology
  • Major Histocompatibility Complex / physiology*
  • Male
  • Mice
  • Oligodendroglia / drug effects
  • Rats
  • Rats, Wistar
  • Transplantation, Heterologous / immunology
  • Transplantation, Heterologous / physiology*

Substances

  • Immunoglobulin G
  • Immunosuppressive Agents
  • Leukocyte Common Antigens