author_facet Sakuma, T
Suenaga, T
Yoshida, I
Azuma, M
Sakuma, T
Suenaga, T
Yoshida, I
Azuma, M
author Sakuma, T
Suenaga, T
Yoshida, I
Azuma, M
spellingShingle Sakuma, T
Suenaga, T
Yoshida, I
Azuma, M
Infection and Immunity
Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
Infectious Diseases
Immunology
Microbiology
Parasitology
author_sort sakuma, t
spelling Sakuma, T Suenaga, T Yoshida, I Azuma, M 0019-9567 1098-5522 American Society for Microbiology Infectious Diseases Immunology Microbiology Parasitology http://dx.doi.org/10.1128/iai.42.2.567-573.1983 <jats:p>The mechanism of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection was investigated by determining the effect of splenectomy, antithymocyte serum, and antimacrophage serum on resistance. It was greatly reduced by these treatments, not only in normal mice, but also in mice treated with live or heat-inactivated BCG. Production of circulating interferon by ectromelia virus and Newcastle disease virus was augmented in BCG-treated mice and was markedly depressed by splenectomy and antithymocyte and antimacrophage serum treatments in both BCG-treated and normal mice. Carbon clearance activity was activated in BCG-treated mice, but splenectomy did not influence phagocytic activity. These results suggest that augmented interferon production in the spleens of BCG-treated mice plays a major role in enhanced resistance. Other possible mechanisms are discussed.</jats:p> Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection Infection and Immunity
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series Infection and Immunity
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title Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_unstemmed Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_full Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_fullStr Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_full_unstemmed Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_short Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_sort mechanisms of enhanced resistance of mycobacterium bovis bcg-treated mice to ectromelia virus infection
topic Infectious Diseases
Immunology
Microbiology
Parasitology
url http://dx.doi.org/10.1128/iai.42.2.567-573.1983
publishDate 1983
physical 567-573
description <jats:p>The mechanism of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection was investigated by determining the effect of splenectomy, antithymocyte serum, and antimacrophage serum on resistance. It was greatly reduced by these treatments, not only in normal mice, but also in mice treated with live or heat-inactivated BCG. Production of circulating interferon by ectromelia virus and Newcastle disease virus was augmented in BCG-treated mice and was markedly depressed by splenectomy and antithymocyte and antimacrophage serum treatments in both BCG-treated and normal mice. Carbon clearance activity was activated in BCG-treated mice, but splenectomy did not influence phagocytic activity. These results suggest that augmented interferon production in the spleens of BCG-treated mice plays a major role in enhanced resistance. Other possible mechanisms are discussed.</jats:p>
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author Sakuma, T, Suenaga, T, Yoshida, I, Azuma, M
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description <jats:p>The mechanism of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection was investigated by determining the effect of splenectomy, antithymocyte serum, and antimacrophage serum on resistance. It was greatly reduced by these treatments, not only in normal mice, but also in mice treated with live or heat-inactivated BCG. Production of circulating interferon by ectromelia virus and Newcastle disease virus was augmented in BCG-treated mice and was markedly depressed by splenectomy and antithymocyte and antimacrophage serum treatments in both BCG-treated and normal mice. Carbon clearance activity was activated in BCG-treated mice, but splenectomy did not influence phagocytic activity. These results suggest that augmented interferon production in the spleens of BCG-treated mice plays a major role in enhanced resistance. Other possible mechanisms are discussed.</jats:p>
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imprint American Society for Microbiology, 1983
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institution DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161, DE-Zi4, DE-Gla1, DE-15, DE-Pl11, DE-Rs1, DE-14, FID-BBI-DE-23, DE-105, DE-Ch1, DE-L229
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spelling Sakuma, T Suenaga, T Yoshida, I Azuma, M 0019-9567 1098-5522 American Society for Microbiology Infectious Diseases Immunology Microbiology Parasitology http://dx.doi.org/10.1128/iai.42.2.567-573.1983 <jats:p>The mechanism of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection was investigated by determining the effect of splenectomy, antithymocyte serum, and antimacrophage serum on resistance. It was greatly reduced by these treatments, not only in normal mice, but also in mice treated with live or heat-inactivated BCG. Production of circulating interferon by ectromelia virus and Newcastle disease virus was augmented in BCG-treated mice and was markedly depressed by splenectomy and antithymocyte and antimacrophage serum treatments in both BCG-treated and normal mice. Carbon clearance activity was activated in BCG-treated mice, but splenectomy did not influence phagocytic activity. These results suggest that augmented interferon production in the spleens of BCG-treated mice plays a major role in enhanced resistance. Other possible mechanisms are discussed.</jats:p> Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection Infection and Immunity
spellingShingle Sakuma, T, Suenaga, T, Yoshida, I, Azuma, M, Infection and Immunity, Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection, Infectious Diseases, Immunology, Microbiology, Parasitology
title Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_full Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_fullStr Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_full_unstemmed Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_short Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
title_sort mechanisms of enhanced resistance of mycobacterium bovis bcg-treated mice to ectromelia virus infection
title_unstemmed Mechanisms of enhanced resistance of Mycobacterium bovis BCG-treated mice to ectromelia virus infection
topic Infectious Diseases, Immunology, Microbiology, Parasitology
url http://dx.doi.org/10.1128/iai.42.2.567-573.1983