Rb. Moss et al., EFFECT OF IMMUNIZATION WITH AN INACTIVATED GP120-DEPLETED HIV-1 IMMUNOGEN ON BETA-CHEMOKINE AND CYTOKINE PRODUCTION IN SUBJECTS WITH HIV-1 INFECTION, Journal of acquired immune deficiency syndromes and human retrovirology, 14(4), 1997, pp. 343-350
Objective: To measure beta-chemokine and cytokine production in HIV-1-
infected subjects undergoing treatment with HIV-1 immunogen (REMUNE).
Design: Open label treatment study. Methods: beta-Chemokine and cytoki
ne production in peripheral blood mononuclear cell (PBMC) culture. Res
ults: Interferon-gamma production (p = 0.04) and lymphocyte proliferat
ion (p = 0.001) to HIV-1 antigen-stimulated PBMCs increased after immu
nization with the HIV-1 immunogen. A correlation was demonstrated afte
r immunization between HIV-1 antigen-stimulated lymphocyte proliferati
on and interferon-gamma levels (r = 0.53, p = 0.04). No significant ch
ange after immunization was seen for interleukin-4 production. A signi
ficant increase in mean levels of HIV-1 antigen-stimulated RANTES (i.e
., regulated upon, activation normal T-cell expressed and secreted), w
as evident 1 month after immunization (p = 0.002) and remained elevate
d 3 months after immunization. RANTES production was decreased in CD8-
depleted PBMC cultures. Mean serum HIV-1 RNA copy numbers and CD4 cell
counts remained stable after immunization (p >0.5). A correlation was
demonstrated between HIV-1 antigen-stimulated interferon-gamma and RA
NTES production (r = 0.54, p = 0.002). Conclusions: This report descri
bes an augmentation of beta-chemokines and T-Hl-type cytokines from PB
MCs after immunization with the HIV-1 immunogen.