Dendritic cells are responsible for the capacity of CpG oligodeoxynucleotides to act as an adjuvant for protective vaccine immunity against Leishmania major in mice
about
Coadministration of polyinosinic:polycytidylic acid and immunostimulatory complexes modifies antigen processing in dendritic cell subsets and enhances HIV gag-specific T cell immunity.HIV Gag protein conjugated to a Toll-like receptor 7/8 agonist improves the magnitude and quality of Th1 and CD8+ T cell responses in nonhuman primates.Alum adjuvant boosts adaptive immunity by inducing uric acid and activating inflammatory dendritic cells.Coinjection with TLR2 agonist Pam3CSK4 reduces the pathology of leishmanization in mice.Heterologous priming-boosting with DNA and modified vaccinia virus Ankara expressing tryparedoxin peroxidase promotes long-term memory against Leishmania major in susceptible BALB/c MiceModulating vaccine responses with dendritic cells and Toll-like receptors.Vaccines that facilitate antigen entry into dendritic cells.Pathogen-imposed skewing of mouse chemokine and cytokine expression at the infected tissue siteCpG-matured murine plasmacytoid dendritic cells are capable of in vivo priming of functional CD8 T cell responses to endogenous but not exogenous antigens.The linkage of innate to adaptive immunity via maturing dendritic cells in vivo requires CD40 ligation in addition to antigen presentation and CD80/86 costimulationDNA-Salmonella enterica serovar Typhimurium primer-booster vaccination biases towards T helper 1 responses and enhances protection against Leishmania major infection in mice.Intranasal vaccination against cutaneous leishmaniasis with a particulated leishmanial antigen or DNA encoding LACK.Cutaneous Leishmania infection: progress in pathogenesis research and experimental therapy.Distinct roles for IL-6 and IL-12p40 in mediating protection against Leishmania donovani and the expansion of IL-10+ CD4+ T cells.Physiological role of plasmacytoid dendritic cells and their potential use in cancer immunity.Improved proliferation of antigen-specific cytolytic T lymphocytes using a multimodal nanovaccine.CpG plus radiotherapy: a review of preclinical works leading to clinical trial.Mechanisms of action of adjuvantsImmunogenic, but not steady-state, antigen presentation permits regulatory T-cells to control CD8+ T-cell effector differentiation by IL-2 modulation.Activated T cells express the OX40 ligand: requirements for induction and costimulatory function.Cross-talk between CD8(+) and CD4(+) T cells in experimental cutaneous leishmaniasis: CD8(+) T cells are required for optimal IFN-gamma production by CD4(+) T cells.
P2860
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P2860
Dendritic cells are responsible for the capacity of CpG oligodeoxynucleotides to act as an adjuvant for protective vaccine immunity against Leishmania major in mice
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年學術文章
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name
Dendritic cells are responsibl ...... ainst Leishmania major in mice
@ast
Dendritic cells are responsibl ...... ainst Leishmania major in mice
@en
type
label
Dendritic cells are responsibl ...... ainst Leishmania major in mice
@ast
Dendritic cells are responsibl ...... ainst Leishmania major in mice
@en
prefLabel
Dendritic cells are responsibl ...... ainst Leishmania major in mice
@ast
Dendritic cells are responsibl ...... ainst Leishmania major in mice
@en
P2093
P2860
P356
P1476
Dendritic cells are responsibl ...... ainst Leishmania major in mice
@en
P2093
Chang-You Wu
David R Ambrozak
Javeed A Shah
Joanna Kirman
Nicolas Glaichenhaus
Patricia A Darrah
Robert A Seder
Susana Mendez
Tara N Turon
P2860
P304
P356
10.1084/JEM.20030645
P407
P577
2003-07-01T00:00:00Z