To analyze in vivo the induction of B cell tolerance against a T cell surface antigen, we generated transgenic mice expressing an anti-CD8.2 mu heavy chain gene. We show that self-specific B cells are efficiently tolerized if they express the membrane-bound form of the transgenic mu chain on their surface but that they can escape tolerization if they express only the secreted form. In the latter, we find an enhanced expression of anti-CD8.2 antibodies after polyclonal B cell activation. As a result, transgenic anti-CD8.2 antibodies bind to the CD8+ T cells but they did not induce their elimination. Furthermore, we observed the preferential expression of a limited subset of endogenous light chains with the transgenic mu chain. This suggests a positive or negative selection for particular heavy and light chain combinations in B lymphocytes.
Skip Nav Destination
Article navigation
1 December 1991
Article|
December 01 1991
B cell tolerance in mice transgenic for anti-CD8 immunoglobulin mu chain.
F Brombacher,
F Brombacher
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Search for other works by this author on:
G Köhler,
G Köhler
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Search for other works by this author on:
H Eibel
H Eibel
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Search for other works by this author on:
F Brombacher
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
G Köhler
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
H Eibel
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1991) 174 (6): 1335–1346.
Citation
F Brombacher, G Köhler, H Eibel; B cell tolerance in mice transgenic for anti-CD8 immunoglobulin mu chain.. J Exp Med 1 December 1991; 174 (6): 1335–1346. doi: https://doi.org/10.1084/jem.174.6.1335
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 InstitutionEmail alerts
Advertisement