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ReportsDifferent T Cell Receptor Signals Determine CD8+ Memory Versus Effector Development![]() ![]()
Following infection, naïve CD8+ T cells bearing pathogen-specific T cell receptors (TCRs) differentiate into a mixed population of short-lived effector and long-lived memory T cells to mediate an adaptive immune response. How the TCR regulates memory T cell development has remained elusive. Using a mutant TCR transgenic model, we found that point mutations in the TCR β transmembrane domain (βTMD) impair the development and function of CD8+ memory T cells without affecting primary effector T cell responses. Mutant T cells are deficient in polarizing the TCR and in organizing the nuclear factor
1 Experimental Transplantation Immunology, Department of Biomedicine, University Hospital-Basel, Hebelstrasse 20, 4031-Basel, Switzerland. B signal at the immunological synapse. Thus, effector and memory states of CD8+ T cells are separable fates, determined by differential TCR signaling.
2 Department of Molecular Microbiology and Immunology, University of Missouri, School of Medicine, Center for Cellular and Molecular Immunology, Columbia, MO 65212, USA. 3 Center for Immunology and Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis, MN 55454, USA. 4 Department of Immunology, Fundación Jiménez Díaz, Avenida Reyes Católicos 2, 28040-Madrid, Spain. 5 Department of Immunology, Mayo Clinic College of Medicine, Rochester, MN 55905,USA. * These authors have contributed equally to this work.
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Science. ISSN 0036-8075 (print), 1095-9203 (online)