Arch Immunol Ther Exp (Warsz)
March 1991
Interferon production by leukocytes of 28 bronchial asthma patients and 27 normal subjects was examined using whole blood technique. Interferon production in blood samples was induced by classical inducers and the obtained interferons were tested in A549 cells using EMC virus as challenge. Leukocytes from both atopic and infectious asthma patients showed decreased ability to interferon production in comparison to healthy donors.
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November 1989
Investigations were carried out on 62 patients with atopic and nonatopic asthma and 70 normal individuals. Leukocytes isolated according to the method of Mogensen and Cantell, were induced for interferon production with Newcastle virus, H strain for 24 h at 37 degrees C in a tube culture placed in rolling drum. Interferon was assayed in the culture of human fibroblasts (HAT).
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November 1989
Investigations were carried out on 28 patients with nonatopic bronchial asthma treated with glycocorticosteroids or antibiotics and on 15 patients with atopic bronchial asthma treated with Alavac S vaccine. Leukocytes isolated from these patients by the method of Mogensen and Cantell were induced with Newcastle disease virus for interferon production, IFN was tested in the culture of human fibroblasts (HAT). The production of leukocytic IFN in glycocorticosteroids- and antibiotics-treated patients was shown to increase.
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July 1989
The effect of four antihistamines (Intal, Zaditen, Tavegyl, Benzhydramine) on interferon production in mice was investigated. The agents were administered in vivo to ovalbumin-sensitized and non-sensitized mice, or in vitro to isolated peritoneal cell cultures. The cells were induced for interferon production with Newcastle virus.
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January 1987
The present study was undertaken to test the effect of sensitization of mice with ovalbumin on the course of influenza virus infection. It was shown that the endogenous interferon level as well as degree of degranulation of lung mast cells were higher in sensitized and influenza virus-infected mice than in infected and nonsensitized ones. Also, lung cells of mice subjected to influenza virus effect in vitro revealed higher degranulation degree.
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October 1984
Investigations were carried out on the effect of Vaccinum cholericum, Polyvaccinum and Alavac S preparations on interferon synthesis in mouse. These preparations, injected i.v.
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October 1984
The present paper discusses the correlation between NDV-induced interferon production and the degree of histamine release from mouse mastocytes. The injection of mice with Newcastle virus was observed to substantially increase the percentage of released histamine and the degree of mastocytes degranulation. A clear-cut correlation was observed between virus-induced interferon titer and the degree of histamine release both in nonsensitized (control) as well as in sensitized mice.
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June 1985
The effect of verapamil, calcium antagonist, on the IFN production, the histamine release and degranulation of mastocytes were studied. The mastocytes were harvested from mice sensitized with ovalbumin, treated with verapamil and induced with Newcastle virus (NDV) to the interferon production (IFN). It has been shown that the percentage of degranulation was lower in mastocytes of the mice treated with verapamil, both induced with NDV and non-induced ones.
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January 1984
The investigations carried out showed the dependence of immunosuppression induced by A/USRR/053/74(H3N2) virus upon the activity of its neuraminidase. High activity of this enzyme influenced interferon (IFN) induction which, in turn, reduced the primary humoral response to sheep red blood cells (SRBC) or stimulated the production of IgM and IgG antibody producing cells.
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November 1980
The investigation was carried on mice infected with influenza A/053/74/H3N2 virus. 129/Ao/Boy, inbred mice, were inoculated intranasally with influenza virus. The alveolar and peritoneal cells from infected and uninfected animals were induced in vitro with Newcastle disease virus.
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February 1980
Antigenic analysis of strains isolated in the USSR during the epidemic in 1974/1975 showed differences in the hemagglutination inhibition test and in neuramidase activity with antisera against three reference strains. Strains isolated in a later period of the epidemic were classified into subgroup A/Port Chalmers/1/73. Nearly all strains were effective inducers of interferon and were susceptible to this inhibitor of virus replication.
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June 1979
Production of interferon by the peritoneal and alveolar cells as well as the production of antibody-producing cells by spleen in the experimental influenza in the mouse has been studied. At the time when the replication of virus lung was at the peak the alveolar cells, but not peritoneal cells were found to produce in vitro more interferon than the cells from the uninfected mice. At the same time in the spleen increased number of antibody forming cells (PFC) against sheep red blood cells was observed.
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February 1978
The present study was undertaken to compare the production of interferon by immunized mice in response to different viral inducers. Porton mice were immunized with NDV or A/Wr11/57 virus by injecting 6-week-old animals with virus on days 1, 7, and 14. The interferon response was investigated 3 weeks later.
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January 1975
Arch Immunol Ther Exp (Warsz)
October 1969
Arch Immunol Ther Exp (Warsz)
December 1966
Arch Immunol Ther Exp (Warsz)
November 1998
Arch Immunol Ther Exp (Warsz)
November 1998