Prevention of graft-versus-host disease by peptides binding to class II major histocompatibility complex molecules.

Journal Article (Journal Article)

Graft-versus-host disease across minor histocompatibility barriers was induced in two different models by transplanting allogeneic bone marrow and spleen cells into irradiated H-2-compatible recipient mice. In this report, we show that administration of peptides with high binding affinity for the respective class II major histocompatibility complex molecules after transplantation is capable of preventing the development of graft-versus-host disease in two different murine models. The peptides used were myelin basic protein residues 1 through 11 with alanine at position 4 (Ac 1-11[4A]) for I-Au (A alpha uA beta u), and the antigenic core sequence 323 through 339 of ovalbumin with lysine and methionine extension (KM core) for I-As (A alpha sA beta s). In both systems, the mechanism of prevention was found to be major histocompatibility complex-associated, because nonbinding control peptides did not have any effect. Engraftment of allogeneic bone marrow cells was shown by polymerase chain reaction analysis of DNA polymorphisms in a microsatellite region within the murine interleukin-5 gene.

Full Text

Duke Authors

Cited Authors

  • Schlegel, PG; Aharoni, R; Smilek, DE; Fernandez, LP; McDevitt, HO; Tran, N; Vaysburd, M; Chao, NJ

Published Date

  • October 15, 1994

Published In

Volume / Issue

  • 84 / 8

Start / End Page

  • 2802 - 2810

PubMed ID

  • 7522644

International Standard Serial Number (ISSN)

  • 0006-4971


  • eng

Conference Location

  • United States