H. Aladdin et al., Effects of G-CSF on telomere lengths in PBMCs from human immunodeficiency virus-infected patients: Results from a randomized, placebo-controlled trial, SC J IMMUN, 52(2), 2000, pp. 212-216
Telomeres are unique terminal chromosomal structures, the length of which h
as been shown to decrease with cell division in vitro and with increased ag
e in vivo for human somatic cells. In human immunodeficiency virus (HIV)-1
infection, decrease of telomere length is primarily found in CD8(+) T cells
, and not in CD4(+) T cells. In this double-blind placebo-controlled study,
we investigated the effect of granulocyte colony stimulating factor (G-CSF
) treatment combined with highly active antiretroviral therapy (HAART) on m
ean telomere length in peripheral blood mononuclear cells (PBMC). The termi
nal restriction fragment (TRF) length showed no changes during G-CSF treatm
ent although the number of lymphocytes increased significantly. The mean TR
F length correlated positively (R = 0.552, P = 0.009) and negatively (R = -
0.503, P = 0.02) to the proportion of CD4(+) memory and naive cells, respec
tively. Our data suggest that during G-CSF treatment lymphocytes are recrui
ted by a combination of central and peripheral proliferation.