CD14lowCD16high: A cytokine‐producing monocyte subset which expands during human immunodeficiency virus infection

N Thieblemont, L Weiss, HM Sadeghi… - European journal of …, 1995 - Wiley Online Library
N Thieblemont, L Weiss, HM Sadeghi, C Estcourt, N Haeffner‐Cavaillon
European journal of immunology, 1995Wiley Online Library
Infection with the human immunodeficiency virus HIV‐1 is associated with the expansion of
a CD14lowCD16high monocyte subset in peripheral blood. This subset, which represents a
minor subpopulation of monocytes in healthy individuals, increases during HIV infection
and, in patients with AIDS, may represent up to 40% of the total circulating monocyte cell
population. The CD14lowCD16high circulating monocytes co‐express MAX. 1, p150, 95
and HLADR which are typical of tissue macrophage markers. These cells also express …
Abstract
Infection with the human immunodeficiency virus HIV‐1 is associated with the expansion of a CD14lowCD16high monocyte subset in peripheral blood. This subset, which represents a minor subpopulation of monocytes in healthy individuals, increases during HIV infection and, in patients with AIDS, may represent up to 40% of the total circulating monocyte cell population. The CD14lowCD16high circulating monocytes co‐express MAX.1, p150,95 and HLADR which are typical of tissue macrophage markers. These cells also express higher levels of intracellular interleukin (IL)‐1α and tumor necrosis factor (TNF)‐α than the CD14highCD16low monocyte population from the same patients. The CD14lowCD16high cells also express low levels of CD35, CD11a and CD4 in common with normal monocytes. When cultured in vitro, monocytes from HIV‐seropositive individuals differentiated within a few hours into an elongated fibroblastoid shape characteristic of migratory cells. Our results suggest that the expansion of the CD14lowCD16high monocyte subset, which produce high amounts of TNF‐α and IL‐1α, may participate in the immune dysfunction observed during HIV infection.
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