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Allogeneic IgG combined with dendritic cell stimuli induce antitumour T-cell immunity

Yaron Carmi (), Matthew H. Spitzer, Ian L. Linde, Bryan M. Burt, Tyler R. Prestwood, Nicola Perlman, Matthew G. Davidson, Justin A. Kenkel, Ehud Segal, Ganesh V. Pusapati, Nupur Bhattacharya and Edgar G. Engleman ()
Additional contact information
Yaron Carmi: School of Medicine, Stanford University
Matthew H. Spitzer: School of Medicine, Stanford University
Ian L. Linde: School of Medicine, Stanford University
Bryan M. Burt: School of Medicine, Stanford University
Tyler R. Prestwood: School of Medicine, Stanford University
Nicola Perlman: School of Medicine, Stanford University
Matthew G. Davidson: School of Medicine, Stanford University
Justin A. Kenkel: School of Medicine, Stanford University
Ehud Segal: School of Medicine, Stanford University
Ganesh V. Pusapati: School of Medicine, Stanford University
Nupur Bhattacharya: School of Medicine, Stanford University
Edgar G. Engleman: School of Medicine, Stanford University

Nature, 2015, vol. 521, issue 7550, 99-104

Abstract: Naturally occurring tumour-binding IgG antibodies are shown to initiate the rejection of allogeneic tumours, whereby Fc-receptor-mediated uptake of tumour immune complexes into dendritic cells activates tumour-reactive T cells, and intra-tumoral injection of allogeneic IgG together with dendritic cell adjuvants induces systemic T-cell-mediated antitumour responses.

Date: 2015
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DOI: 10.1038/nature14424

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