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Published on: February 10, 2022
Persistent antigen presentation after acute vesicular stomatitis virus infection
Damian L Turner1, Linda S Cauley, Kamal M Khanna
1Department of Immunology, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030-1319, USA.
Protracted antigen presentation after vesicular stomatitis virus (VSV) infection, even when acute, may prolong T-cell responses. This suggests a novel mechanism for sustained antiviral immunity.
Area of Science:
- Immunology
- Virology
- Cellular Biology
Background:
- Long-term antigen expression is crucial for modulating T-cell responses in chronic viral infections.
- Emerging evidence indicates immune responses can manifest late after seemingly acute viral infections.
Purpose of the Study:
- To investigate the CD8 T-cell response to vesicular stomatitis virus (VSV), an infection typically associated with rapid viral clearance.
- To determine the duration and location of antigen presentation following VSV infection.
Main Methods:
- Analysis of CD8 T-cell responses to intranasal VSV infection in mice.
- Detection of virus-encoded antigen in lymph nodes using adoptively transferred CD8 T cells.
- Comparison of antigen presentation duration between VSV and Listeria monocytogenes infections.
- Observation of T-cell clustering and dendritic cell interactions within lymph nodes.
- Phenotypic and functional characterization of late-emerging memory CD8 T cells.
Main Results:
- Virus-encoded antigen remained detectable for over 6 weeks post-infection in both draining and nondraining lymph nodes.
- Prolonged antigen presentation was specific to VSV infection, not observed with Listeria monocytogenes.
- Late after VSV infection, antigen-specific CD8 T cells formed clusters with dendritic cells in lymph nodes.
- Naïve CD8 T cells generated memory cells exhibiting characteristic phenotypes and functions.
Conclusions:
- Protracted antigen presentation occurs after apparently acute VSV infections.
- This sustained antigen presentation may contribute to ongoing antiviral immune responses.
- The findings challenge the notion of rapid clearance limiting T-cell engagement in acute viral infections.
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