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Effect of sex hormones on human T cell activation by concanavalin A

  • I. Yron
  • , A. Langer
  • , T. Weinstein
  • , E. Sahar
  • , Y. Lidor
  • , Y. Pardo
  • , I. Katz
  • , L. Shohat
  • , Y. Kalechman
  • , J. Ovadia
  • , I. P. Witz
  • , B. Sredni
  • The Moise and Frida Eskenasy Institute for Cancer Research

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

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 languageEnglish
Pages (from-to)32-44
Number of pages13
JournalNatural Immunity and Cell Growth Regulation
Volume10
Issue number1
StatePublished - 1991
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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