TY - JOUR
T1 - Kinetics of human T-cell expression of LFA-1, IL-2 receptor, and ICAM-1 following antigenic stimulation in vitro
AU - Hviid, L
AU - Felsing, A
AU - Theander, T G
N1 - Keywords: Adult; Cells, Cultured; Humans; Intercellular Adhesion Molecule-1; Kinetics; Lymphocyte Activation; Lymphocyte Function-Associated Antigen-1; Receptors, Interleukin-2; T-Lymphocytes
PY - 1993
Y1 - 1993
N2 - Numerous studies have examined kinetics of T-cell functional responses following non-specific and antigen-specific stimulation in vitro. However, while reports of phenotypic T-cell changes after non-specific stimulation are abundant, only little information on phenotypic effects of antigen-specific stimulation is available. In the present study we have examined phenotypic T-cell changes after in vitro stimulation by the antigens purified derivative of tuberculin (PPD) and tetanus toxoid (TT). We show that the well-established differences in kinetics of mitogen- and antigen-induced T-cell proliferation in vitro is paralleled by differential kinetics in the expression of the T-cell adhesion and activation antigens leukocyte function-associated antigen 1 (LFA-1; CD11a/CD18), interleukin-2 receptor (IL-2R; CD25), and intercellular adhesion molecule 1 (ICAM-1; CD54). Furthermore, the changes in expression of all 3 surface antigens showed similar kinetics, and correlated with the magnitude of the lymphoproliferative response. By day 8 (PHA-stimulation) or day 12 (PPD or TT stimulation), the lymphoproliferative response was essentially completed, the expression of CD11a and CD54 had approached prestimulation levels, and CD25 expression was decreasing. This indicates that T-cell expression of all the 3 surface antigens examined is reversible. While this is in agreement with previous reports of the expression kinetics of IL-2R and ICAM-1, this is the first report indicating that the regulation of T-cell surface expression of LFA-1 is bidirectional. The results are discussed in relation to phenotypic characterization of memory T cells.
AB - Numerous studies have examined kinetics of T-cell functional responses following non-specific and antigen-specific stimulation in vitro. However, while reports of phenotypic T-cell changes after non-specific stimulation are abundant, only little information on phenotypic effects of antigen-specific stimulation is available. In the present study we have examined phenotypic T-cell changes after in vitro stimulation by the antigens purified derivative of tuberculin (PPD) and tetanus toxoid (TT). We show that the well-established differences in kinetics of mitogen- and antigen-induced T-cell proliferation in vitro is paralleled by differential kinetics in the expression of the T-cell adhesion and activation antigens leukocyte function-associated antigen 1 (LFA-1; CD11a/CD18), interleukin-2 receptor (IL-2R; CD25), and intercellular adhesion molecule 1 (ICAM-1; CD54). Furthermore, the changes in expression of all 3 surface antigens showed similar kinetics, and correlated with the magnitude of the lymphoproliferative response. By day 8 (PHA-stimulation) or day 12 (PPD or TT stimulation), the lymphoproliferative response was essentially completed, the expression of CD11a and CD54 had approached prestimulation levels, and CD25 expression was decreasing. This indicates that T-cell expression of all the 3 surface antigens examined is reversible. While this is in agreement with previous reports of the expression kinetics of IL-2R and ICAM-1, this is the first report indicating that the regulation of T-cell surface expression of LFA-1 is bidirectional. The results are discussed in relation to phenotypic characterization of memory T cells.
M3 - Journal article
C2 - 7707342
SN - 0141-2760
VL - 40
SP - 163
EP - 171
JO - Journal of Clinical & Laboratory Immunology
JF - Journal of Clinical & Laboratory Immunology
IS - 4
ER -