During the last few years much attention has been paid to the chemokines. C
hemokine receptors are necessary to render a target permissive for infectio
n by the human immunodeficiency virus (HIV) and high concentrations of chem
okines have been shown to protect against the progression of HIV disease to
wards death. In the present study, we investigated the capability of strenu
ous exercise to induce elevated plasma concentrations of the chemokines int
erleukin (IL)-8, macrophage inflammatory protein (MIP)-1 alpha and MLP-1 be
ta Eight male athletes completed the Copenhagen Marathon 1997. Blood was sa
mpled before, immediately after the run and every 30 min during a 4 h recov
ery period. Plasma chemokine concentrations were measured using enzyme-link
ed immunosorbent assays. The IL-8, MIP-1 alpha and MTP-beta concentrations
all peaked 0.5 h after the run when they were 6.7-fold, 3.5-fold and 4.1-fo
ld increased, respectively. The elevated concentrations of chemokines in pl
asma after exercise could have implications for HEV-infected individuals; a
possibility that needs further investigation. infects target cells by inte
racting with the cell surface protein CD4 and additional molecules, termed
coreceptors, which have been identified as members of the chemokine recepto
r family (Feng et al. 1996). Con-comitant expression of CD4 and a chemokine
receptor is necessary to render a target eel susceptible to infection with
HIV. Chemokines can prevent binding of HIV to the chemokine receptor by co
mpetitive inhibition and it has been suggested that factors influencing the
plasma concentrations of chemokines may therefore have the potential to af
fect the progression of HIV disease (Zagury et al. 1998). We and others hav
e previously shown that exercise induces production of the cytokines involv
ed in inflammation, especially IL-6 and IL-1ra (Drenth et al. 1995; Nieman
1997; Ostrowski et al. 1998a, b, 1999). The present study investigated to w
hat extent strenuous exercise affects the plasma concentrations of the chem
okines interleukin (IL)-8, macrophage inflammatory protein (MIP)-1 alpha an
d MTP-1 beta.