Differentially imprinted innate immunity by mucosal boost vaccination determines antituberculosis immune protective outcomes, independent of T-cell immunity. (Q43514266)

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English	Differentially imprinted innate immunity by mucosal boost vaccination determines antituberculosis immune protective outcomes, independent of T-cell immunity.	scientific article

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17 February 2020

Differentially imprinted innate immunity by mucosal boost vaccination determines antituberculosis immune protective outcomes, independent of T-cell immunity (English)

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17 February 2020

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17 February 2020

author name string

M Jeyanathan

1

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17 February 2020

D Damjanovic

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17 February 2020

C R Shaler

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M Wortzman

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C Yin

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A Zganiacz

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B D Lichty

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17 February 2020

Z Xing

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publication date

7 November 2012

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17 February 2020

Mucosal Immunology

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17 February 2020

6

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17 February 2020

3

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17 February 2020

612-625

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17 February 2020

https://scigraph.springernature.com/pub.10.1038/mi.2012.103

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Strategies and implications for prime-boost vaccination to generate memory CD8 T cells.

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Recent advances in the development of adenovirus- and poxvirus-vectored tuberculosis vaccines.

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Prime-boost immunization with poxvirus or adenovirus vectors as a strategy to develop a protective vaccine for HIV-1.

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Mucosal immunity and vaccines

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Genetic heterologous prime-boost vaccination strategies for improved systemic and mucosal immunity

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What role does the route of immunization play in the generation of protective immunity against mucosal pathogens?

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Mucosal vaccination overcomes the barrier to recombinant vaccinia immunization caused by preexisting poxvirus immunity

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Nasal delivery of an adenovirus-based vaccine bypasses pre-existing immunity to the vaccine carrier and improves the immune response in mice

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T cells in mycobacterial infection and disease

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T-cell quality in memory and protection: implications for vaccine design

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Initiation and regulation of T-cell responses in tuberculosis

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Tuberculosis vaccine research: the impact of immunology

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Immunological outcomes of new tuberculosis vaccine trials: WHO panel recommendations

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Intranasal Poly-IC treatment exacerbates tuberculosis in mice through the pulmonary recruitment of a pathogen-permissive monocyte/macrophage population

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Preexisting helminth infection induces inhibition of innate pulmonary anti-tuberculosis defense by engaging the IL-4 receptor pathway

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Understanding delayed T-cell priming, lung recruitment, and airway luminal T-cell responses in host defense against pulmonary tuberculosis

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TNF-alpha is a critical negative regulator of type 1 immune activation during intracellular bacterial infection

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Immunogenicity of recombinant adenovirus serotype 35 vaccine in the presence of pre-existing anti-Ad5 immunity.

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Comparative Immunogenicity in Rhesus Monkeys of DNA Plasmid, Recombinant Vaccinia Virus, and Replication-Defective Adenovirus Vectors Expressing a Human Immunodeficiency Virus Type 1 gag Gene

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Replication-incompetent adenoviral vaccine vector elicits effective anti-immunodeficiency-virus immunity

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Mechanisms of mucosal and parenteral tuberculosis vaccinations: adenoviral-based mucosal immunization preferentially elicits sustained accumulation of immune protective CD4 and CD8 T cells within the airway lumen.

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Heterologous boosting of recombinant adenoviral prime immunization with a novel vesicular stomatitis virus-vectored tuberculosis vaccine

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Fatal Mycobacterium tuberculosis infection despite adaptive immune response in the absence of MyD88.

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Role of innate cytokines in mycobacterial infection.

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Macrophages are a significant source of type 1 cytokines during mycobacterial infection

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Interferon-alpha/beta inhibition of interleukin 12 and interferon-gamma production in vitro and endogenously during viral infection

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Induction of IFN-alphabeta enables Listeria monocytogenes to suppress macrophage activation by IFN-gamma

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Use of recombinant virus-vectored tuberculosis vaccines for respiratory mucosal immunization

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Progression of pulmonary tuberculosis and efficiency of bacillus Calmette-Guérin vaccination are genetically controlled via a common sst1-mediated mechanism of innate immunity.

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A comparison of IFNgamma detection methods used in tuberculosis vaccine trials

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Single mucosal, but not parenteral, immunization with recombinant adenoviral-based vaccine provides potent protection from pulmonary tuberculosis

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Pulmonary mucosal dendritic cells in T-cell activation: implications for TB therapy

1 reference

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7 January 2021

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10.1038/MI.2012.103

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17 February 2020

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17 February 2020

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