PERSISTENT EXPANSION, IN A HUMAN IMMUNODEFICIENCY VIRUS-INFECTED PERSON, OF V-BETA-RESTRICTED CD4(-LYMPHOCYTES THAT EXPRESS CYTOTOXICITY-ASSOCIATED MOLECULES AND ARE COMMITTED TO PRODUCE INTERFERON-GAMMA AND TUMOR-NECROSIS-FACTOR-ALPHA()CD8(+) T)
L. Weiss et al., PERSISTENT EXPANSION, IN A HUMAN IMMUNODEFICIENCY VIRUS-INFECTED PERSON, OF V-BETA-RESTRICTED CD4(-LYMPHOCYTES THAT EXPRESS CYTOTOXICITY-ASSOCIATED MOLECULES AND ARE COMMITTED TO PRODUCE INTERFERON-GAMMA AND TUMOR-NECROSIS-FACTOR-ALPHA()CD8(+) T), The Journal of infectious diseases, 178(4), 1998, pp. 1158-1162
The present study describes the persistent expansion of a subpopulatio
n of circulating double-positive CD4(+)CD8(+) T cells in a human immun
odeficiency virus(HIV)-infected person over 8 years, The percentage of
double-positive cells was remarkably stable with time and was not rel
ated to HIV plasma virus load. CD4(+)CD8(+) cells exhibited phenotypic
characteristics of activated memory T lymphocytes. Analysis of V beta
usage by the T cell receptors of these cells indicated restricted exp
ression to the V beta 14 and V beta 17 families, Most CD4(+)CD8(+) cel
ls constitutively expressed cytotoxicity-associated molecules (C1.7 an
d perforin) and were selectively committed to produce interferon-gamma
and tumor necrosis factor-alpha, cytokines involved in cytotoxic func
tion. The kinetics of changes in the relative proportion of single-pos
itive CD4(+) and double-positive CD4(+)CD8(+) T cell subsets and a sim
ilar bias in V beta usage by these subsets suggest that CD4(+)CD8(+) l
ymphocytes originate from peripheral expansion of mature CD4(+) T cell
s.