Danger-associated extracellular ATP counters MDSC therapeutic efficacy in acute GVHD
- Brent H. Koehn,
- Asim Saha,
- Cameron McDonald-Hyman,
- Michael Loschi,
- Govindarajan Thangavelu,
- Lie Ma
- University of Minnesota Twin Cities,
- University of Queensland,
- Novartis,
- Kanazawa Medical University,
- University of North Carolina at Chapel Hill,
- University of California at Davis
Open access
Abstract
Myeloid-derived suppressor cells (MDSCs) can subdue inflammation. In mice with acute graft-versus-host disease (GVHD), donor MDSC infusion enhances survival that is only partial and transient because of MDSC inflammasome activation early posttransfer, resulting in differentiation and loss of suppressor function. Here we demonstrate that conditioning regimen-induced adenosine triphosphate (ATP) release is a primary driver of MDSC dysfunction through ATP receptor (P2x7R) engagement and NLR pyrin family domain 3 (NLRP3) inflammasome activation. P2x7R or NLRP3 knockout (KO) donor MDSCs provided significantly higher survival than wild-type (WT) MDSCs. Although in vivo pharmacologic targeting of NLRP3 or P2x7R promoted recipient survival, indicating in vivo biologic effects, no synergistic survival advantage was seen when combined with MDSCs. Because activated inflammasomes release mature interleukin-1β (IL-1β), we expected that IL-1β KO donor MDSCs would be superior in subverting GVHD, but such MDSCs proved inferior relative to WT. IL-1β release and IL-1 receptor expression was required for optimal MDSC function, and exogenous IL-1β added to suppression assays that included MDSCs increased suppressor potency. These data indicate that prolonged systemic NLRP3 inflammasome inhibition and decreased IL-1β could diminish survival in GVHD. However, loss of inflammasome activation and IL-1β release restricted to MDSCs rather than systemic inhibition allowed non-MDSC IL-1β signaling, improving survival. Extracellular ATP catalysis with peritransplant apyrase administered into the peritoneum, the ATP release site, synergized with WT MDSCs, as did regulatory T-cell infusion, which we showed reduced but did not eliminate MDSC inflammasome activation, as assessed with a novel inflammasome reporter strain. These findings will inform future clinical using MDSCs to decrease alloresponses in inflammatory environments.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 1670-1682 (13 pages)Journal (Volume, Issue Number)
Blood (Volume 134, Issue 19)Publication milestones
- Published - 11/07/2019
Publication status
ISSN
0006-4971Publication IDs
- Scopus: 85074676809
- PubMed: 31533918
- ORCID: /0000-0002-7711-2858/work/68451343
