CD11c+ antigen presenting cells from the alveolar space, lung parenchyma and spleen differ in their phenotype and capabilities to activate naïve and antigen-primed T cells.
about
Intranasal mucosal boosting with an adenovirus-vectored vaccine markedly enhances the protection of BCG-primed guinea pigs against pulmonary tuberculosis.IL-36α exerts pro-inflammatory effects in the lungs of micePulmonary mycobacterial granuloma increased IL-10 production contributes to establishing a symbiotic host-microbe microenvironment.Asymptomatic HIV-infected individuals on antiretroviral therapy exhibit impaired lung CD4(+) T-cell responses to mycobacteria.Modulation of the immune response to respiratory viruses by vitamin D.Virus-like particle-induced protection against MRSA pneumonia is dependent on IL-13 and enhancement of phagocyte function.Participation of Tumor-Associated Myeloid Cells in Progression of Amelanotic Melanoma (RMM Tumor Line) in F344 Rats, with Particular Reference to MHC Class II- and CD163-Expressing Cells.Alveolar epithelial cells are critical in protection of the respiratory tract by secretion of factors able to modulate the activity of pulmonary macrophages and directly control bacterial growth.An innovative approach to induce cross-protective immunity against porcine reproductive and respiratory syndrome virus in the lungs of pigs through adjuvanted nanotechnology-based vaccination.Diverse macrophage populations mediate acute lung inflammation and resolution.Understanding delayed T-cell priming, lung recruitment, and airway luminal T-cell responses in host defense against pulmonary tuberculosis.Pulmonary M. tuberculosis infection delays Th1 immunity via immunoadaptor DAP12-regulated IRAK-M and IL-10 expression in antigen-presenting cells.Differentially imprinted innate immunity by mucosal boost vaccination determines antituberculosis immune protective outcomes, independent of T-cell immunity.RGD capsid modification enhances mucosal protective immunity of a non-human primate adenovirus vector expressing Pseudomonas aeruginosa OprF.Murine airway luminal antituberculosis memory CD8 T cells by mucosal immunization are maintained via antigen-driven in situ proliferation, independent of peripheral T cell recruitment.
P2860
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P2860
CD11c+ antigen presenting cells from the alveolar space, lung parenchyma and spleen differ in their phenotype and capabilities to activate naïve and antigen-primed T cells.
description
2008 nî lūn-bûn
@nan
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
CD11c+ antigen presenting cell ...... ve and antigen-primed T cells.
@ast
CD11c+ antigen presenting cell ...... ve and antigen-primed T cells.
@en
type
label
CD11c+ antigen presenting cell ...... ve and antigen-primed T cells.
@ast
CD11c+ antigen presenting cell ...... ve and antigen-primed T cells.
@en
prefLabel
CD11c+ antigen presenting cell ...... ve and antigen-primed T cells.
@ast
CD11c+ antigen presenting cell ...... ve and antigen-primed T cells.
@en
P2093
P2860
P356
P1433
P1476
CD11c+ antigen presenting cell ...... ve and antigen-primed T cells.
@en
P2093
Cherrie-Lee Small
Elizabeth K Roediger
Kapilan Kugathasan
Pingchang Yang
Sarah McCormick
P2860
P2888
P356
10.1186/1471-2172-9-48
P577
2008-08-13T00:00:00Z
P5875
P6179
1008040249