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10.1111/j.1348-0421.1992.tb02110.x

http://scihub22266oqcxt.onion/10.1111/j.1348-0421.1992.tb02110.x
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suck abstract from ncbi


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pmid1282653      Microbiol+Immunol 1992 ; 36 (10): 1061-75
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  • Mechanisms of augmented resistance of cyclosporin A-treated mice to influenza virus infection by trehalose-6,6 -dimycolate #MMPMID1282653
  • Sazaki K; Yoshida I; Azuma M
  • Microbiol Immunol 1992[]; 36 (10): 1061-75 PMID1282653show ga
  • Cyclosporin A (CsA), which is an immunosuppressive drug of helper T lymphocytes, diminished a resistance of mice to influenza virus infection. Mice inoculated intravenously with trehalose-6,6'-dimycolate (TDM, a glycolipid component of the cell wall of Mycobacterium) in an oil-in-water emulsion (TDM emulsion) recovered the resistance to influenza virus infection impaired by CsA. Number of antibody-producing cells was markedly reduced in CsA- and/or TDM-treated mice. Interferon production in lung of TDM-treated mice was augmented; however, it was extremely reduced not only in CsA-treated mice, but also in CsA- and TDM-treated mice. Activities of natural killer cells of CsA- and/or TDM-treated mice were not different from that of control mice. Numbers of lymphocytes in lung of TDM-treated mice and CsA- and TDM-treated mice were more predominantly increased than that of control mice. Analysis of lung lymphocytes by flow cytometry revealed no difference between the populations of L3T4+ T lymphocytes and Lyt-2.2+ T lymphocytes in CsA- and/or TDM-treated mice and the populations in control mice. However, the population of gamma delta T cell receptor positive (gamma delta TCR+) lymphocytes increased markedly in lung of TDM-treated mice and also CsA- and TDM-treated mice. In vitro experiments showed that macrophage cultures treated with TDM emulsion released a mediator(s) which activates T lymphocytes, but not B lymphocytes. These and our earlier results suggest that the recovered anti-influenza virus resistance of CsA-treated mice by treatment with TDM emulsion was caused by elicitation of macrophages with TDM, then activation of T lymphocytes, especially gamma delta TCR+ lymphocytes.
  • |Animals[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |Antibody-Producing Cells/immunology[MESH]
  • |Cells, Cultured[MESH]
  • |Cord Factors/*pharmacology[MESH]
  • |Cyclosporine/*pharmacology[MESH]
  • |Female[MESH]
  • |Immunity, Innate/drug effects[MESH]
  • |Influenza A virus/immunology[MESH]
  • |Injections, Intravenous[MESH]
  • |Interferons/biosynthesis[MESH]
  • |Killer Cells, Natural/drug effects/immunology[MESH]
  • |Lung/drug effects/immunology[MESH]
  • |Lymphocyte Activation/drug effects[MESH]
  • |Lymphocyte Subsets/drug effects/immunology[MESH]
  • |Macrophages/drug effects/immunology[MESH]
  • |Mice[MESH]
  • |Mice, Inbred BALB C[MESH]


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