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PMID: 6403616 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Recombinant mouse gamma interferon induces the priming step in macrophage activation for tumor cell killing.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 130 ·No. 5 ·1983-05-00 ·Pages 2011-3

Pace JL, Russell SW, Torres BA, Johnson HM, Gray PW

Abstract

Mouse macrophages become activated to kill tumor cells by traversing a series of steps (1-3). The first of these does not cause the expression of cytolytic activity; instead, it primes macrophages to respond to a second signal(s) that then triggers the onset of killing (4-7). The mediator that is responsible for priming is contained, along with other lymphokines, in the culture supernatants of concanavalin A-stimulated spleen cells (5-7) cloned T lymphocytes (8), or some T cell hybridomas (9). Close association has been noted between macrophage priming activity and antiviral activity that is attributable to gamma interferon (10-12). However, unequivocal evidence that the two activities are products of the same molecule has not been available. We now how conclusively by using mouse gamma interferon (MulFN-gamma)3 produced by recombinant DNA technology that, in addition to antiviral activity, this lymphokine has the capacity to induce the priming step in the process of macrophage activation for tumor cell killing.

MeSH Terms
Animals Cytotoxicity, Immunologic Interferon-gamma/physiology Lipopolysaccharides/pharmacology Macrophage Activation Male Mast-Cell Sarcoma/immunology Mice Mice, Inbred C3H
Chemicals
Lipopolysaccharides Interferon-gamma
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Pace J L
Russell S W
Torres B A
Johnson H M
Gray P W
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1983-05-00
Pages
2011-3
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI 16428 · United States
NCI NIH HHS · CA 31199 · United States
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