What is it about?
The killing of regulatory T cells (Tregs) that infiltrate cancer may represent a way to favor tumor rejection by the immune system of the host. Antibodies against proteins expressed mainly on the surface of Tregs (Treg markers) can promote the killing of Tregs by a mechanism called antibody-dependent cell-mediated cytotoxicity (ADCC). We investigated the mRNA expression of 24 Treg markers in 5728 human cancer samples to discover which is/are the best Treg marker(s) that can be targeted by antibodies to cause ADCC.
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Why is it important?
Our study suggests that the ADCC strategy is unlikely to promote tumor rejection in 5 cancers (colorectal, liver, prostate and two kinds of ovarian cancers) but can succeed in 4 cancers (breast, renal and two kinds of lung cancers). Antibodies against 4-1BB, CD39, galectin-9, GITR, IL-21R, LAP, neuropilin-1, TIGIT, and TNFR2 are likely to promote ADCC in these cancers. However, not all antibodies are forecasted to work to the same extent in all tumors. For example, anti-LAP appears to be the best in the treatment of renal cell carcinoma, anti-GITR in the treatment of squamous NSCLC and anti-TIGIT in the treatment of non-squamous NSCLC.
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This page is a summary of: Potential effect of tumor-specific Treg-targeted antibodies in the treatment of human cancers: A bioinformatics analysis, OncoImmunology, November 2017, Taylor & Francis,
DOI: 10.1080/2162402x.2017.1387705.
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