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 May;49(1):153-60.

Effects of cyclosporin A on the metabolism of unstimulated and mitogen-activated lymphocytes

Effects of cyclosporin A on the metabolism of unstimulated and mitogen-activated lymphocytes

J E Kay et al. Immunology. 1983 May.

Abstract

The immunosuppressive drug cyclosporin A (CS-A) reduces the magnitude of T-lymphocyte activation by all mitogenic lectins tested. However, in all cases a proportion of the activation observed is resistant even to very high concentrations of the drug. This proportion depends on the mitogen used, the responses to concanavalin A (Con A) and soybean agglutinin (SBA) being much more strongly inhibited than the responses to phytohaemagglutinin (PHA) or pokeweed mitogen (PWM). The differential effects of CS-A on lymphocyte activation by these mitogens could not be accounted for by the magnitude of the mitogenic response, the mitogen concentration used or the dependence of the responses on the presence of accessory cells, and they were maintained when several different procedures were used to assess the degree of activation. CS-A effectively inhibited inhibited lymphocyte activation. CS-A effectively inhibited lymphocyte activation only when added prior to, or very shortly after, the mitogen. Its ability to inhibit the response to PHA was lost more rapidly than that of Con A. The rate of protein synthesis by unstimulated lymphocytes was also affected by CS-A over the concentration range required to inhibit activation by mitogens. Although this effect was smaller than the inhibition of mitogen activation, it was highly significant and reproducible, and could not be accounted for by inhibition of spontaneous activation occurring in the unstimulated cultures.

PubMed Disclaimer

References

    1. Exp Cell Res. 1970 Dec;63(2):411-21 - PubMed
    1. Immunology. 1982 Sep;47(1):115-21 - PubMed
    1. Biochim Biophys Acta. 1971 Oct 14;247(2):322-34 - PubMed
    1. Biochim Biophys Acta. 1975 Jan 20;378(2):241-50 - PubMed
    1. J Immunol. 1976 Jan;116(1):131-9 - PubMed

Publication types

LinkOut - more resources