Target Validation Information | |||||
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Target ID | T15000 | ||||
Target Name | Cytotoxic T-lymphocyte protein 4 | ||||
Target Type | Successful |
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Drug Potency against Target | Tremelimumab | Drug Info | IC50 = 0.5~0.65 nM | ||
Action against Disease Model | Tremelimumab | Tremelim uMab (anti-CTLA4) mediates immune responses mainly by direct activation of T effector cells rather than by affecting T regulatory cells. Tremelim uMab enhanced the proliferative response of T effector cells (Teff) upon TCR stimulation, and abrogated Treg suppressive ability. In the presence of tremelim uMab, frequencies of IL-2-secreting CD4(+) T cells and IFN-|??secreting CD4(+) and CD8(+) T cells were increased in response to polyclonal activation and t uMor antigens. | [553079] | Drug Info | |
The Effect of Target Knockout, Knockdown or Genetic Variations | The critical homeostasis mediated by CTLA-4 was proven using monoclonal antibodies and genetically disrupted CTLA-4 knockout mice that develop polyclonal lymphocyte activation and proliferation leading to massively enlarged lymph nodes and spleen and fatal multiorgan lymphocytic infiltrates. CTLA-4 ligation following T-cell activation downregulates cytokine production and cell-cycle progression, however, the proximal biochemical basis for robust T-cell regulation remains unclear. In this review, we s uMmarize studies supporting a dynamic role for CTLA-4 at the immunological synapse leading to direct attenuation of early cell signals. A model is proposed based on these observations, which proposes that CTLA-4 may, in fact, function under some circ uMstances in a ligand-independent manner. | [553079] | |||
References | |||||
Ref 553079 | Tremelimumab (anti-CTLA4) mediates immune responses mainly by direct activation of T effector cells rather than by affecting T regulatory cells. Clin Immunol. 2011 Jan;138(1):85-96. doi: 10.1016/j.clim.2010.09.011. Epub 2010 Nov 5. |
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