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Tumor-binding antibodies induce potent dendritic cell-mediated tumor immunity

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Article: e1078063 | Received 24 Jul 2015, Accepted 24 Jul 2015, Published online: 07 May 2018

Figures & data

Figure 1. Proposed mechanism to explain how antitumor alloantibodies initiate T cell immunity. In the typical tumor microenvironment, which is highly immunosuppressive, tumor-associated DC cannot transmit a signal through their Fcγ receptors following engagement of IgG bound to tumor antigens/cells. Administration of tumor-binding IgG in combination with TNFα and CD40L enables tumor DC to internalize tumor antigens through Fcγ receptors, which transmit a danger signal. These antigens are then processed by the DC and subsequently presented to T cells, which attack both the primary tumor as well as distant metastases.

Figure 1. Proposed mechanism to explain how antitumor alloantibodies initiate T cell immunity. In the typical tumor microenvironment, which is highly immunosuppressive, tumor-associated DC cannot transmit a signal through their Fcγ receptors following engagement of IgG bound to tumor antigens/cells. Administration of tumor-binding IgG in combination with TNFα and CD40L enables tumor DC to internalize tumor antigens through Fcγ receptors, which transmit a danger signal. These antigens are then processed by the DC and subsequently presented to T cells, which attack both the primary tumor as well as distant metastases.

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