TY - JOUR
T1 - Effect of sex hormones on human T cell activation by concanavalin A
AU - Yron, Ilana
AU - Langer, A.
AU - Weinstein, T.
AU - Sahar, E.
AU - Lidor, Y.
AU - Pardo, Y.
AU - Katz, I.
AU - Shohat, L.
AU - Kalechman, Y.
AU - Ovadia, J.
AU - Witz, Isaac
AU - Sredni, B.
PY - 1991
Y1 - 1991
N2 - The effect of sex hormones on concanavalin A (Con A)-activated human T cells was studied. We show that neither 17β-estradiol (E2) nor progesterone, in concentrations of up to 10-6 M, alters the proliferative response of peripheral-blood mononuclear cells (PBMC) of healthy postmenopausal women. Furthermore, the hormones had no effect on the composition of T cell populations and on the expression of activation markers. We extended our study to a unique T cell population that is characterized by the ability to form rosettes with human erythrocytes, following Con A activation (designated autorosette-forming cells; ARFC) and known to manifest suppressive activity. Indeed, the in vitro addition of E2 (neither progesterone nor testosterone) to Con A-stimulated PBMC brought about 2- to 4-fold increase in the frequency of ARFC. Tamoxifen, an antiestrogen drug, reduced the frequency of estrogen-stimulated ARFC to the original low level. Furthermore, the inhibitory effect of growth medium from ARFC cultures originally stimulated with Con A + E2 was found to be higher than that of ARFC cultures originally stimulated with Con A alone.
AB - The effect of sex hormones on concanavalin A (Con A)-activated human T cells was studied. We show that neither 17β-estradiol (E2) nor progesterone, in concentrations of up to 10-6 M, alters the proliferative response of peripheral-blood mononuclear cells (PBMC) of healthy postmenopausal women. Furthermore, the hormones had no effect on the composition of T cell populations and on the expression of activation markers. We extended our study to a unique T cell population that is characterized by the ability to form rosettes with human erythrocytes, following Con A activation (designated autorosette-forming cells; ARFC) and known to manifest suppressive activity. Indeed, the in vitro addition of E2 (neither progesterone nor testosterone) to Con A-stimulated PBMC brought about 2- to 4-fold increase in the frequency of ARFC. Tamoxifen, an antiestrogen drug, reduced the frequency of estrogen-stimulated ARFC to the original low level. Furthermore, the inhibitory effect of growth medium from ARFC cultures originally stimulated with Con A + E2 was found to be higher than that of ARFC cultures originally stimulated with Con A alone.
UR - http://www.scopus.com/inward/record.url?scp=0026087693&partnerID=8YFLogxK
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AN - SCOPUS:0026087693
SN - 0254-7600
VL - 10
SP - 32
EP - 44
JO - Natural Immunity and Cell Growth Regulation
JF - Natural Immunity and Cell Growth Regulation
IS - 1
ER -