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Interleukin-12

Brunda, Michael J·1994·Journal of Leukocyte Biology

Abstract

Interleukin-12 (IL-12) is a newly characterized cytokine that has a unique heterodimeric structure. It was initially cloned from B lymphoblastoid cell lines, but the majority of IL-12 is produced by macrophages/monocytes following appropriate stimulation. IL-12 can (1) enhance the cytolytic activity of a number of effector cells including T cells, natural killer (NK) cells, lymphokine activated killer (LAK) cells, and macrophages, (2) increase proliferation of activated NK and T cells, (3) induce production of cytokines, such as interferon gamma, (4) stimulate the induction of ThI cells, (5) upregulate a number of cell surface molecules, (6) inhibit IgE secretion, and (7) act as a synergistic factor for hematopoietic stem cells. Based on these potent immunomodulatory activities, IL-12 has been evaluated in several disease models for parasitic infections and malignancies. Marked activity of IL-12 against both Lcishmania and Toxoplasma has been reported. Likewise, antimetastatic and antitumor activity, including tumor regression, has been observed against a number of murine malignancies treated with IL-12 using doses that result in little toxicity. The results suggest that IL-12 may be a useful cytokine for the treatment of a number of diseases. J. Leukoc. Biol. 55: 280–288; 1994.

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Metadata

Authors
Brunda, M. J.
Venue
Journal of Leukocyte Biology
Published
1994-02-01
Volume
55
Issue
2
Pages
280-288
ISSN
  • 0741-5400 (ISSN-L)
  • 1938-3673
OpenAlex
W4250647025
Cited by
295
References
0
FWCI
10.12
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Interleukin-12. https://app.cochat.ai/papers/10.1002/jlb.55.2.280
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Brunda, M. J. (1994). Interleukin-12. Journal of Leukocyte Biology. https://doi.org/10.1002/jlb.55.2.280

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