Abstract
We previously reported that aged mice demonstrated a 12-week delay in virus clearance compared to young mice after infection with E55+ murine leukemia retrovirus (E55+MuLV). The current study demonstrates that both the levels of IL-2, IFN-γ, and IL-10 and the number of cells producing IL-2 and IFN-γ were lower at 2 and 4 weeks postinfection (p.i.) in aged compared to young mice after virus-specific stimulation of spleen cells in vitro. In both age groups, IL-2 and IL-10 were produced by CD4+ T and B cells, respectively. IFN-γ was produced mainly by CD4+ T cells at 2 weeks p.i. and by CD4+ and CD8+ T cells at 4 weeks p.i. in young, but primarily by CD8+ T cells, in aged mice. Therefore, delayed virus clearance is associated with age-related decreases in type 1 and type 2 cytokines and a shift in the primary source of at least one cytokine.
Original language | English (US) |
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Pages (from-to) | 8-19 |
Number of pages | 12 |
Journal | Virology |
Volume | 299 |
Issue number | 1 |
DOIs | |
State | Published - 2002 |
Keywords
- Aging
- B cell
- CD4 T cell
- CD8 T cells
- IFN-γ
- IL-10
- IL-2
- Retrovirus
ASJC Scopus subject areas
- Virology