Mycobacterium tuberculosis ESX-1 system-secreted protein ESAT-6 but not CFP10 inhibits human T-cell immune responses (Q28487342)

24 January 2017

title

Mycobacterium tuberculosis ESX-1 system-secreted protein ESAT-6 but not CFP10 inhibits human T-cell immune responses (English)

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Mycobacterium tuberculosis

24 January 2017

main subject

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Buka Samten

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24 January 2017

Xisheng Wang

series ordinal

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24 January 2017

Peter F. Barnes

series ordinal

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24 January 2017

publication date

1 December 2009

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24 January 2017

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24 January 2017

volume

89 Suppl 1

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24 January 2017

page(s)

S74–76

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Evidence for occurrence of the ESAT-6 protein in Mycobacterium tuberculosis and virulent Mycobacterium bovis and for its absence in Mycobacterium bovis BCG.

24 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

A Mycobacterium tuberculosis operon encoding ESAT-6 and a novel low-molecular-mass culture filtrate protein (CFP-10)

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

ESAT-6 proteins: protective antigens and virulence factors?

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Systematic review: T-cell-based assays for the diagnosis of latent tuberculosis infection: an update

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Molecular analysis of genetic differences between Mycobacterium bovis BCG and virulent M. bovis

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Conclusive evidence that the major T-cell antigens of the Mycobacterium tuberculosis complex ESAT-6 and CFP-10 form a tight, 1:1 complex and characterization of the structural properties of ESAT-6, CFP-10, and the ESAT-6*CFP-10 complex. Implications

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Individual RD1-region genes are required for export of ESAT-6/CFP-10 and for virulence of Mycobacterium tuberculosis

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

The primary mechanism of attenuation of bacillus Calmette-Guerin is a loss of secreted lytic function required for invasion of lung interstitial tissue

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Acute infection and macrophage subversion by Mycobacterium tuberculosis require a specialized secretion system

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

The Type I IFN response to infection with Mycobacterium tuberculosis requires ESX-1-mediated secretion and contributes to pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Direct extracellular interaction between the early secreted antigen ESAT-6 of Mycobacterium tuberculosis and TLR2 inhibits TLR signaling in macrophages

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

ESAT-6 inhibits production of IFN-gamma by Mycobacterium tuberculosis-responsive human T cells

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Cyclic AMP response element-binding protein positively regulates production of IFN-gamma by T cells in response to a microbial pathogen

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

CREB, ATF, and AP-1 transcription factors regulate IFN-gamma secretion by human T cells in response to mycobacterial antigen

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

Complex complexes: signaling at the TCR.

1 reference

https://api.crossref.org/works/10.1016%2FS1472-9792%2809%2970017-4

7 January 2021

10.1016/S1472-9792(09)70017-4

Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017