Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1983 Jul;11(3):149-54.

Immunoregulatory mechanisms in pregnancy. II. Further characterization of suppressor lymphocytes induced by alpha-fetoprotein in lymphoid cell cultures

  • PMID: 6193275

Immunoregulatory mechanisms in pregnancy. II. Further characterization of suppressor lymphocytes induced by alpha-fetoprotein in lymphoid cell cultures

V Toder et al. J Clin Lab Immunol. 1983 Jul.

Abstract

Nonspecific suppressor cell (SPC) activity has been induced in vitro by preculturing splenocytes from normal mice in the presence of mouse amniotic fluid (MAF) and alpha-fetoprotein for 5 days or more. In adoptive transfer experiments in vivo, these AFP-precultured SPC were shown to reduce the humoral response of mice to sheep red blood cells and the cell-mediated cytotoxic response to allogeneic tumor cells. In mixing experiments in vitro, using freshly explanted splenocytes, the AFP-precultured splenocytes abrogated the generation of specific cytotoxic T-lymphocytes in primary mixed lymphocyte-tumor cell cultures. Supernatants of such precultured cells had at best only a marginal effect. These suppressor cells were found to be nylon-wool nonadherent and their effect could be almost completely abolished by treatment with anti-Thy-1, 2 serum plus complement. SPC precursors were found to be sensitive to cyclophosphamide (in vivo) and to hydrocortisone (in vivo and in vitro). At the same time, they are resistant to different doses of radiation.

PubMed Disclaimer

MeSH terms

LinkOut - more resources