Author response for "Human liver‐derived MAIT cells differ from blood MAIT cells in their metabolism and response to TCR‐independent activation"

Author(s):  
Rajesh Lamichhane ◽  
Fran Munro ◽  
Thomas W. R. Harrop ◽  
Sara M. Harpe ◽  
Peter K. Dearden ◽  
...  
2020 ◽  
Vol 73 (3) ◽  
pp. 640-650 ◽  
Author(s):  
Min-Seok Rha ◽  
Ji Won Han ◽  
Jong Hoon Kim ◽  
June-Young Koh ◽  
Hye Jung Park ◽  
...  
Keyword(s):  

Author(s):  
Matty L. Terpstra ◽  
Ester B.M. Remmerswaal ◽  
Nelly D. der Bom‐Baylon ◽  
Marjan J. Sinnige ◽  
Jesper Kers ◽  
...  

Author(s):  
Matty L. Terpstra ◽  
Ester B.M. Remmerswaal ◽  
Nelly D. der Bom‐Baylon ◽  
Marjan J. Sinnige ◽  
Jesper Kers ◽  
...  

2018 ◽  
Vol 38 (01) ◽  
pp. 060-065 ◽  
Author(s):  
Fabian Bolte ◽  
Barbara Rehermann

AbstractThe broadening field of microbiome research has led to a substantial reappraisal of the gut–liver axis and its role in chronic liver disease. The liver is a central immunologic organ that is continuously exposed to food and microbial-derived antigens from the gastrointestinal tract. Mucosal-associated invariant T (MAIT) cells are enriched in the human liver and can be activated by inflammatory cytokines and microbial antigens. In chronic inflammatory liver disease, MAIT cells are depleted suggesting an impaired MAIT cell-dependent protection against bacterial infections.


2020 ◽  
Author(s):  
Shubhanshi Trivedi ◽  
Daniel Labuz ◽  
Cole P Anderson ◽  
Claudia V Araujo ◽  
Antoinette Blair ◽  
...  

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