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Department of Microbiology and Immunology, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157
Following intranasal administration, the model paramyxovirus simian
virus 5 (SV5) establishes an infection in the respiratory tract of
mice, which is subsequently cleared by CD8+ T cells. In
this study, we sought to understand the maturation of the antiviral
immune response over time by assessing the functional avidity of the
responding T cells and the expansion of immunodominant populations.
Surprisingly, we determined that the initial response to Ag at day 3
(d3) in the mediastinal lymph node was exclusively high avidity.
However, by d5 postinfection, low avidity cells were
50% of the
responding T cell population. Following secondary exposure to SV5, high
avidity CD8+ T cells again are the exclusive cell type
present at early times postinfection (d2). Similarly, high avidity
cells were preferentially elicited at d3 following infection with the
unrelated vaccinia virus. We also made the observation that the
immunodominance profile has not been established at d3 postinfection
with SV5. However, by d5 a clear immunodominance pattern arises and is
permanently maintained. These data indicate that high avidity cells are
the predominant population responding at early times postinfection
following respiratory infection with SV5 or vaccinia virus. However, as
the response progresses, low avidity cells are activated/expanded to a
greater extent compared with high avidity cells.
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