Multidimensional profiling of human T cells reveals high CD38 expression, marking recent thymic emigrants and age-related naive T cell remodeling
Pavla Boháčová(Washington University in St. Louis), Marina Terekhova(Washington University in St. Louis), Petr Tsurinov(Paphos General Hospital), Riley Mullins, Kamila Husarcikova(Washington University in St. Louis), Irina Shchukina(Washington University in St. Louis), Alina Ulezko Antonova(Washington University in St. Louis), Barbora Echalar(Washington University in St. Louis), Jan Kössl(Washington University in St. Louis), Adam Saidu(Washington University in St. Louis), Thomas Francis, Chelsea Mannie(Washington University in St. Louis), Laura Arthur(Washington University in St. Louis), Stephen D. R. Harridge, Daniel Kreisel, Philip A. Mudd, Angela M. Taylor(University of Virginia), Coleen A. McNamara, Marina Cella(Washington University in St. Louis), Sidharth V. Puram, Theo van den Broek(University Medical Center Utrecht), Femke van Wijk(University Medical Center Utrecht), Pirooz Eghtesady(Washington University in St. Louis), Maxim N. Artyomov
Cited by 44Open Access
Abstract
cells. Identification of RTEs enables direct assessment of thymic health. Furthermore, resolving the dynamics of naive T cell remodeling yields insight into vaccination and infection responsiveness throughout aging.
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