TY - JOUR
T1 - Kinetics of CCR7 expression differ between primary activation and effector memory states of TH1 and TH2 cells
AU - Calabresi, Peter A.
AU - Allie, Rameeza
AU - Mullen, Katherine M.
AU - Yun, Sung Hae
AU - Georgantas, Robert W.
AU - Whartenby, Katharine A.
N1 - Funding Information:
This work was supported by NIH RO1-NS41435.
PY - 2003/6
Y1 - 2003/6
N2 - We explored the kinetics of CCR7 expression on TH1 and TH2 polarized cells as well as on antigen-specific T cell lines at various stages of differentiation. A striking pattern of early (days 7-14) inducible CCR7 expression was seen preferentially on primary TH1 cell lines, as compared to TH2 cells, and was dependent on the strength and duration of the T cell receptor signal. Upon repeated restimulation (days 21-28) and differentiation, a switch occurred in which TH2 cells had high CCR7 expression, whereas TH1 cells lost CCR7 expression. Chronic (8 weeks and later) effector memory cell lines were 95% CCR7 negative. These data demonstrate an ordered pattern of CCR7 expression that suggest more rapid priming of TH1 cells in the lymph node, and delayed priming with prolonged CCR7 expression during TH2 responses, and may have implications for tracking TH1 effector T cells ex vivo in autoimmune diseases.
AB - We explored the kinetics of CCR7 expression on TH1 and TH2 polarized cells as well as on antigen-specific T cell lines at various stages of differentiation. A striking pattern of early (days 7-14) inducible CCR7 expression was seen preferentially on primary TH1 cell lines, as compared to TH2 cells, and was dependent on the strength and duration of the T cell receptor signal. Upon repeated restimulation (days 21-28) and differentiation, a switch occurred in which TH2 cells had high CCR7 expression, whereas TH1 cells lost CCR7 expression. Chronic (8 weeks and later) effector memory cell lines were 95% CCR7 negative. These data demonstrate an ordered pattern of CCR7 expression that suggest more rapid priming of TH1 cells in the lymph node, and delayed priming with prolonged CCR7 expression during TH2 responses, and may have implications for tracking TH1 effector T cells ex vivo in autoimmune diseases.
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U2 - 10.1016/S0165-5728(03)00127-9
DO - 10.1016/S0165-5728(03)00127-9
M3 - Article
C2 - 12799021
AN - SCOPUS:0038546732
SN - 0165-5728
VL - 139
SP - 58
EP - 65
JO - Journal of Neuroimmunology
JF - Journal of Neuroimmunology
IS - 1-2
ER -