Journal article
Influenza-infected neutrophils within the infected lungs act as antigen presenting cells for anti-viral CD8(+) T cells
PloS one, Vol.7(10), pp.e46581-e46581
2012
DOI: 10.1371/journal.pone.0046581
PMCID: PMC3466305
PMID: 23056353
Abstract
Influenza A virus (IAV) is a leading cause of respiratory tract disease worldwide. Anti-viral CD8(+) T lymphocytes responding to IAV infection are believed to eliminate virally infected cells by direct cytolysis but may also contribute to pulmonary inflammation and tissue damage via the release of pro-inflammatory mediators following recognition of viral antigen displaying cells. We have previously demonstrated that IAV antigen expressing inflammatory cells of hematopoietic origin within the infected lung interstitium serve as antigen presenting cells (APC) for infiltrating effector CD8(+) T lymphocytes; however, the spectrum of inflammatory cell types capable of serving as APC was not determined. Here, we demonstrate that viral antigen displaying neutrophils infiltrating the IAV infected lungs are an important cell type capable of acting as APC for effector CD8(+) T lymphocytes in the infected lungs and that neutrophils expressing viral antigen as a result of direct infection by IAV exhibit the most potent APC activity. Our findings suggest that in addition to their suggested role in induction of the innate immune responses to IAV, virus clearance, and the development of pulmonary injury, neutrophils can serve as APCs to anti-viral effector CD8(+) T cells within the infected lung interstitium.
Details
- Title: Subtitle
- Influenza-infected neutrophils within the infected lungs act as antigen presenting cells for anti-viral CD8(+) T cells
- Creators
- Matthew M Hufford - Beirne B. Carter Center for Immunology Research, The University of Virginia, Charlottesville, Virginia, USAGraham RichardsonHaixia ZhouBalaji Manicassamy - University of Iowa, Microbiology and ImmunologyAdolfo García-Sastre - Icahn School of Medicine at Mount SinaiRichard I EnelowThomas J Braciale
- Resource Type
- Journal article
- Publication Details
- PloS one, Vol.7(10), pp.e46581-e46581
- DOI
- 10.1371/journal.pone.0046581
- PMID
- 23056353
- PMCID
- PMC3466305
- NLM abbreviation
- PLoS One
- ISSN
- 1932-6203
- eISSN
- 1932-6203
- Grant note
- U-10 AI-83024 / NIAID NIH HHS T32 AI007496-13 / NIAID NIH HHS R01 AI-37293 / NIAID NIH HHS R01 AI037293 / NIAID NIH HHS K99 AI095320 / NIAID NIH HHS R01 AI-15608 / NIAID NIH HHS U01 AI095611 / NIAID NIH HHS R01 HL-33391 / NHLBI NIH HHS R01 AI015608 / NIAID NIH HHS U01 AI-095611 / NIAID NIH HHS R01 HL033391 / NHLBI NIH HHS 1K99 AI095320-01 / NIAID NIH HHS U19 AI-083025 / NIAID NIH HHS U19 AI083025 / NIAID NIH HHS U-19 AI-83024 / NIAID NIH HHS U19 AI083024 / NIAID NIH HHS T32 AI055432 / NIAID NIH HHS T32 AI007496 / NIAID NIH HHS
- Language
- English
- Date published
- 2012
- Academic Unit
- Microbiology and Immunology
- Record Identifier
- 9984210057302771
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