2B4 Mediates Inhibition of CD8 + T Cell Responses via Attenuation of Glycolysis and Cell Division

• Published in: The Journal of immunology (1950) Vol. 201; no. 5; pp. 1536 - 1548
• Main Authors: Laurie, Sonia J, Liu, Danya, Wagener, Maylene E, Stark, Phoebe C, Terhorst, Cox, Ford, Mandy L
• Format: Journal Article
• Language: English
• Published: United States 01-09-2018
• Subjects: Animals; CD8-Positive T-Lymphocytes - immunology; Cell Division - genetics; Cell Division - immunology; Glycolysis - genetics; Glycolysis - immunology; Graft Survival - genetics; Graft Survival - immunology; Lymphocyte Activation; Mice; Mice, Knockout; Signal Transduction - genetics; Signal Transduction - immunology; Signaling Lymphocytic Activation Molecule Family - genetics; Signaling Lymphocytic Activation Molecule Family - immunology; Skin Transplantation
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1701240

We recently showed that 2B4 expression on memory T cells in human renal transplant recipients was associated with reduced rates of rejection. To investigate whether 2B4 functionally underlies graft acceptance during transplantation, we established an experimental model in which 2B4 was retrogenically expressed on donor-reactive murine CD8
T cells (2B4rg), which were then transferred into naive recipients prior to skin transplantation. We found that constitutive 2B4 expression resulted in significantly reduced accumulation of donor-reactive CD8
T cells following transplantation and significantly prolonged graft survival following transplantation. This marked reduction in alloreactivity was due to reduced proliferation of CD8
Thy1.1
2B4rg cells as compared with control cells, underpinned by extracellular flux analyses demonstrating that 2B4-deficient (2B4KO) CD8
cells activated in vitro exhibited increased glycolytic capacity and upregulation of gene expression profiles consistent with enhanced glycolytic machinery as compared with wild type controls. Furthermore, 2B4KO CD8
T cells primed in vivo exhibited significantly enhanced ex vivo uptake of a fluorescent glucose analogue. Finally, the proliferative advantage associated with 2B4 deficiency was only observed in the setting of glucose sufficiency; in glucose-poor conditions, 2B4KO CD8
T cells lost their proliferative advantage. Together, these data indicate that 2B4 signals function to alter T cell glucose metabolism, thereby limiting the proliferation and accumulation of CD8
T cells. Targeting 2B4 may therefore represent a novel therapeutic strategy to attenuate unwanted CD8
T cell responses.