Journal of immunology (Baltimore, Md. : 1950) · 2000
Intestinal intraepithelial lymphocytes exert potent protective cytotoxic activity during an acute virus infection.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Müller S, Bühler-Jungo M, Mueller C
Аннотация
After systemic infection of mice with 104 PFU of lymphocytic choriomeningitis virus (LCMV), infected cells are detected simultaneously in various organs, including spleen and intestinal mucosa. Most notably, virus-infected cells are also present among CD11c+ dendritic cells in the subepithelial area of the small intestinal mucosa. Some of these virus-infected cells are in close spatial association with intestinal intraepithelial lymphocytes (IEL). Therefore, we compared virus-specific cytotoxic activity of CD8 splenocytes with that of IEL subsets. While ex vivo isolated TCRalphabeta+CD8alphaalpha+ IEL exert only minimal virus-specific cytotoxicity, maximum specific killing mediated by TCRalphabeta+CD8alphabeta+ IEL on day 8 postinfection exceeds maximum cytotoxic activity observed with CD8 splenocytes when assessed in vitro. Maximum cytotoxic activity of IEL is preceded by peak perforin and granzyme B mRNA expression in IEL around day 6 postinfection, suggesting a recent activation in situ. The antivirus cytotoxicity of in vivo primed IEL is further demonstrated by the protection from virus production in the spleen of mice infected with LCMV 10 h before adoptive cell transfer. These data indicate a potent priming of LCMV-specific IEL in situ after systemic LCMV infection and suggest that cytotoxic IEL markedly contribute to the elimination of virus-infected cells in the intestinal mucosa.
Предметные рубрики MeSH
Acute DiseaseAnimalsCD8 AntigensCD8-Positive T-LymphocytesCells, CulturedCytotoxicity, ImmunologicDendritic CellsGranzymesIntestinal MucosaKineticsLymphocyte ActivationLymphocyte SubsetsLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMacrophagesMembrane GlycoproteinsMiceMice, Inbred C57BLPerforinPore Forming Cytotoxic ProteinsRNA, MessengerReceptors, Antigen, T-Cell, alpha-betaSerine EndopeptidasesSpleenUp-RegulationVirus Replication