Tolerance, as defined by an inability to produce runt disease and the failure to elicit a normal lymphocyte transfer reaction, was induced in Lewis and Brown Norway rats by the neonatal injection of bone marrow from the opposite strain. When thymus, thoracic duct lymph, or lymph node cells from such tolerant Lewis and Brown Norway rats were cultured together, or were individually cultured with similar cells from an F1 hybrid of these strains, transformation was suppressed to the levels observed in nonmixed control cultures. In contrast, mixtures of cells involving nontolerant donors demonstrated significant transformation as measured by per cent enlarged cells and thymidine-3H uptake. The specificity of the tolerance was confirmed by the presence of transformed cells in mixtures involving cells from a tolerant donor and an unrelated or a partially related third strain of rats. From these results, it is suggested that the mixed lymphocyte reaction may be used as a simple test for tolerance and that it most likely represents an in vitro immune response.
Skip Nav Destination
Article navigation
1 May 1968
Article|
May 01 1968
THE MIXED LYMPHOCYTE REACTION: AN IN VITRO TEST FOR TOLERANCE
M. Roy Schwarz
M. Roy Schwarz
From the Department of Biological Structure, the University of Washington, Seattle, Washington 98105
Search for other works by this author on:
M. Roy Schwarz
From the Department of Biological Structure, the University of Washington, Seattle, Washington 98105
Received:
December 17 1967
Online ISSN: 1540-9538
Print ISSN: 0022-1007
Copyright © 1968 by The Rockefeller University Press
1968
J Exp Med (1968) 127 (5): 879–890.
Article history
Received:
December 17 1967
Citation
M. Roy Schwarz; THE MIXED LYMPHOCYTE REACTION: AN IN VITRO TEST FOR TOLERANCE . J Exp Med 1 May 1968; 127 (5): 879–890. doi: https://doi.org/10.1084/jem.127.5.879
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement