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| Content Provider | PubMed Central |
|---|---|
| Author | Maeda, Masatoshi Ito, Yuji Hatanaka, Takaaki Hashiguchi, Shuhei Torikai, Masaharu Nakashima, Toshihiro Sugimura, Kazuhisa |
| Copyright Year | 2009 |
| Abstract | A costimulatory signal is required for the full activation of T cells, in addition to the antigen-specific signal via the T cell receptor. The inducible costimulator, ICOS is one of the costimulatory molecules that play an essential role in this process, particularly in the expansion or the development of effector T cells. As blocking of the interaction between ICOS and its ligand, B7RP-1, suppresses the T cell response, it can be applied to the treatment of allograft rejection or autoimmune diseases. Here, we isolated four scFv clones that were specific to human B7RP-1 by biopanning a human antibody phage library. We found that three of these clones inhibited the interaction between ICOS-Fc and B7RP-1-Fc. These inhibitory clones not only recognized B7RP-1 molecules expressed on B cells, as assessed by FACS, but also exhibited inhibitory activity in a proliferation assay of T cells stimulated with anti-CD3 mAb and B7RP-1-Fc. Finally, the suppression effect of the scFv on the allogenic immune response was examined using a mixed lymphocyte reaction assay, which demonstrated a successful inhibition of the allogenic reaction, in spite of the high dose needed for complete inhibition (360 nM). |
| Starting Page | 453 |
| File Format | |
| ISSN | 19420870 |
| e-ISSN | 19420870 |
| Journal | mAbs |
| Issue Number | 5 |
| Volume Number | 1 |
| Language | English |
| Publisher | Landes Bioscience |
| Publisher Date | 2009-01-01 |
| Access Restriction | Open |
| Rights Holder | Landes Bioscience |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Immunology and Allergy Immunology |
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