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
. 1970 Apr;18(4):501-15.

Studies of allograft immunity in mice. I. Induction, development and in vitro assay of cellular immunity

Studies of allograft immunity in mice. I. Induction, development and in vitro assay of cellular immunity

K T Brunner et al. Immunology. 1970 Apr.

Abstract

Cellular immunity induced by tumour allografts in inbred mice was studied with the help of an in vitro assay system measuring the cytotoxic effect of sensitized lymphocytes on 51Cr-labelled target cells. It is shown that lymphoid cells from spleen, lymph nodes and blood of the allograft recipients reach a peak of cytotoxic activity on days 10–11 after immunization. Incubated with labelled target cells at a ratio of 100:1, the sensitized lymphocytes caused the specific release of up to 70 per cent of the radioactivity within 1 hour. A second population of target cells added to the same cell suspension was destroyed at a slightly accelerated rate, suggesting stimulation of the effector cells by the first interaction. The cytotoxic activity of circulating lymphocytes was found to reach a plateau between days 20 and 60 after immunization, while the activity of spleen cells dropped to low levels in the same time period. The specificity of target cell destruction by sensitized lymphocytes is demonstrated by the lack of lytic activity for syngeneic target cells, and by the selective destruction of target cells carrying a tumour specific antigen. Tumour cells, lymphocytes and embryonic fibroblasts of the donor strain are shown to differ considerably in their sensitivity to lysis by immune lymphocytes.

PubMed Disclaimer

References

    1. Cancer Res. 1966 Jul;26(7):1508-15 - PubMed
    1. J Immunol. 1966 Aug;97(2):239-47 - PubMed
    1. Immunology. 1966 Nov;11(5):499-506 - PubMed
    1. Immunology. 1967 Oct;13(4):395-403 - PubMed
    1. Immunology. 1968 Feb;14(2):181-96 - PubMed

Substances

LinkOut - more resources