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

Almut Brand ,
Katrin Singer ,
Gudrun E Koehl ,
Marlene Kolitzus ,
Gabriele Schoenhammer ,
Annette Thiel ,
Carina Matos ,
Christina Bruss ,
Sebastian Klobuch ,
Katrin Peter ,
Michael Kastenberger ,
Christian Bogdan ,
Ulrike Schleicher ,
Andreas Mackensen ,
Evelyn Ullrich ,
Stefan Fichtner-Feigl ,
Rebecca Kesselring ,
Matthias Mack ,
Uwe Ritter ,
Maximilian Schmid ,
Christian Blank ,
Katja Dettmer ,
Peter J Oefner ,
Petra Hoffmann ,
Stefan Walenta ,
Edward K Geissler ,
Jacques Pouyssegur ,
Andreas Villunger ,
André Steven ,
Barbara Seliger ,
Stephan Schreml ,
Sebastian Haferkamp ,
Elisabeth Kohl ,
Sigrid Karrer ,
Mark Berneburg ,
Wolfgang Herr ,
Wolfgang Mueller-Klieser ,
Kathrin Renner ,
Marina Kreutz

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 (Ldhalow) developed significantly slower than control tumors and showed increased infiltration with IFN-γ-producing T and NK cells. However, in Rag2-/-γc-/- mice, lacking lymphocytes and NK cells, and in Ifng-/- mice, Ldhalow 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.

More about this publication

Cell metabolism

Volume 24
Issue nr. 5
Pages 657-671
Publication date 08-11-2016

Full text links

Publisher website (DOI) 10.1016/j.cmet.2016.08.011
Europe PubMed Central 27641098
Pubmed 27641098

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