MODULATION OF THE IMMUNE RESPONSE
    41.
    发明申请
    MODULATION OF THE IMMUNE RESPONSE 审中-公开
    调节免疫应答

    公开(公告)号:US20150225457A1

    公开(公告)日:2015-08-13

    申请号:US14418726

    申请日:2013-07-30

    摘要: Described herein are compositions and methods for the modulation of T-cell tolerance, which can be upregulated or down regulated by concurrent enhancement or inhibition of CEACAM1/TIM3 interactions. As described herein, the discovery that CEACAM1 is a direct ligand of TIM3 and vice versa has been shown in cis and in trans. In addition, as demonstrated herein, CEACAM1 and TIM3 are co-regulated during the course of T-cell activation.

    摘要翻译: 本文描述了用于调节T细胞耐受性的组合物和方法,其可以通过同时增强或抑制CEACAM1 / TIM3相互作用而被上调或下调。 如本文所述,CEACAM1是TIM3的直接配体,反之亦然的发现已经以顺式和反式表示。 此外,如本文所示,CEACAM1和TIM3在T细胞活化过程中共调节。

    REGULATORS OF B CELL-MEDIATED IMMUNOSUPPRESSION

    公开(公告)号:US20190225701A1

    公开(公告)日:2019-07-25

    申请号:US16336635

    申请日:2017-09-26

    摘要: The compositions and methods described herein are based, in part, on the discovery that regulatory B cells (Bregs) differentially express a specific set of coinhibitory molecules, including TIGIT, LAG-3, PD-1, CTLA4, and TIM-3. The data described herein indicate that TIGIT is required for both Breg-mediated tolerance maintenance at the steady state, and inflammation restraint during autoimmune and inflammatory diseases. Accordingly, provided herein are compositions and methods targeting coinhibitory molecules, such as TIGIT, LAG-3, PD-1, CTLA4, and TIM-3, in B cells, as novel therapeutic strategies for modulating immune suppression and treating diseases mediated or impacted by immune suppression mechanisms, such as autoimmune diseases and cancers.