(Q52886319)

9 May 2018

title

The recombinant tuberculosis vaccine rBCG ΔureC::hly(+) induces apoptotic vesicles for improved priming of CD4(+) and CD8(+) T cells. (English)

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9 May 2018

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3

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9 May 2018

author name string

Maura Farinacci

series ordinal

1

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9 May 2018

Stephan Weber

series ordinal

2

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9 May 2018

language of work or name

English

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publication date

22 October 2012

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9 May 2018

published in

Vaccine

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9 May 2018

volume

30

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9 May 2018

issue

52

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9 May 2018

page(s)

7608-7614

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9 May 2018

Envisioning future strategies for vaccination against tuberculosis.

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Gamma interferon-producing CD4+ T lymphocytes in the lung correlate with resistance to infection with Mycobacterium tuberculosis.

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Apoptosis facilitates antigen presentation to T lymphocytes through MHC-I and CD1 in tuberculosis.

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Apoptotic vesicles crossprime CD8 T cells and protect against tuberculosis.

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CD40 triggering of heterodimeric IL-12 p70 production by dendritic cells in vivo requires a microbial priming signal

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Newly activated T cells promote maturation of bystander dendritic cells but not IL-12 production

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Inflammatory signals in dendritic cell activation and the induction of adaptive immunity

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7 January 2021

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7 January 2021

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7 January 2021

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Recombinant BCG ΔureC hly+ induces superior protection over parental BCG by stimulating a balanced combination of type 1 and type 17 cytokine responses

7 January 2021

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IL-6 programs T(H)-17 cell differentiation by promoting sequential engagement of the IL-21 and IL-23 pathways

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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10.1016/J.VACCINE.2012.10.031

7 January 2021

Identifiers

DOI

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9 May 2018

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9 May 2018