2. Academic Validation
  3. Targeting Aurora kinase A and JAK2 prevents GVHD while maintaining Treg and antitumor CTL function

Targeting Aurora kinase A and JAK2 prevents GVHD while maintaining Treg and antitumor CTL function

  • Sci Transl Med. 2017 Jan 11;9(372):eaai8269. doi: 10.1126/scitranslmed.aai8269.
Brian C Betts 1 2 3,  Anandharaman Veerapathran 4 2,  Joseph Pidala 4 2 3,  Hua Yang 3,  Pedro Horna 3 5,  Kelly Walton 2,  Christopher L Cubitt 6,  Steven Gunawan 3,  Harshani R Lawrence 3 7,  Nicholas J Lawrence 3 7,  Said M Sebti 3 7,  Claudio Anasetti 4 2 3
Affiliations

Affiliations

  • 1 Department of Blood and Marrow Transplantation, Moffitt Cancer Center, Tampa, FL 33612, USA. brian.betts@moffitt.org.
  • 2 Department of Immunology, Moffitt Cancer Center, Tampa, FL 33612, USA.
  • 3 Department of Oncologic Sciences, University of South Florida, Tampa, FL 33612, USA.
  • 4 Department of Blood and Marrow Transplantation, Moffitt Cancer Center, Tampa, FL 33612, USA.
  • 5 Department of Hematopathology and Laboratory Medicine, Moffitt Cancer Center, Tampa, FL 33612, USA.
  • 6 Translational Research Core, Moffitt Cancer Center, Tampa, FL 33612, USA.
  • 7 Department of Drug Discovery, Moffitt Cancer Center, Tampa, FL 33612, USA.
PMID: 28077684 DOI: 10.1126/scitranslmed.aai8269
Abstract

Graft-versus-host disease (GVHD) is a leading cause of nonrelapse mortality after allogeneic hematopoietic cell transplantation. T cell costimulation by CD28 contributes to GVHD, but prevention is incomplete when targeting CD28, downstream mammalian target of rapamycin (mTOR), or Aurora A. Likewise, interleukin-6 (IL-6)-mediated Janus kinase 2 (JAK2) signaling promotes alloreactivity, yet JAK2 inhibition does not eliminate GVHD. We provide evidence that blocking Aurora A and JAK2 in human T cells is synergistic in vitro, prevents xenogeneic GVHD, and maintains antitumor responses by cytotoxic T lymphocytes (CTLs). Aurora A/JAK2 inhibition is immunosuppressive but permits the differentiation of inducible regulatory T cells (iTregs) that are hyperfunctional and CD39 bright and efficiently scavenge adenosine triphosphate (ATP). Increased iTreg potency is primarily a function of Aurora A blockade, whereas JAK2 inhibition suppresses T helper 17 (TH17) differentiation. Inhibiting either Aurora A or JAK2 significantly suppresses TH1 T cells. However, CTL generated in vivo retains tumor-specific killing despite Aurora A/JAK2 blockade. Thus, inhibiting CD28 and IL-6 signal transduction pathways in donor T cells can increase the Treg/Tconv ratio, prevent GVHD, and preserve antitumor CTL.

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