RANTES PRODUCTION IN HIV-1 ANTIGEN-STIMULATED WHOLE-BLOOD CULTURE - RELATIONSHIP WITH TYPE-1 IMMUNE-RESPONSE AND PLASMA VIRAL LOAD IN INDIVIDUALS INFECTED WITH HIV-1
S. Benyoucef et al., RANTES PRODUCTION IN HIV-1 ANTIGEN-STIMULATED WHOLE-BLOOD CULTURE - RELATIONSHIP WITH TYPE-1 IMMUNE-RESPONSE AND PLASMA VIRAL LOAD IN INDIVIDUALS INFECTED WITH HIV-1, Scandinavian journal of immunology, 48(2), 1998, pp. 212-216
Host factors which control replication and clearance of human immunode
ficiency virus (HIV) are poorly understood. RANTES (regulated on activ
ation, normal T cell expressed and secreted) and other beta-chemokines
may be HIV-1-suppressive factors but their role in the progression of
HIV-1 infection is a subject of controversy. We investigated the rela
tionship between production of RANTES and correlates of disease progre
ssion in 15 patients infected with HIV-1. We used whole blood culture
to study the production of RANTES, interferon (IFN)-gamma, interleukin
(IL)-4 and IL-13 in response to supernatant of T cells infected with
HIV-1. A defect of RANTES production was associated with a predominant
type 2 and decreased type 1 cytokine profile (IL-4 and/or IL-13 > IFN
-gamma). We obtained a positive correlation between RANTES and IFN-gam
ma (P = 0.004) and the ratio of type 1 and type 2 cytokines IFN-y/IL-4
(P = 0.04) and IFN-gamma/IL-13 (P = 0.003), and a negative correlatio
n between RANTES production and HIV-1 RNA copy number in plasma (P = 0
.01). The same pattern of correlation was observed between HIV-1 p24-s
timulated production of RANTES and the plasma viral load (P = 0.02, n
= 15). The measurement of RANTES produced by heparinized whole blood i
n response to HIV-1 antigens appears as a potentially valuable tool to
assess the defect of type 1 immune response in individuals infected w
ith HIV-1 and to define whether the absence of a RANTES response may p
lay a role in the increased rate of HIV-1 replication.