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- Publisher Website: 10.4049/jimmunol.0900726
- Scopus: eid_2-s2.0-76249085207
- PMID: 20008287
- WOS: WOS:000273447100024
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Article: Nucleotide oligomerization binding domain-like receptor signaling enhances dendritic cell-mediated cross-priming in vivo
Title | Nucleotide oligomerization binding domain-like receptor signaling enhances dendritic cell-mediated cross-priming in vivo |
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Authors | |
Issue Date | 2010 |
Citation | Journal of Immunology, 2010, v. 184, n. 2, p. 736-745 How to Cite? |
Abstract | Nucleotide oligomerization binding domain (Nod)-like receptors are critical cytosolic sensors for the recognition of bacterial peptidoglycan. However, their role in the induction of dendritic cell (DC)-mediated cross-priming remains unclear. In this study, we demonstrate that injecting ligands for Nod1 and Nod2 along with Ag into wild-type mice significantly enhanced the cross-priming of Agspecific CD8+ T cells by CD8α+ DCs, as assessed from the expansion of IFN-γ+ CD8+ T cells, CTL activity against Ag-pulsed targets, and the rejection of transplanted tumors expressing the cognate Ag. The enhancement of CD8α+ DC-mediated cross-priming was likely due to the upregulation of Ag cross-presentation and of costimulatory molecules. Our findings collectively indicate that Nod1/2 signaling is critical for the optimal induction of DC cross-priming in vivo, which may offer an alternative therapeutic pathway in cancer and hosts refractory to TLR signals or paralyzed by viral evasion strategy. Copyright © 2010 by The American Association of Immunologists, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/291940 |
ISSN | 2023 Impact Factor: 3.6 2023 SCImago Journal Rankings: 1.558 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Asano, Jumpei | - |
dc.contributor.author | Tada, Hiroyuki | - |
dc.contributor.author | Onai, Nobuyuki | - |
dc.contributor.author | Sato, Taku | - |
dc.contributor.author | Horie, Yasuo | - |
dc.contributor.author | Fujimoto, Yukari | - |
dc.contributor.author | Fukase, Koichi | - |
dc.contributor.author | Suzuki, Akira | - |
dc.contributor.author | Mak, Tak W. | - |
dc.contributor.author | Ohteki, Toshiaki | - |
dc.date.accessioned | 2020-11-17T14:55:26Z | - |
dc.date.available | 2020-11-17T14:55:26Z | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Journal of Immunology, 2010, v. 184, n. 2, p. 736-745 | - |
dc.identifier.issn | 0022-1767 | - |
dc.identifier.uri | http://hdl.handle.net/10722/291940 | - |
dc.description.abstract | Nucleotide oligomerization binding domain (Nod)-like receptors are critical cytosolic sensors for the recognition of bacterial peptidoglycan. However, their role in the induction of dendritic cell (DC)-mediated cross-priming remains unclear. In this study, we demonstrate that injecting ligands for Nod1 and Nod2 along with Ag into wild-type mice significantly enhanced the cross-priming of Agspecific CD8+ T cells by CD8α+ DCs, as assessed from the expansion of IFN-γ+ CD8+ T cells, CTL activity against Ag-pulsed targets, and the rejection of transplanted tumors expressing the cognate Ag. The enhancement of CD8α+ DC-mediated cross-priming was likely due to the upregulation of Ag cross-presentation and of costimulatory molecules. Our findings collectively indicate that Nod1/2 signaling is critical for the optimal induction of DC cross-priming in vivo, which may offer an alternative therapeutic pathway in cancer and hosts refractory to TLR signals or paralyzed by viral evasion strategy. Copyright © 2010 by The American Association of Immunologists, Inc. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Immunology | - |
dc.title | Nucleotide oligomerization binding domain-like receptor signaling enhances dendritic cell-mediated cross-priming in vivo | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.4049/jimmunol.0900726 | - |
dc.identifier.pmid | 20008287 | - |
dc.identifier.scopus | eid_2-s2.0-76249085207 | - |
dc.identifier.volume | 184 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 736 | - |
dc.identifier.epage | 745 | - |
dc.identifier.eissn | 1550-6606 | - |
dc.identifier.isi | WOS:000273447100024 | - |
dc.identifier.issnl | 0022-1767 | - |