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Multiple layers of heterogeneity and subset diversity in human MAIT cell responses to distinct microorganisms and to innate cytokines

Proceedings of the National Academy of Sciences - PNAS, 2017-07, Vol.114 (27), p.E5434-E5443

2017

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Acquisition of innate-like microbial reactivity in mucosal tissues during human fetal MAIT-cell development

Nature communications, 2014-01, Vol.5 (1), p.3143-3143, Article 3143

2014

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MAIT cells reside in the female genital mucosa and are biased towards IL-17 and IL-22 production in response to bacterial stimulation

Mucosal immunology, 2017, Vol.10 (1), p.35-45

2017

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Nonreversible MAIT cell‐dysfunction in chronic hepatitis C virus infection despite successful interferon‐free therapy

European journal of immunology, 2016-09, Vol.46 (9), p.2204-2210

2016

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Arming of MAIT Cell Cytolytic Antimicrobial Activity Is Induced by IL-7 and Defective in HIV-1 Infection

PLoS pathogens, 2015-08, Vol.11 (8), p.e1005072-e1005072

2015

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The CD4⁻CD8⁻ MAIT cell subpopulation is a functionally distinct subset developmentally related to the main CD8⁺ MAIT cell pool

Proceedings of the National Academy of Sciences - PNAS, 2018-12, Vol.115 (49), p.E11513-E11522

2018

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Evaluation of mucosal-associated invariant T-cells as a potential biomarker to predict infection risk in liver cirrhosis

PloS one, 2024-05, Vol.19 (5), p.e0294695-e0294695

2024

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Activation, exhaustion, and persistent decline of the antimicrobial MR1-restricted MAIT-cell population in chronic HIV-1 infection

Blood, 2013-02, Vol.121 (7), p.1124-1135

2013

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Prion propagation and toxicity in vivo occur in two distinct mechanistic phases

Nature (London), 2011-02, Vol.470 (7335), p.540-542

2011

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Ancestral SARS-CoV-2-specific T cells cross-recognize the Omicron variant

Nature medicine, 2022-03, Vol.28 (3), p.472-476

2022

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Bacterial deception of MAIT cells in a cloud of superantigen and cytokines

PLoS biology, 2017-07, Vol.15 (7), p.e2003167

2017

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Compromised Function of Natural Killer Cells in Acute and Chronic Viral Hepatitis

The Journal of infectious diseases, 2014-05, Vol.209 (9), p.1362-1373

2014

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Proteome analysis of human CD56neg NK cells reveals a homogeneous phenotype surprisingly similar to CD56dim NK cells

European journal of immunology, 2018-09, Vol.48 (9), p.1456-1469

2018

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Emerging Role for MAIT Cells in Control of Antimicrobial Resistance

Trends in microbiology (Regular ed.), 2021-06, Vol.29 (6), p.504-516

2021

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Cell-Mediated Immune Responses and Immunopathogenesis of Human Tick-Borne Encephalitis Virus-Infection

Frontiers in immunology, 2018-09, Vol.9, p.2174-2174

2018

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Chronic hepatitis delta virus infection leads to functional impairment and severe loss of MAIT cells

Journal of hepatology, 2019-08, Vol.71 (2), p.301-312

2019

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MAIT cell counts are associated with the risk of hospitalization in COPD

Respiratory research, 2022-05, Vol.23 (1), p.127-127, Article 127

2022

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NKG2D performs two functions in invariant NKT cells: Direct TCR‐independent activation of NK‐like cytolysis and co‐stimulation of activation by CD1d

European journal of immunology, 2011-07, Vol.41 (7), p.1913-1923

2011

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Recruitment of MAIT Cells to the Intervillous Space of the Placenta by Placenta-Derived Chemokines

Frontiers in immunology, 2019, Vol.10, p.1300-1300

2019

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Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked

Nature communications, 2014-07, Vol.5 (1), p.4347, Article 4347

2014

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CD56 negative NK cells: origin, function, and role in chronic viral disease

Trends in immunology, 2010-11, Vol.31 (11), p.401-406

2010

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MAIT Cells Are Major Contributors to the Cytokine Response in Group A Streptococcal Toxic Shock Syndrome

Proceedings of the National Academy of Sciences - PNAS, 2019-12, Vol.116 (51), p.25923-25931

2019

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High Levels of Chronic Immune Activation in the T-Cell Compartments of Patients Coinfected with Hepatitis C Virus and Human Immunodeficiency Virus Type 1 and on Highly Active Antiretroviral Therapy Are Reverted by Alpha Interferon and Ribavirin Treatment

Journal of Virology, 2009-11, Vol.83 (21), p.11407-11411

2009

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Automated segmentation and quantification of liver and spleen from CT images using normalized probabilistic atlases and enhancement estimation

Medical physics (Lancaster), 2010-02, Vol.37 (2), p.771-783

2010

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The Emerging Role of MAIT Cell Responses in Viral Infections

The Journal of immunology (1950), 2023-08, Vol.211 (4), p.511

2023

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Multiple layers of heterogeneity and subset diversity in human MAIT cell responses to distinct microorganisms and to innate cytokines

Acquisition of innate-like microbial reactivity in mucosal tissues during human fetal MAIT-cell development

MAIT cells reside in the female genital mucosa and are biased towards IL-17 and IL-22 production in response to bacterial stimulation

Nonreversible MAIT cell‐dysfunction in chronic hepatitis C virus infection despite successful interferon‐free therapy

Arming of MAIT Cell Cytolytic Antimicrobial Activity Is Induced by IL-7 and Defective in HIV-1 Infection

The CD4⁻CD8⁻ MAIT cell subpopulation is a functionally distinct subset developmentally related to the main CD8⁺ MAIT cell pool

Evaluation of mucosal-associated invariant T-cells as a potential biomarker to predict infection risk in liver cirrhosis

Activation, exhaustion, and persistent decline of the antimicrobial MR1-restricted MAIT-cell population in chronic HIV-1 infection

Prion propagation and toxicity in vivo occur in two distinct mechanistic phases

Ancestral SARS-CoV-2-specific T cells cross-recognize the Omicron variant

Bacterial deception of MAIT cells in a cloud of superantigen and cytokines

Compromised Function of Natural Killer Cells in Acute and Chronic Viral Hepatitis

Proteome analysis of human CD56neg NK cells reveals a homogeneous phenotype surprisingly similar to CD56dim NK cells

Emerging Role for MAIT Cells in Control of Antimicrobial Resistance

Cell-Mediated Immune Responses and Immunopathogenesis of Human Tick-Borne Encephalitis Virus-Infection

Chronic hepatitis delta virus infection leads to functional impairment and severe loss of MAIT cells

MAIT cell counts are associated with the risk of hospitalization in COPD

NKG2D performs two functions in invariant NKT cells: Direct TCR‐independent activation of NK‐like cytolysis and co‐stimulation of activation by CD1d

Recruitment of MAIT Cells to the Intervillous Space of the Placenta by Placenta-Derived Chemokines

Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked

CD56 negative NK cells: origin, function, and role in chronic viral disease

MAIT Cells Are Major Contributors to the Cytokine Response in Group A Streptococcal Toxic Shock Syndrome

High Levels of Chronic Immune Activation in the T-Cell Compartments of Patients Coinfected with Hepatitis C Virus and Human Immunodeficiency Virus Type 1 and on Highly Active Antiretroviral Therapy Are Reverted by Alpha Interferon and Ribavirin Treatment

Automated segmentation and quantification of liver and spleen from CT images using normalized probabilistic atlases and enhancement estimation

The Emerging Role of MAIT Cell Responses in Viral Infections

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