Harnessing MerTK agonism for targeted therapeutics

Phagocytosis plays important roles both in homeostasis and under pathological conditions. Fcγ receptor-mediated phagocytosis has been exploited as an integral mechanism for antibody-based therapies. Unlike Fcγ receptor-mediated phagocytosis, MerTK-mediated phagocytic clearance is immunologically sil...

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Bibliographic Details
Main Authors: Vivekananda Kedage (Author), Diego Ellerman (Author), Yongmei Chen (Author), Wei-Ching Liang (Author), Joven Borneo (Author), Yan Wu (Author), Minhong Yan (Author)
Format: Book
Published: Taylor & Francis Group, 2020-01-01T00:00:00Z.
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Summary:Phagocytosis plays important roles both in homeostasis and under pathological conditions. Fcγ receptor-mediated phagocytosis has been exploited as an integral mechanism for antibody-based therapies. Unlike Fcγ receptor-mediated phagocytosis, MerTK-mediated phagocytic clearance is immunologically silent. Here, we describe a bispecific antibody approach to harness MerTK for targeted clearance without inducing proinflammatory cytokine release associated with Fcγ receptor engagement. We generated bispecific antibodies targeting live B cells or amyloid beta aggregates to demonstrate the feasibility and versatility of this new approach.
Item Description:10.1080/19420862.2019.1685832
1942-0870
1942-0862