Evidence that anti-LFA-1 in vivo improves engraftment and survival after allogeneic bone marrow transplantation

Transplantation. 1990 May;49(5):882-6. doi: 10.1097/00007890-199005000-00009.

Abstract

The LFA-1 molecule is a member of the leukocyte adhesion complex (CD11/CD18) that is critical to adhesion and effector function of T cells and NK cells. Both T cells and NK cells play important roles in bone marrow graft rejection, and anti-LFA-1 MAbs inhibit in vitro T cell and NK cell cytotoxicity. We here describe the in vivo use of a monoclonal antibody to the alpha chain of LFA-1 (CD11a) to prevent rejection of T cell-depleted allogeneic bone marrow. Animals receiving anti-LFA-1 and 1100 cGy total-body irradiation showed improved hemopoietic and immunologic reconstitution one month after BMT when compared with animals receiving TBI alone. Animals in the anti-LFA-1 group showed significantly improved long-term survival, and had no deficits in long-term lymphohemopoietic reconstitution.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / therapeutic use*
  • Antigens, Differentiation / immunology*
  • Bone Marrow Transplantation / immunology*
  • Cell Separation
  • Graft Survival*
  • Hematopoiesis
  • Immunity
  • Lymphocyte Function-Associated Antigen-1
  • Mice
  • Mice, Inbred Strains
  • Receptors, Leukocyte-Adhesion / immunology*
  • T-Lymphocytes / immunology
  • Time Factors

Substances

  • Antibodies, Monoclonal
  • Antigens, Differentiation
  • Lymphocyte Function-Associated Antigen-1
  • Receptors, Leukocyte-Adhesion