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Fc-γ receptor-mediated crosslinking co-defines the immunostimulatory activity of anti-human CD96 antibodies.

Rogel, A., Ibrahim, F. M., Thirdborough, S. M., Renart-Depontieu, F., Birts, C. N., Buchan, S. L., Preville, X., King, E. V. and Al-Shamkhani, A., 2022. Fc-γ receptor-mediated crosslinking co-defines the immunostimulatory activity of anti-human CD96 antibodies. JCI Insight, 7 (19), e158444.

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158444.2-20220926101445-covered-e0fd13ba177f913fd3156f593ead4cfd.pdf - Published Version
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Final CD96 paper.pdf - Published Version
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DOI: 10.1172/jci.insight.158444


New strategies that augment T-cell responses are required to broaden the therapeutic arsenal against cancer. CD96, TIGIT and CD226 are receptors that bind to a communal ligand, CD155, and transduce either inhibitory or activating signals. Whereas the function of TIGIT and CD226 is established, the role of CD96 remains ambiguous. Using a panel of engineered antibodies, we discovered that the T-cell stimulatory activity of anti-CD96 antibodies requires antibody crosslinking and is potentiated by Fc-gamma receptors. Thus, soluble 'Fc silent' anti-CD96 antibodies failed to stimulate human T cells, whereas the same antibodies were stimulatory after coating onto plastic surfaces. Remarkably, the activity of soluble anti-CD96 antibodies was reinstated by engineering the Fc domain to a human IgG1 isotype and was dependent on antibody trans-crosslinking by Fc-γRI. In contrast, neither human IgG2 nor variants with increased Fc-γ receptor IIB binding possessed stimulatory activity. Anti-CD96 antibodies acted directly on T cells and augmented gene expression networks associated with T-cell activation, leading to proliferation, cytokine secretion and resistance to regulatory T-cell suppression. Furthermore, CD96 expression correlated with survival in HPV+ head and neck squamous cell carcinoma and its crosslinking activated tumor-infiltrating T cells, thus highlighting the potential of anti-CD96 antibodies in cancer immunotherapy. .

Item Type:Article
Uncontrolled Keywords:Cancer immunotherapy; Costimulation; Immunology; T cells
Group:Faculty of Science & Technology
ID Code:37427
Deposited By: Symplectic RT2
Deposited On:05 Sep 2022 10:05
Last Modified:24 Jan 2023 10:01


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