LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 2 of total 2

Search options

  1. Article: Cellular changes in lungs of mice infected with influenza virus: characterization of the cytotoxic responses.

    Wyde, P R / Cate, T R

    Infection and immunity

    1978  Volume 22, Issue 2, Page(s) 423–429

    Abstract: ... Nonspecific cytotoxicity for target cells infected with H3hkNeq1 or B/Lee influenza virus was found ... the cytotoxicity data suggest that the local T cell response to influenza virus infection in the lung is a major ... influenza A/Hong Kong/68 (H3N2) virus. Macrophages and lymphocytes in approximately equal numbers comprised ...

    Abstract Transpleural lavage of lungs from uninfected C3H mice yielded an average of 300,000 leukocytes per mouse. This number increased eightfold within 6 days after intranasal inoculation with virulent influenza A/Hong Kong/68 (H3N2) virus. Macrophages and lymphocytes in approximately equal numbers comprised 90% or more of the leukocytes both before and during infection. B, T, and null lymphocytes comprised, respectively, 9, 21, and 18% of the leukocytes before infection and 7, 26, and 5% by day 6. In absolute numbers, macrophages and T lymphocytes provided the major increments during infection. Cytotoxic activity of mononuclear cells from lung lavages was compared in a chromium release assay using syngeneic L929 target cells with the activity of mediastinal lymph nodes, spleens, and peripheral blood of uninfected and infected C3H mice. Nonspecific cytotoxicity for target cells infected with H3hkNeq1 or B/Lee influenza virus was found with mononuclear cells from uninfected mice. This activity tended to be highest with lavage leukocytes and was associated with adherent cells, presumably macrophages. Increased virus-specific cytotoxicity was detected with lavage cells by day 6 and persisted through day 9, the period of maximal pneumonia. Similar cytotoxic activity also appeared in cells from the nodes and spleen at this same time but was not detected in peripheral blood cells. The virus-specific cytotoxicity of lavage cells was due largely to a nonadherent cell possessing Fc receptors and theta antigen but lacking C3 receptors; these properties are compatible with actively cytotoxic T lymphocytes. The cytological characteristics of the infiltrating leukocytes and the cytotoxicity data suggest that the local T cell response to influenza virus infection in the lung is a major contributor to the pneumonia observed in this mouse model.
    MeSH term(s) Animals ; Cytotoxicity, Immunologic ; Lung/immunology ; Macrophages/immunology ; Male ; Mice ; Mice, Inbred C3H ; Orthomyxoviridae Infections/immunology ; Pneumonia, Viral/immunology ; T-Lymphocytes/immunology
    Language English
    Publishing date 1978-11
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 218698-6
    ISSN 1098-5522 ; 0019-9567
    ISSN (online) 1098-5522
    ISSN 0019-9567
    DOI 10.1128/iai.22.2.423-429.1978
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: The use of a TLR2 agonist-based adjuvant for enhancing effector and memory CD8 T-cell responses.

    Chua, Brendon Y / Olson, Matthew R / Bedoui, Sammy / Sekiya, Toshiki / Wong, Chinn Y / Turner, Stephen J / Jackson, David C

    Immunology and cell biology

    2014  Volume 92, Issue 4, Page(s) 377–383

    Abstract: ... complete Freund's adjuvant). The phenotypic changes observed in these mice vaccinated using R4Pam2Cys ... of pulmonary viral titres following challenge with a chimeric influenza virus containing the K(b)OVA257-264 ... a phenotype associated with strong recall responses against respiratory infections, are also increased ...

    Abstract We have previously shown that the immunogenicity of protein antigens can be significantly enhanced if electrostatically associated with the Toll-like receptor-2 agonist-based lipopeptide R4Pam2Cys. The precise mechanisms and effectiveness of the cytotoxic T-lymphocyte (CTL)-mediated response facilitated by this agonist, however, have not been studied. Here we show that priming by dendritic cells (DCs) in the draining lymph nodes of animals vaccinated with antigen delivered using R4Pam2Cys results in significantly improved T-cell proliferation and induces their differentiation into polyfunctional effector CTLs characterised by granzyme B expression and the ability to secrete interferon-γ, interleukin-2 and tumor necrosis factor-α 7 days after vaccination. After 30 days, frequencies of antigen-specific CD62(low)CD127(high) (effector memory), CD62(high)CD127(high) (central memory) and CD43(low)CD27(high) CD8(+) T cells, a phenotype associated with strong recall responses against respiratory infections, are also increased compared with responses obtained with antigens formulated in the adjuvants Alum (alhydrogel) and CFA (complete Freund's adjuvant). The phenotypic changes observed in these mice vaccinated using R4Pam2Cys further correlated with their ability to recall specific T cells into the lung to mediate the reduction of pulmonary viral titres following challenge with a chimeric influenza virus containing the K(b)OVA257-264 epitope compared with animals vaccinated using Alum or CFA. The findings from this study not only demonstrate that better T-cell responses can be elicited using R4Pam2Cys compared with classically utilised adjuvants but also highlight the potential effectiveness of this lipopeptide-based adjuvant particularly against viral infections that require resolution through cell-mediated immunity.
    MeSH term(s) Adjuvants, Immunologic/pharmacology ; Animals ; Antigen Presentation/drug effects ; CD8-Positive T-Lymphocytes/drug effects ; CD8-Positive T-Lymphocytes/immunology ; Cell Differentiation/drug effects ; Cell Differentiation/immunology ; Cell Proliferation/drug effects ; Immunologic Memory/drug effects ; Lipopeptides/pharmacology ; Mice, Inbred C57BL ; Ovalbumin/immunology ; Toll-Like Receptor 2/agonists ; Toll-Like Receptor 2/metabolism ; Vaccination
    Chemical Substances Adjuvants, Immunologic ; Lipopeptides ; S-(2,3-bis(palmitoyloxy)propyl)cysteine ; Toll-Like Receptor 2 ; Ovalbumin (9006-59-1)
    Language English
    Publishing date 2014-01-07
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 284057-1
    ISSN 1440-1711 ; 0818-9641
    ISSN (online) 1440-1711
    ISSN 0818-9641
    DOI 10.1038/icb.2013.102
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top