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
. 1964 Jul 1;120(1):105-20.
doi: 10.1084/jem.120.1.105.

THE IMMUNOLOGICAL BASIS OF ACQUIRED CELLULAR RESISTANCE

THE IMMUNOLOGICAL BASIS OF ACQUIRED CELLULAR RESISTANCE

G B MACKANESS. J Exp Med. .

Abstract

The resistance developed by mice during infection with Listeria monocytogenes, Brucella abortus, or Mycobacterium tuberculosis is not specifically directed against the infecting organism. The processes involved in the induction of acquired resistance, however, are highly specific and seem to depend upon two factors: a state of immunological reactivity of the host and the presence of the specific microbial antigens to which the host has become reactive. When these two coexist in the tissues the host is found to be non-specifically resistant. It is suggested that resistance, which was shown to depend upon an altered state of host macrophages, may be due to the interaction of antigen and a specific antibody adsorbed to the surface of host macrophages; and that the antibody involved in the reaction is perhaps identical with the antibody which confers the state of delayed-type hypersensitivity. The results are discussed in relation to the question of latent infection and infection immunity.

PubMed Disclaimer

References

    1. Br J Exp Pathol. 1963 Dec;44:608-11 - PubMed
    1. Experientia. 1950 Nov 15;6(11):410-9 - PubMed
    1. Am Rev Respir Dis. 1962 Mar;85:364-72 - PubMed
    1. J Exp Med. 1962 Sep 1;116:381-406 - PubMed
    1. Lancet. 1963 Dec 7;2(7319):1203-4 - PubMed