Expression of intracellular IFN-gamma in HSV-1-specific CD8(+) T cells identifies distinct responding subpopulations during the primary response to infection
H. Andersen et al., Expression of intracellular IFN-gamma in HSV-1-specific CD8(+) T cells identifies distinct responding subpopulations during the primary response to infection, J IMMUNOL, 165(4), 2000, pp. 2101-2107
Cutaneous infection in the footpads of C57BL/6 mice with HSV-1 results in a
n accumulation of activated (CD44(high) CD25(+)) CD8(+) T cells within the
draining popliteal lymph node (PLN), These studies were undertaken to evalu
ate the frequency and phenotype of the CD8(+) T cell population within the
PLN, recognizing the single immunodominant HSV-1 epitope derived from the v
iral envelope glycoprotein, glycoprotein B (gB), using an intracellular IFN
-gamma-staining assay. It revealed that similar to 6% of the CD8(+) T cells
were specific for the gB epitope, Phenotypic analysis of the IFN-gamma-pro
ducing gB-specific CD8(+) T cells generated in the PLN during the course of
the acute infection expressed the CD44(high) CD25(+) phenotype on days 3-5
postinfection. Surprisingly, IFN-gamma-producing CD8(+) T cells expressed
the CD44(high) CD25(-) phenotype on days 5-8 postinfection, in contrast to
expectations for a CD8(+) effector T cell. IFN-gamma-producing CD25(-) CD8(
+) T cells were detected in the PLN on day 21 postinfection, long after inf
ectious virus had been cleared. Throughout the response, the spleen was fou
nd to be the major reservoir of gB-specific CD8(+) T cells, even during the
peak of the response. In contrast to the gB-specific CD8(+) T cell populat
ion within the PLN, the entire gB-specific CD8(+) T cell population within
the spleen was CD25(-). Collectively, these results suggest the generation
of subpopulations of virus-specific CD8(+) T cells, distinguished by the ex
pression of CD25, during the acute phase of the primary response to a local
ized viral infection.