Non-standard viral genome-derived RNA activates TLR3 and type I IFN signaling to induce cDC1-dependent CD8+ T-cell responses during vaccination in mice

•DDO generates a local type I IFN and inflammatory response.•DDO induces accumulation of cDC1s in the draining lymph node.•Response is not identical to Poly:IC, a known TLR3 sensor and Type I IFN stimulator.•Type I IFN signaling and TLR3 mediate DDO induced cDC1 accumulation.•Loss of cDC1s in draini...

Full description

Saved in:
Bibliographic Details
Published inVaccine Vol. 40; no. 50; pp. 7270 - 7279
Main Authors Fisher, Devin G., Gnazzo, Victoria, Holthausen, David J., López, Carolina B.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 28.11.2022
Elsevier Limited
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•DDO generates a local type I IFN and inflammatory response.•DDO induces accumulation of cDC1s in the draining lymph node.•Response is not identical to Poly:IC, a known TLR3 sensor and Type I IFN stimulator.•Type I IFN signaling and TLR3 mediate DDO induced cDC1 accumulation.•Loss of cDC1s in draining LNs stops development of antigen specific CD8 + T cells. There is a critical need to develop vaccine adjuvants that induce robust immune responses able to protect against intracellular pathogens, including viruses. Previously, we described defective viral genome-derived oligonucleotides (DDOs) as novel adjuvants that strongly induce type 1 immune responses, including protective Th1 CD4+ T-cells and effector CD8+ T-cells in mice. Here, we unravel the early innate response required for this type 1 immunity induction. Upon DDO subcutaneous injection, type 1 conventional dendritic cells (cDC1s) accumulate rapidly in the draining lymph node in a Toll-like receptor 3 (TLR3)- and type I interferon (IFN)-dependent manner. cDC1 accumulation in the lymph node is required for antigen-specific CD8+ T-cell responses. Notably, in contrast to poly I:C, DDO administration resulted in type I IFN expression at the injection site, but not in the draining lymph node. Additionally, DDOs induced an inflammatory cytokine profile distinct from that induced by poly I:C. Therefore, DDOs represent a powerful new adjuvant to be used during vaccination against intracellular pathogens.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0264-410X
1873-2518
DOI:10.1016/j.vaccine.2022.10.052