STING and transplantation: can targeting this pathway improve outcomes?

Author:

Bader Cameron S.1ORCID,Jin Lei2ORCID,Levy Robert B.13ORCID

Affiliation:

1. Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL;

2. Department of Medicine, Division of Pulmonary Critical Care and Sleep Medicine, University of Florida College of Medicine, Gainesville, FL; and

3. Sylvester Comprehensive Cancer Center, Department of Medicine and Department of Ophthalmology, University of Miami Miller School of Medicine, Miami, FL

Abstract

Abstract Stimulator of interferon genes (STING) is an innate immune sensor of cytoplasmic dsDNA originating from microorganisms and host cells. STING plays an important role in the regulation of murine graft-versus-host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (allo-HSCT) and may be similarly activated during other transplantation modalities. In this review, we discuss STING in allo-HSCT and its prospective involvement in autologous HSCT (auto-HSCT) and solid organ transplantation (SOT), highlighting its unique role in nonhematopoietic, hematopoietic, and malignant cell types.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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