Cited by 49T-cell and B-cell ImmunologyImmune cells in cancerImmunotherapy and Immune Responses

Regulation of T-cell functions by l-lactate

Dröge, Wulf, Roth, Steffen, Altmann, Annette, Mihm, Sabine·1987·Cellular Immunology

Abstract

Lactate is a product of glycolytically active macrophages. After stimulation with concanavalin A accessory cell-depleted splenic T-cell populations were found to produce only minute amounts of T-cell growth factor (TCGF); but substantial amounts of TCGF were produced if the cultures were supplemented either with splenic adherent cells or with lactate but not with interleukin-1 (IL-1). IL-1 was capable, however, of supporting TCGF production by the thymoma subline EL4-6.1. TCGF production in cultures of accessory cell-depleted splenic T-cell populations was demonstrable with 10(-3) M L-lactate, and optimal responses (plateau level) were obtained with 4-6 X 10(-2) M L-lactate. Cultures of macrophages were found to accumulate up to 5 X 10(-2) M lactate. Our experiments indicate, therefore, that lactate serves as a regulatory signal by which macrophage-like accessory cells enhance helper-T-cell functions. Lactate is apparently not the only mediator of accessory cell function since plateau levels of TCGF production were markedly lower with lactate than with splenic accessory cells; but L-lactate was found also to determine the magnitude of T-cell-mediated immune responses in vivo and in cultures of unfractionated lymphocyte populations. The production of interferon in accessory cell-depleted and concanavalin A-treated T-cell cultures, however, was not significantly affected by lactate. Concanavalin A-stimulated splenic T-cell populations were found to consume glucose rapidly and t…

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Crossref · 10.1016/0008-8749(87)90223-1

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  • Cancer cells compete with immune cells for glucose uptake (by SLC2A1/GLUT1), produce lactic acid (by LDHA), and generate an acidic extracellular milieu (through the activity of CA9), all of which are immunosuppressive.

    “Cancer cells compete with immune cells for glucose uptake (by SLC2A1/GLUT1), produce lactic acid (by LDHA), and generate an acidic extracellular milieu (through the activity of CA9), all of which are immunosuppressive (77–86).”

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References 30 · Cited by 49

Authors
Dröge, W., Roth, S., Altmann, A., & Mihm, S.
Affiliations
German Cancer Research Center (DE)
Venue
Cellular Immunology
Publisher
Elsevier BV
Published
1987-09
Volume
108
Issue
2
Pages
405-416
ISSN
0008-8749 (ISSN-L)
OpenAlex
W1971587845
Cited by
49
References
30
Citations by year
2026: 2 · 2024: 1 · 2023: 1 · 2022: 2 · 2021: 2 · 2019: 1 · 2018: 5 · 2017: 1 · 2016: 5 · 2013: 2 · 2012: 2
FWCI
0.79
Type
journal article
Language
en
Open access
closed
Locations
  • Cellular Immunology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
Keywords
L-lactate, T cell activation, interleukin-2, T helper cells, concanavalin A, interleukin-1, splenic T cells, glucose metabolism, pyruvate, interferon, T cell immunity, glycolysis
MeSH terms
Animals, Antigen-Presenting Cells, Cells, Cultured, Cytotoxicity, Immunologic, Glucose, Immunologic Memory, Interleukin-2, Lactates, Lymph Nodes, Lymphocyte Activation, Macrophages, Pyruvates, Spleen, T-Lymphocytes, T-Lymphocytes, Cytotoxic, Lactic Acid, Mice, In Vitro Techniques

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