CD28/B7 MEDIATED COSTIMULATION IS REQUIRED FOR PARATHYROID GLAND ALLOGRAFT REJECTION IN RATS
Chinese Medical Sciences JournalIssue 3, (1999)
Updated:2024-04-10
Share with wechat friends or circle of friends
Export references
CD28/B7 MEDIATED COSTIMULATION IS REQUIRED FOR PARATHYROID GLAND ALLOGRAFT REJECTION IN RATS
Affiliations:
Author bio:
Funds:
DOI:
CLC:R653
Published:1999
Accepted:
Scan QR Code
[1]肖毅,朱预,陈力真,王树蕙,何小东.CD28/B7-MEDIATED COSTIMULATION IS REQUIRED FOR PARATHYROID GLAND ALLOGRAFT REJECTION IN RATS[J].Chinese Medical Sciences Journal,1999(03):33-37.
Xiao Yi △. CD28/B7 MEDIATED COSTIMULATION IS REQUIRED FOR PARATHYROID GLAND ALLOGRAFT REJECTION IN RATS[J]. Chinese medical sciences journal, 1999, (3).
[1]肖毅,朱预,陈力真,王树蕙,何小东.CD28/B7-MEDIATED COSTIMULATION IS REQUIRED FOR PARATHYROID GLAND ALLOGRAFT REJECTION IN RATS[J].Chinese Medical Sciences Journal,1999(03):33-37.DOI:
Xiao Yi △. CD28/B7 MEDIATED COSTIMULATION IS REQUIRED FOR PARATHYROID GLAND ALLOGRAFT REJECTION IN RATS[J]. Chinese medical sciences journal, 1999, (3).DOI:
CD28/B7 MEDIATED COSTIMULATION IS REQUIRED FOR PARATHYROID GLAND ALLOGRAFT REJECTION IN RATS
The activation of T cells to differentiate and to proliferate is an essential step in the immune response to antigen
especially in cell mediated acute allograft rejection. Besides the interaction of CD3/TCR complex with Ag/MHC complex presented on antigen presenting cells
a complete T cell activation and proliferation requires a second costimulatory signal. The interaction of CD28/CTLA 4 and B7 is a major costimulatory pathway for T Cell activation. Inhibition of this pathway results in development of antigen specific unresponsiveness and clonal anergy.In present study
the biologic function of anti CD28 monoclonal antibody and its Fab fragment were investigated in vitro and in vivo.The results indicate that mAbCD28 and its Fab fragments could promote the functional recovery of allografts and prolong the graft survival
but could not reverse the acute rejection or induce transplantation tolerance in the rat PTG allograft model. We also found that peripheral TNF α level and NK cell activity were suppressed in the presence of mAbCD28 and its Fab fragments for a relatively long time after PTG transplantation.