Memory Thy-1(+)CD8(+) T cells specific for the
influenza A virus nucleoprotein (NP(366-374))
peptide were sorted after staining with the
D(b)NP(366) tetramer, labeled with
CFSE, and transferred into normal Thy-1.2(+) recipients. The donor
D(b)NP(366)(+) T cells recovered 2 days later from the spleens of the Thy-1.2(+) hosts showed the CD62L(low)CD44(high)CD69(low) phenotype, characteristic of the population analyzed before transfer, and were present at frequencies equivalent to those detected previously in mice primed once by a single exposure to an influenza A virus. Analysis of
CFSE-staining profiles established that resting tetramer(+) T cells divided slowly over the next 30 days, while the numbers in the spleen decreased about 3-fold. Intranasal
infection shortly after cell transfer with a noncross-reactive influenza B virus induced some of the donor
D(b)NP(366)(+) T cells to cycle, but there was no increase in the total number of transferred cells. By contrast, comparable challenge with an influenza A virus caused substantial clonal expansion, and loss of the
CFSE label. Unexpectedly, the recruitment of naive Thy-1.2(+)CD8(+)
D(b)NP(366)(+) host
D(b)NP(366)(+) T cells following
influenza A challenge was not obviously diminished by the presence of the memory Thy-1.1(+)CD8(+)
D(b)NP(366)(+) donor
D(b)NP(366)(+) set. Furthermore, the splenic response to an
epitope (D(b)PA(224)) derived from the
influenza acid polymerase (PA(224-233)) was significantly enhanced in the mice given the donor
D(b)NP(366)(+) memory population. These experiments indicate that an apparent recall response may be comprised of both naive and memory CD8(+) T cells.