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LDHA-Associated Lactic Acid Production Blunts Tumor Immunosurveillance by T and NK Cells.

Authors :
Brand A
Singer K
Koehl GE
Kolitzus M
Schoenhammer G
Thiel A
Matos C
Bruss C
Klobuch S
Peter K
Kastenberger M
Bogdan C
Schleicher U
Mackensen A
Ullrich E
Fichtner-Feigl S
Kesselring R
Mack M
Ritter U
Schmid M
Blank C
Dettmer K
Oefner PJ
Hoffmann P
Walenta S
Geissler EK
Pouyssegur J
Villunger A
Steven A
Seliger B
Schreml S
Haferkamp S
Kohl E
Karrer S
Berneburg M
Herr W
Mueller-Klieser W
Renner K
Kreutz M
Source :
Cell metabolism [Cell Metab] 2016 Nov 08; Vol. 24 (5), pp. 657-671. Date of Electronic Publication: 2016 Sep 15.
Publication Year :
2016

Abstract

Elevated lactate dehydrogenase A (LDHA) expression is associated with poor outcome in tumor patients. Here we show that LDHA-associated lactic acid accumulation in melanomas inhibits tumor surveillance by T and NK cells. In immunocompetent C57BL/6 mice, tumors with reduced lactic acid production (Ldha <superscript>low</superscript> ) developed significantly slower than control tumors and showed increased infiltration with IFN-γ-producing T and NK cells. However, in Rag2 <superscript>-/-</superscript> γc <superscript>-/-</superscript> mice, lacking lymphocytes and NK cells, and in Ifng <superscript>-/-</superscript> mice, Ldha <superscript>low</superscript> and control cells formed tumors at similar rates. Pathophysiological concentrations of lactic acid prevented upregulation of nuclear factor of activated T cells (NFAT) in T and NK cells, resulting in diminished IFN-γ production. Database analyses revealed negative correlations between LDHA expression and T cell activation markers in human melanoma patients. Our results demonstrate that lactic acid is a potent inhibitor of function and survival of T and NK cells leading to tumor immune escape.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1932-7420
Volume :
24
Issue :
5
Database :
MEDLINE
Journal :
Cell metabolism
Publication Type :
Academic Journal
Accession number :
27641098
Full Text :
https://doi.org/10.1016/j.cmet.2016.08.011