TY - JOUR
T1 - Inhibition of the mixed lymphocyte reaction by T cell vaccination
AU - Lohse, Ansgar W.
AU - Mor, Eitan
AU - Reshef, Tamara
AU - Meyer Zum, Karl‐Hermann ‐H
AU - Büschenfelde,
AU - Cohen, Irun R.
PY - 1990/11
Y1 - 1990/11
N2 - Immunization with attenuated activated autoreactive T cell lines and clones induces a response in syngeneic animals which can induce protection or recovery from autoimmune disease. This process has been termed T cell vaccination. The aim of the present study was to investigate the effect of immunization with MHC‐reactive T cells on the mixed lymphocyte reaction (MLR). By injecting attenuated activated T cells primed for an alloantigen, we markedly reduced the MLR in both rats and mice. This depression appeared to be mediated by active suppression; lymphoid cells from T cell‐vaccinated animals suppressed the MLR responsiveness of T cells from naive animals. Suppression of the MLR was not restricted to the major histocompatibility complex (MHC) alleles used to prime the animals from which the T cell vaccines were prepared; the MLR to other MHC allelic stimulator cells was also suppressed. This MHC‐unrestricted suppression could not be attributed to an anti‐ergotypic response to non‐MHC‐linked activation markers on T cells; an anti‐ergotypic response augmented rather than suppressed the MLR. We herein propose that T cell vaccination might influence the MLR by suppressing the responses of diverse T cells which bear shared T cell receptor idiotypes.
AB - Immunization with attenuated activated autoreactive T cell lines and clones induces a response in syngeneic animals which can induce protection or recovery from autoimmune disease. This process has been termed T cell vaccination. The aim of the present study was to investigate the effect of immunization with MHC‐reactive T cells on the mixed lymphocyte reaction (MLR). By injecting attenuated activated T cells primed for an alloantigen, we markedly reduced the MLR in both rats and mice. This depression appeared to be mediated by active suppression; lymphoid cells from T cell‐vaccinated animals suppressed the MLR responsiveness of T cells from naive animals. Suppression of the MLR was not restricted to the major histocompatibility complex (MHC) alleles used to prime the animals from which the T cell vaccines were prepared; the MLR to other MHC allelic stimulator cells was also suppressed. This MHC‐unrestricted suppression could not be attributed to an anti‐ergotypic response to non‐MHC‐linked activation markers on T cells; an anti‐ergotypic response augmented rather than suppressed the MLR. We herein propose that T cell vaccination might influence the MLR by suppressing the responses of diverse T cells which bear shared T cell receptor idiotypes.
UR - http://www.scopus.com/inward/record.url?scp=0025258509&partnerID=8YFLogxK
U2 - 10.1002/eji.1830201126
DO - 10.1002/eji.1830201126
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C2 - 2147651
AN - SCOPUS:0025258509
SN - 0014-2980
VL - 20
SP - 2521
EP - 2524
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 11
ER -