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T-cells produce acidic niches in lymph nodes to suppress their own effector functions

Author

Listed:
  • Hao Wu

    (H. Lee Moffitt Cancer Center and Research Institute
    Zhejiang University School of Medicine)

  • Veronica Estrella

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Matthew Beatty

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Dominique Abrahams

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Asmaa El-Kenawi

    (H. Lee Moffitt Cancer Center and Research Institute
    H. Lee Moffitt Cancer Center and Research Institute)

  • Shonagh Russell

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Arig Ibrahim-Hashim

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Dario Livio Longo

    (National Research Council of Italy (CNR))

  • Yana K. Reshetnyak

    (University of Rhode Island)

  • Anna Moshnikova

    (University of Rhode Island)

  • Oleg A. Andreev

    (University of Rhode Island)

  • Kimberly Luddy

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Mehdi Damaghi

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Krithika Kodumudi

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Smitha R. Pillai

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Pedro Enriquez-Navas

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Shari Pilon-Thomas

    (H. Lee Moffitt Cancer Center and Research Institute)

  • Pawel Swietach

    (University of Oxford)

  • Robert J. Gillies

    (H. Lee Moffitt Cancer Center and Research Institute)

Abstract

The acidic pH of tumors profoundly inhibits effector functions of activated CD8 + T-cells. We hypothesize that this is a physiological process in immune regulation, and that it occurs within lymph nodes (LNs), which are likely acidic because of low convective flow and high glucose metabolism. Here we show by in vivo fluorescence and MR imaging, that LN paracortical zones are profoundly acidic. These acidic niches are absent in athymic Nu/Nu and lymphodepleted mice, implicating T-cells in the acidifying process. T-cell glycolysis is inhibited at the low pH observed in LNs. We show that this is due to acid inhibition of monocarboxylate transporters (MCTs), resulting in a negative feedback on glycolytic rate. Importantly, we demonstrate that this acid pH does not hinder initial activation of naïve T-cells by dendritic cells. Thus, we describe an acidic niche within the immune system, and demonstrate its physiological role in regulating T-cell activation.

Suggested Citation

  • Hao Wu & Veronica Estrella & Matthew Beatty & Dominique Abrahams & Asmaa El-Kenawi & Shonagh Russell & Arig Ibrahim-Hashim & Dario Livio Longo & Yana K. Reshetnyak & Anna Moshnikova & Oleg A. Andreev , 2020. "T-cells produce acidic niches in lymph nodes to suppress their own effector functions," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17756-7
    DOI: 10.1038/s41467-020-17756-7
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    Cited by:

    1. Thomas Thisted & F. Donelson Smith & Arnab Mukherjee & Yuliya Kleschenko & Feng Feng & Zhi-Gang Jiang & Timothy Eitas & Kanam Malhotra & Zuzana Biesova & Adejumoke Onumajuru & Faith Finley & Anokhi Ci, 2024. "VISTA checkpoint inhibition by pH-selective antibody SNS-101 with optimized safety and pharmacokinetic profiles enhances PD-1 response," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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