Title of article :
CD8+ T cells responding to influenza infection reach and persist at higher numbers than CD4+ T cells independently of precursor frequency
Author/Authors :
Powell، نويسنده , , Timothy J. and Brown، نويسنده , , Deborah M. and Hollenbaugh، نويسنده , , Joseph A. and Charbonneau، نويسنده , , Tina and Kemp، نويسنده , , Roslyn A. and Swain، نويسنده , , Susan L. and Dutton، نويسنده , , Richard W.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Abstract :
The activation, localization, phenotypic changes, and function of CFSE-labeled naive influenza-specific CD8+ and CD4+ T cells following influenza infection were examined. Response of adoptively transferred CD8+ T cells was seen earliest in draining lymph node. Highly activated cells were found later in the lung, airways, and spleen, were cytolytic, and expressed IFN-γ upon restimulation. Similar amounts of division at early time points, but higher numbers of CD8+ T cells, were detected at 9 and 30 days postinfection after cotransfer of CD4+ and CD8+ T cells followed by infection. Transfer of much smaller numbers of CD4+ and CD8+ T cells led to more extensive expansion but the same difference in final number between the two cell types. These studies demonstrate how CD8+ and CD4+ T cells respond to influenza at early time points postinfection and the differential kinetics of antigen-specific CD4+ and CD8+ T cells.
Keywords :
cell surface molecules , Cellular proliferation , Cellular activation , T lymphocytes , virus infection
Journal title :
Clinical Immunology
Journal title :
Clinical Immunology