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Inhibition of inositol kinase B controls acute and chronic graft-versus-host disease

  • Govindarajan Thangavelu
    ,
  • Jing Du
    ,
  • Katelyn G. Paz
    ,
  • Michael Loschi
    ,
  • Michael C. Zaiken
    ,
  • Ryan Flynn
  • University of Minnesota Twin Cities
    ,
  • Johns Hopkins University
    ,
  • University of Queensland
    ,
  • University of Pennsylvania
    ,
  • ,
  • University of North Carolina at Chapel Hill
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

T-cell activation releases inositol 1,4,5-trisphosphate (IP3), inducing cytoplasmic calcium (Ca21) influx. In turn, inositol 1,4,5-trisphosphate 3-kinase B (Itpkb) phosphorylates IP3 to negatively regulate and thereby tightly control Ca21 fluxes that are essential for mature T-cell activation and differentiation and protection from cell death. Itpkb pathway inhibition increases intracellular Ca21, induces apoptosis of activated T cells, and can control T-cell–mediated autoimmunity. In this study, we employed genetic and pharmacological approaches to inhibit Itpkb signaling as a means of controlling graft-versus-host disease (GVHD). Murine-induced, Itpkb-deleted (Itpkb2/2) T cells attenuated acute GVHD in 2 models without eliminating A20-luciferase B-cell lymphoma graft-versus-leukemia (GVL). A highly potent, selective inhibitor, GNF362, ameliorated acute GVHD without impairing GVL against 2 acute myeloid leukemia lines (MLL-AF9-eGFP and C1498-luciferase). Compared with FK506, GNF362 more selectively deleted donor alloreactive vs nominal antigen-responsive T cells. Consistent with these data and as compared with FK506, GNF362 had favorable acute GVHD and GVL properties against MLL-AF9-eGFP cells. In chronic GVHD preclinical models that have a pathophysiology distinct from acute GVHD, Itpkb2/2 donor T cells reduced active chronic GVHD in a multiorgan system model of bronchiolitis obliterans (BO), driven by germinal center reactions and resulting in target organ fibrosis. GNF362 treatment reduced active chronic GVHD in both BO and scleroderma models. Thus, intact Itpkb signaling is essential to drive acute GVHD pathogenesis and sustain active chronic GVHD, pointing toward a novel clinical application to prevent acute or treat chronic GVHD.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 28-40 (13 pages)

Journal (Volume, Issue Number)

Blood (Volume 135, Issue 1)

Publication milestones

  • Published - 2020

Publication status

Published - 2020

ISSN

0006-4971

Publication IDs

  • Scopus: 85077477653
  • PubMed: 31697815
  • ORCID: /0000-0002-7711-2858/work/68451345

Publication metrics

Metrics

SciVal
FWCI
0.57
SciVal
Author count
25
SciVal
citations
2
SciVal
Paper percentile
78
Fractional count
1
Fractional count
0.04
Fractional count
24
Fractional count
0.96
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
32
Citation count
19

Funding Details

Conflict-of-interest disclosure: C.D. and A.T.M. are employees of The Novartis Institute for Biomedical Research. J.R. received research funding from Equillium and Kite Pharma and consulting income from Celgene, Avrobio, LifeVault Bio, Draper Labs, and TScan Therapeutics. B.R.B. receives remuneration as an advisor to Kamon Pharmaceuticals, Five Prime Therapeutics, Regeneron Pharmaceuticals, Magenta Therapeutics, and BlueRock Therapeuetics; research support from Fate Therapeutics, RXi Pharmaceuticals, Alpine Immune Sciences, Abbvie, the Leukemia and Lymphoma Society, the Children’s Cancer Research Fund, and the KidsFirst Fund and is a cofounder of Tmunity. The remaining authors declare no competing financial interests. This work was supported by National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases grants P01AI056299 and R01AI034495 (B.R.B.) and grant R01AI091627 (I.M.); NIH National Heart, Lung, and Blood Institute grant R01HL56067 (B.R.B.); and NIH National Cancer Institute grant P01CA142106 (B.R.B., D.M., C.S.C., J.K., J.H.A., R.J.S., J.R.); a Leukemia and Lymphoma Society-Translational Research Program (LLS-TRP) award (I.M., B.R.B.); and a Canadian Institutes of Health Research (CIHR) fellowship (G.T.). The authors thank Jamie Panthera for expert mouse husbandry and care. This work was supported by National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases grants P01AI056299 and R01AI034495 (B.R.B.) and grant R01AI091627 (I.M.); NIH National Heart, Lung, and Blood Institute grant R01HL56067 (B.R.B.); and NIH National Cancer Institute grant P01CA142106 (B.R.B., D.M., C.S.C., J.K., J.H.A., R.J.S., J.R.); a Leukemia and Lymphoma Society-Translational Research Program (LLS-TRP) award (I.M., B.R.B.); and a Canadian Institutes of Health Research (CIHR) fellowship (G.T.).
FundersFunding numbers
Tmunity
-
Leukemia and Lymphoma Society-Translational Research Program
-
Fate Therapeutics
-
NIH
-
Children's Cancer Research Fund
-
Magenta Therapeutics
-
CIHR
-
Celgene
-
LLS
-
NCI
R01CA103320, R01CA211229, P01CA142106
NIAID
R37AI034495, T32AI007313, R01AI091627, P01AI056299
NHLBI
R01HL118979, R01HL056067