TY - JOUR
T1 - Correction to
T2 - Picking up speed: cell cycle regulation during effector CD8+ T cell differentiation (Medical Microbiology and Immunology, (2023), 212, 3, (253-260), 10.1007/s00430-023-00768-7)
AU - Kretschmer, Lorenz
AU - Fuchs, Noémie
AU - Busch, Dirk H.
AU - Buchholz, Veit R.
N1 - Publisher Copyright:
© 2023, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2023/6
Y1 - 2023/6
N2 - There is a small error in presentation of Fig. 1. The correct figure (Fig. 1) is (Figure presented.) Competing models of memory T cell differentiation. A Plots depict the clonal expansion of antigen-specific CD8+ T cells in response to infection and their differentiation from naïve to effector to memory cells (Model I, left), as well as the predicted division histories of effector and memory subsets (right). B As in A, but showing the differentiation of naïve CD8+ T cells first into memory and then effector cells (Model II). C. Progressive model of CD8+ T cell differentiation, based on in vivo single cell fate mapping and population-derived data. Selected markers characterizing naïve, central memory precursor (CMP), effector memory precursor (EMP) and short-lived/terminal effector (SLEC/TE) cells are shown, as are the distinct functional properties of these subsets and a predicted increase of cell cycle speed upon transition from naïve to CMP, EMP and SLEC/TE cells The original article has been corrected.
AB - There is a small error in presentation of Fig. 1. The correct figure (Fig. 1) is (Figure presented.) Competing models of memory T cell differentiation. A Plots depict the clonal expansion of antigen-specific CD8+ T cells in response to infection and their differentiation from naïve to effector to memory cells (Model I, left), as well as the predicted division histories of effector and memory subsets (right). B As in A, but showing the differentiation of naïve CD8+ T cells first into memory and then effector cells (Model II). C. Progressive model of CD8+ T cell differentiation, based on in vivo single cell fate mapping and population-derived data. Selected markers characterizing naïve, central memory precursor (CMP), effector memory precursor (EMP) and short-lived/terminal effector (SLEC/TE) cells are shown, as are the distinct functional properties of these subsets and a predicted increase of cell cycle speed upon transition from naïve to CMP, EMP and SLEC/TE cells The original article has been corrected.
UR - http://www.scopus.com/inward/record.url?scp=85162221175&partnerID=8YFLogxK
U2 - 10.1007/s00430-023-00772-x
DO - 10.1007/s00430-023-00772-x
M3 - Comment/debate
AN - SCOPUS:85162221175
SN - 0300-8584
VL - 212
SP - 261
EP - 262
JO - Medical Microbiology and Immunology
JF - Medical Microbiology and Immunology
IS - 3
ER -