About this item:

1,473 Views | 169 Downloads

Author Notes:

Correspondence: Rama Rao Amara, Phone: (404) 727-8765; FAX: (404) 727-7768; ramara@emory.edu

Acknowledgments We are grateful to Dr. Shizuo Akira for kindly providing us with Zbp1−/− mice.

We thank the veterinary staff at the Yerkes Division of Research Resources for their support and H. Drake-Perrow for administrative support.

We also thank the Emory CFAR virology core for qPCR measurements.

Subjects:

Research Funding:

This work was supported by the National Institutes of Health/National Institute of Allergy and Infectious Diseases grants R01 AI057029 and R01 AI071852 to RRA; Yerkes National Primate Research Center base grant, P51 RR00165; Emory CFAR grant P30 AI050409.

Adenovirus Type 5 Induces Vitamin A–Metabolizing Enzymes in Dendritic Cells and Enhances Priming of Gut Homing CD8 T Cells

Tools:

Journal Title:

Mucosal Immunology

Volume:

Volume 4, Number 5

Publisher:

, Pages 528-538

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Protective immunity at the gut-associated mucosal tissue is induced primarily by oral/rectal immunization owing to the need for targeting antigen to the gut-resident dendritic cells (DC). Here we show that an adenovirus type 5 (Ad5) based HIV-1 vaccine can prime a durable antigen-specific CD8 T cell response in the gut following intramuscular immunization in mice. The ability of Ad5 to prime gut homing CD8 T cells in vivo was associated with Ad5-induced expression of retinal dehydrogenase (RALDH) enzymes in conventional DC. The Ad5-mediated induction of RALDH did not require signaling through toll-like receptors, DNA-dependent activator of IRFs and several MAP kinases, or replication capacity of the virus, but was dependant on NF-κB and granulocyte-macrophage colony-stimulating factor. These results provide an innate mechanism through which Ad5-stimulated DC prime gut homing CD8 T cells and have implications for the development of novel mucosal adjuvants for subunit vaccines administered via the intramuscular route.

Copyright information:

© 2011, Rights Managed by Nature Publishing Group

Export to EndNote