Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 32-44 |
| Number of pages | 13 |
| Journal | Natural Immunity and Cell Growth Regulation |
| Volume | 10 |
| Issue number | 1 |
| State | Published - 1991 |
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