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Open AccessJournal ArticleDOI

Interferon preparations enhance phagocytosis in vivo.

R M Donahoe, +1 more
- 01 Apr 1976 - 
- Vol. 13, Iss: 4, pp 1250-1257
TLDR
It was concluded that the complexity of the response of mice to an inducer makes analysis of the role of IF in the ensuing events difficult, but it is very likely that the in vivo effects observed here are to some degree mediated by IF.
Abstract
Previous studies have shown that interferon (IF) preparations enhance phagocytic activity in cultured mouse peritoneal macrophages. It is shown here that cell culture fluids containing large amounts of IF, which had been treated with acid and clarified of the inducer, Newcastle disease virus, enhanced phagocytic activity when injected into mice. Enhanced phagocytic activity also was observed after injection of Newcastle disease virus into mice, but the contribution of IF to this event was unclear. The kinetics of the phagocytic response to inducers in vivo were biphasic. Depression of phagocytosis occurred around 16 to 18 h after injection of Newcastle disease virus. The observed enhancement began about 12 h later and lasted for at least 60 h more. It was concluded that the complexity of the response of mice to an inducer makes analysis of the role of IF in the ensuing events difficult. However, because of documented phagocytosis-enhancing effects of IF in vitro, it is very likely that the in vivo effects observed here are to some degree mediated by IF. On this basis, the concept of the activity of IF as a lymphokine is potentially expanded.

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Citations
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Journal ArticleDOI

Anti-viral activity induced by culturing lymphocytes with tumor-derived or virus-transformed cells. Enhancement of human natural killer cell activity by interferon and antagonistic inhibition of susceptibility of target cells to lysis.

TL;DR: Cell separation experiments support the hypothesis that interferon enhances the activity of natural killer cells rather than generating a new population of effector cells, and might render the natural killer cell system an inducible selective defense mechanism against tumor and virus-infected cells.
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Plasminogen activation and regulation of pericellular proteolysis.

TL;DR: Research into the mechanism and function of plasminogen activation, and the role of fibrin in the regulation of activator secretion, are presented.
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Interferon: an inducer of macrophage activation by polyanions.

TL;DR: Purified mouse fibroblast interferon directly rendered resting macrophages tumoricidal and the physicochemical properties and species specificity of the stimulatory agent fall within the present definition of IF.
Book ChapterDOI

Interferons with special emphasis on the immune system

TL;DR: First described in 1957, interferon are induced animal proteins that inhibit a wide range of viruses by inducing an intracellular antiviral state; however, many interferons are species-specific in their antiviral activity.
Journal ArticleDOI

Mechanisms of activation of human natural killer cells against tumor and virus-infected cells.

TL;DR: A number of investigators have recently described specific cytotoxic effects of human lymphocytes against human target cells, but these studies have been hampered by the fact that lymphocytes from normal donors were at least as reactive as those from cancer patients.
References
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Journal ArticleDOI

Interferon-like virus-inhibitor induced in human leukocytes by phytohemagglutinin.

TL;DR: The physicochemical and biological properties of this virus-inhibitor are similar to those of interferon induced by Newcastle disease virus, except for an instability at pH 2 and 10 and at 56°C.
Journal ArticleDOI

Interferon inhibits DNA synthesis induced in mouse lymphocyte suspensions by phytohaemagglutinin or by allogeneic cells.

TL;DR: The inhibition by interferon of DNA synthesis induced in mouse spleen lymphocytes by the non-viral stimuli phytohaemagglutinin (PHA) and allogeneic lymphocytes is reported, suggesting that by acting on lymphocytes, interferons plays a role in the immunological response of the host.
Journal ArticleDOI

Priming: a nonantiviral function of interferon.

TL;DR: Several other picornaviruses that failed to induce interferon in L cells, human embryonic lung cells, or monkey kidney cells did induceInterferon when these cells had been primed by homologous interferons, and priming appears to be a function ofinterferon separable from its antiviral activity.
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