WDFY4 is required for cross-presentation in response to viral and tumor antigens

Author:

Theisen Derek J.1ORCID,Davidson Jesse T.12ORCID,Briseño Carlos G.1,Gargaro Marco3ORCID,Lauron Elvin J.4ORCID,Wang Qiuling5,Desai Pritesh15ORCID,Durai Vivek1,Bagadia Prachi1,Brickner Joshua R.1ORCID,Beatty Wandy L.5ORCID,Virgin Herbert W.16ORCID,Gillanders William E.27,Mosammaparast Nima1,Diamond Michael S.1589ORCID,Sibley L. David5ORCID,Yokoyama Wayne4ORCID,Schreiber Robert D.19ORCID,Murphy Theresa L.1ORCID,Murphy Kenneth M.110ORCID

Affiliation:

1. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.

2. Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.

3. Department of Experimental Medicine, University of Perugia, Perugia, Italy.

4. Division of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

5. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.

6. Vir Biotechnology, San Francisco, CA, USA.

7. Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine, St. Louis, MO 63110, USA.

8. Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

9. Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO 63110, USA.

10. Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, MO 63110, USA.

Abstract

Adding to the cross-presentation family Immune responses to viral or tumor antigens are typically initiated by the process of cross-presentation. Cross-presentation is believed to be the major way that innate immune cells, such as the classical dendritic cell 1 (cDC1) subset, activate and prime immunological T cells. Theisen et al. used CRISPR-based screening to identify regulators of cross-presentation by cDC1s (see the Perspective by Barbet and Blander). One such regulator that was identified, WDFY4 (WD repeat- and FYVE domain–containing protein 4), was required for cross-presentation of cell- and bacterial-associated antigens. WDFY4 played a critical role in cDC1-mediated viral and tumor immunity yet did not seem necessary for major histocompatibility complex class II presentation or for cross-presentation by monocyte-derived DCs. Science , this issue p. 694 ; see also p. 641

Funder

Howard Hughes Medical Institute

National Cancer Institute

National Institute of Allergy and Infectious Diseases

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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