Illuminating T cell-dendritic cell interactions in vivo by FlAsHing antigens
Munir Akkaya,
Jafar Al Souz,
Daniel Williams,
Rahul Kamdar,
Olena Kamenyeva,
Juraj Kabat,
Ethan Shevach,
Billur Akkaya
Affiliations
Munir Akkaya
Department of Internal Medicine, Division of Rheumatology and Immunology, The College of Medicine, The Ohio State University, Columbus, United States; Microbial Infection and Immunity, The Ohio State University Wexner Medical Center, Columbus, United States; Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, United States
Jafar Al Souz
National Institute of Allergy and Infectious Diseases, Bethesda, United States
Daniel Williams
National Institute of Allergy and Infectious Diseases, Bethesda, United States
Rahul Kamdar
National Institute of Allergy and Infectious Diseases, Bethesda, United States
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, United States; Department of Neurology, The Ohio State University Wexner Medical Center, Columbus, United States
Delineating the complex network of interactions between antigen-specific T cells and antigen presenting cells (APCs) is crucial for effective precision therapies against cancer, chronic infections, and autoimmunity. However, the existing arsenal for examining antigen-specific T cell interactions is restricted to a select few antigen-T cell receptor pairs, with limited in situ utility. This lack of versatility is largely due to the disruptive effects of reagents on the immune synapse, which hinder real-time monitoring of antigen-specific interactions. To address this limitation, we have developed a novel and versatile immune monitoring strategy by adding a short cysteine-rich tag to antigenic peptides that emits fluorescence upon binding to thiol-reactive biarsenical hairpin compounds. Our findings demonstrate the specificity and durability of the novel antigen-targeting probes during dynamic immune monitoring in vitro and in vivo. This strategy opens new avenues for biological validation of T-cell receptors with newly identified epitopes by revealing the behavior of previously unrecognized antigen-receptor pairs, expanding our understanding of T cell responses.