Anatomically Restricted Synergistic Antiviral Activities of Innate and Adaptive Immune Cells in the Skin

Autor: Jonathan W. Yewdell, Barbara Molon, Javier G. Magadán, Jack R. Bennink, Barbara F. Ngudiankama, Stephanie S. Cush, Glennys V. Reynoso, Heather D. Hickman, Vincenzo Bronte, James S. Gibbs, Erica J. Rubin
Jazyk: angličtina
Předmět:
Keratinocytes
Chemokine
Cancer Research
Immunology and Microbiology (all)
Cell
Adaptive Immunity
CD8-Positive T-Lymphocytes
Monocytes
Mice
Cell Movement
Vaccinia
Innate
Antigens
Ly

Viral
Microscopy
biology
reactive nitrogen species
Antigens

Ly
Chemokines
Ly6G antigen

mouse
Peroxynitrous Acid

Viral Load
Acquired immune system
Reactive Nitrogen Species
medicine.anatomical_structure
Administration
Skin Diseases
Viral

medicine.symptom
Chemokines
Inflammation
Vaccinia virus
Administration
Cutaneous

Microbiology
Animals
Epidermis
Microscopy
Fluorescence
Multiphoton

Peroxynitrous Acid
Immunity
Innate

Molecular Biology
Skin Diseases
Virus
Article
Fluorescence
Immune system
Immunology and Microbiology(all)
Virology
medicine
Antigens
Ly6G antigen
mouse
Multiphoton
Innate immune system
Immunity
Cutaneous
Ly
Immunology
biology.protein
Parasitology
CD8
Zdroj: Cell Host & Microbe. (2):155-168
ISSN: 1931-3128
DOI: 10.1016/j.chom.2013.01.004
Popis: Summary Despite extensive ex vivo investigation, the spatiotemporal organization of immune cells interacting with virus-infected cells in tissues remains uncertain. To address this, we used intravital multiphoton microscopy to visualize immune cell interactions with virus-infected cells following epicutaneous vaccinia virus (VV) infection of mice. VV infects keratinocytes in epidermal foci and numerous migratory dermal inflammatory monocytes that outlie the foci. We observed Ly6G + innate immune cells infiltrating and controlling foci, while CD8 + T cells remained on the periphery killing infected monocytes. Most antigen-specific CD8 + T cells in the skin did not interact with virus-infected cells. Blocking the generation of reactive nitrogen species relocated CD8 + T cells into foci, modestly reducing viral titers. Depletion of Ly6G + and CD8 + cells dramatically increased viral titers, consistent with their synergistic but spatially segregated viral clearance activities. These findings highlight previously unappreciated differences in the anatomic specialization of antiviral immune cell subsets.
Databáze: OpenAIRE