Ms. Malnati et al., INCREASED PLASMA-LEVELS OF THE C-C CHEMOKINE RANTES IN PATIENTS WITH PRIMARY HIV-1 INFECTION, Journal of biological regulators and homeostatic agents, 11(1-2), 1997, pp. 40-42
To investigate the role played by chemokines in the natural history of
human immunodeficiency virus (HIV) infection, we measured the plasma
levels of RANTES, MIP-1 alpha and MIP-1 beta in a cohort of patients w
ith primary HIV-1 infection (PHI) followed longitudinally. The cohort
included 17 patients with well-documented history of acute HIV syndrom
e within two months of the first observation. This mean plasma concent
ration of RANTES, but not that of MIP-1 alpha or MIP-1 beta, was signi
ficantly higher in patients with PHI (192.3 ng/ml) than in five HIV-se
ronegative controls (8.0 ng/ml) studied during the same time period. T
reatment of blood with a cocktail of drugs preventing platelet activat
ion, followed by high-speed centrifugation, reduced the levels of RANT
ES by approximately 2 logs both in patients and in controls, indicatin
g that the bulk of RANTES was released by platelets, which are known t
o store this chemokine in their alpha-granules, in the immediate after
math of blood drawing. No correlation was seen between the levels of R
ANTES and the number of HIV genome equivalents in plasma. These data s
uggest that large amounts of pre-formed RANTES are stored in platelets
and, possibly, in other blood cells during the early phases of HIV in
fection. The possible role of this HIV-suppressive chemokine in the co
ntrol of viral replication during PHI remains to be established.