Innate immunity defines the capacity of antiviral T cells to limit persistent infection

Author:

Andrews Daniel M.12,Estcourt Marie J.12,Andoniou Christopher E.12,Wikstrom Matthew E.12,Khong Andrea12,Voigt Valentina12,Fleming Peter12,Tabarias Hyacinth12,Hill Geoffrey R.3,van der Most Robbert G.1,Scalzo Anthony A.12,Smyth Mark J.4,Degli-Esposti Mariapia A.12

Affiliation:

1. Immunology and Virology Program, Centre for Ophthalmology and Visual Science, University Department of Medicine, University of Western Australia, Nedlands, Western Australia 6009, Australia

2. Centre for Experimental Immunology, Lions Eye Institute, Nedlands, Western Australia 6009, Australia

3. Bone Marrow Transplantation Laboratory, Queensland Institute of Medical Research, Herston, Queensland 4006, Australia

4. Cancer Immunology Program, Sir Donald and Lady Trescowthick Laboratories, Peter MacCallum Cancer Centre, East Melbourne, Victoria 3002, Australia

Abstract

Effective immunity requires the coordinated activation of innate and adaptive immune responses. Natural killer (NK) cells are central innate immune effectors, but can also affect the generation of acquired immune responses to viruses and malignancies. How NK cells influence the efficacy of adaptive immunity, however, is poorly understood. Here, we show that NK cells negatively regulate the duration and effectiveness of virus-specific CD4+ and CD8+ T cell responses by limiting exposure of T cells to infected antigen-presenting cells. This impacts the quality of T cell responses and the ability to limit viral persistence. Our studies provide unexpected insights into novel interplays between innate and adaptive immune effectors, and define the critical requirements for efficient control of viral persistence.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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