MODULATION OF HIV-1 REPLICATION BY CYTOKINES AND SOLUBLE CYTOKINE RECEPTORS

点击翻译按钮获取中文摘要

Macrophages (MO) are the first cells infected with HIV-1 in vivo and act as a reservoir for the virus. Cytokines are potent modulators of HIV, both enhancing and inhibiting virus replication. Since NK cells are the first line of defense against virus-infected cells and produce a number of cytokines which are biologically active on MO, we investigated the potential of NK cells to produce cytokines capable of preventing replication of HIV in MO. We found that purified NK cells treated with IL-2 and the NK cell lines, NK3.3 and YT, are rich sources of chemokines, including those which inhibit binding to the CCR-3 and CCR-5 chemokine co-receptors for HIV and those with monocyte and T cell chemotactic/ activating properties. Thus, NK cells produce multiple chemotactic factors capable of signalling through a wide variety of chemokine receptors. We also found that NK cells produce high levels of IL-10 as well as IL-13, a cytokine with potent monocyte differentiating properties and HIV inhibitory activity, but do not produce IL-4. Finally, we found that NK cells produce a novel factor which prevents HIV-1 replication following entry in MO, but not T cells. Partial purification indicates that the inhibitory factor(s) is a small molecule of approximately 10 kD with a pI between 8.0 and 10.0. The small size and basic pI are characteristic of a chemokine, but the ability of this factor to inhibit replication of HIV, and not merely virus entry, indicate that the factor is not a chemokine binding to CCR-5. Consistent with this are our findings that antibodies to the beta chemokines, including MIP-1 alpha, MIP-1 beta and RANTES, are unable to reverse the HIV-1-inhibitory effect when the NK cell-derived factor is added post infection to MO. In contrast, these antibodies can reverse the inhibitory effects observed when this factor is added during virus adsorption. Pertusis toxin, a potent inhibitor of G-protein coupled receptor activity, had no effect on the inhibitory activity. Taken together, our data suggest that the novel NK cell factor is distinct from beta chemokines known to inhibit HIV entry and that NK cells may play a greater role than anticipated in the regulation of HIV-1 expression in human MO. It is important to identify the cytokines involved and delineate their potential to inhibit HIV replication in vitro and in vivo. Interferon-alpha (IFN-a) has potent anti-retroviral activity in acute and chronic HIV-1 infection systems in vitro and its clinical utility has been shown in AIDS patients having high numbers of CD4+ T cells. However, IFN-a species vary in their ability to inhibit HIV replication in vitro, which may correlate with varying effects in vivo. Current studies will determine whether: 1) IFN-a components or recombinant hybrid species vary in their ability to inhibit acute HIV-1 infections of MO and T cells; 2) anti-HIV activity is associated with expression of inducible nitric oxide synthase; 3) anti-HIV activity correlates with anti-proliferative activity; and 4) whether a species of IFN-a with low anti-proliferative activity and high anti-HIV activity can be identified, which may cause fewer toxic side effects when used clinically.