Research in mice and non-human primates has demonstrated that costimulation-blockade resistant organ rejection following transplantation is primarily mediated by donor-reactive CD8+ T cells. Controlling these alloreactive T cell responses is imperative for improving long-term outcomes in pediatric and adult transplant recipients. The Ig-superfamily member 2B4 (SLAMf4, CD244) has been shown to be inducibly expressed on ??-CD8+ T cells. Our recent studies suggest that 2B4 plays a functional role in the inhibition of donor-reactive CD8+ T cell responses following CD28 costimulation blockade in vivo, raising the possibility that 2B4 itself could be a therapeutic target to attenuate allograft rejection. Preliminary data suggest that 2B4 may function as a costimulator during primary pathogen- specific CD8+ T cell activation and raise the exciting possibility that 2B4 could be specifically manipulated to attenuate acute graft rejection mediated by alloreactive CD8+ T cells following transplantation, while simultaneously maintaining functional immune responses capable of defending the host from pathogen infections. This work will test the concept that graft-specific and pathogen-specific CD8+ T cells express different complements of costimulatory and coinhibitory molecules. We propose that certain signaling pathways in T cells may be differentially engaged in the setting of infection and transplant and that these responses can be exploited to maximize protective immunity and minimize the risk of rejection following transplantation.

Public Health Relevance

The proposed research is relevant to public health because it characterizes expression and function of a cosignaling molecule that could be manipulated to attenuate alloreactive T cell responses following transplantation while maintaining protective immune responses against foreign pathogens. This contribution is relevant to NIH's mission in that it may facilitate the development of safe and effective immunosuppression for patients receiving solid organ transplants for the treatment of chronic liver, kidney, and lung diseases among others.

National Institute of Health (NIH)
National Institute of Allergy and Infectious Diseases (NIAID)
Predoctoral Individual National Research Service Award (F31)
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Special Emphasis Panel (ZRG1)
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Adger-Johnson, Diane S
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Emory University
Schools of Medicine
United States
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Laurie, Sonia J; Liu, Danya; Wagener, Maylene E et al. (2018) 2B4 Mediates Inhibition of CD8+ T Cell Responses via Attenuation of Glycolysis and Cell Division. J Immunol 201:1536-1548
Bozeman, Alana M; Laurie, Sonia J; Haridas, Divya et al. (2018) Transplantation preferentially induces a KLRG-1lo CD127hi differentiation program in antigen-specific CD8+ T cells. Transpl Immunol 50:34-42
Laurie, Sonia J; Ford, Mandy L (2017) Epigenetic Remodeling in Exhausted T Cells: Implications for Transplantation Tolerance. Transplantation 101:894-895
Cortes-Cerisuelo, M; Laurie, S J; Mathews, D V et al. (2017) Increased Pretransplant Frequency of CD28+ CD4+ TEM Predicts Belatacept-Resistant Rejection in Human Renal Transplant Recipients. Am J Transplant 17:2350-2362
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