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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 3 (1974), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Despite their limited ability to synthesize immunoglobulins (only IgA and not IgM or IgG) lymphocytes of human colostrum and human breast milk can be stimulated by Newcastle disease virus to produce interferon in the same amount as do blood lymphocytes. The maximum interferon production by milk lymphocytes was found on the 4th and the 5th day postpartum.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Infection 3 (1975), S. 111-114 
    ISSN: 1439-0973
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bei erwachsenen Freiwilligen wurden Immunisierungsversuche mit lebenden Zytomegalieviren, welche durch 125 Passagen ausschließlich auf WI-38 Zellen attenuiert worden waren (TOWNE 125 Stamm), durchgeführt. Orale/nasale Applikation induzierte keine Antikörperbildung. Fluoreszierende IgG-Antikörper konnten bei allen zehn sero-negativen Probanden, welche die attenuierten Zytomegalieviren in einer Dosis von 103 TCD50 intramuskulär erhielten, vier Wochen nach Immunisierung gefunden werden. Zum Auftreten von IgM-Antikörpern kam es bei sieben der zehn Sero-Negativen. Klinisch traten nur geringfügige Lokalreaktionen und eine relative Lymphozytose auf. Es konnte keine Virusausscheidung nachgewiesen werden. Verschiedene bis jetzt noch ungeklärte Fragen müssen zuerst durch weitere „Impfversuche“ an Freiwilligen geklärt werden, bevor an eine generelle Durchimpfung weiblicher Adoleszenten gegen Zytomegalie gedacht werden kann.
    Notes: Summary Trials with live cytomegalovirus (TOWNE 125 strain), which was attenuated by 125 passages exclusively on WI-38 cells, were done in adult volunteers. No virus take occured after oral/nasal application. When 103 TCD50 was given intramuscularly an IgG antibody response was detected at four weeks in all of ten volunteers tested by immunofluorescence; an IgM response was found in seven. Only mild local side-effects and relative lymphocytosis were observed. No virus excretion was found. Many questions remain to be answered by further trials before a cytomegalovirus vaccine can be given to adolescent girls.
    Type of Medium: Electronic Resource
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