Abstract
The placenta may play a critical role in inhibiting vertical transmission of HIV-1. Here we demonstrate that leukemia inhibitory factor (LIF) is a potent endogenous HIV-1-suppressive factor produced locally in placentae. In vitro, LIF exerted a potent, gp130-LIFRbeta-dependent, HIV coreceptor-independent inhibition of HIV-1 replication with IC50 values between 0.1 pg/ml and 0.7 pg/ml, depending on the HIV-1 isolate. LIF also inhibited HIV-1 in placenta and thymus tissues grown in ex vivo organ culture. The level of LIF mRNA and the incidence of LIF protein-expressing cells were significantly greater in placentae from HIV-1-infected women who did not transmit HIV-1 to their fetuses compared with women who transmitted the infection, but they were not significantly different from placentae of uninfected mothers. These findings demonstrate a novel pathway for endogenous HIV suppression that may prove to be an effective immune therapy for HIV infection.
Publication types
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Comment
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Cell Division / drug effects
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Cells, Cultured
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Contactins
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DNA, Viral / analysis
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Female
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Gene Expression
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Growth Inhibitors / pharmacology
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Growth Inhibitors / physiology*
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HIV Infections / transmission
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HIV-1 / drug effects
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HIV-1 / physiology*
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Humans
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In Vitro Techniques
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Interleukin-6*
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Leukemia Inhibitory Factor
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Leukemia Inhibitory Factor Receptor alpha Subunit
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Lymphokines / pharmacology
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Lymphokines / physiology*
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Monocytes / drug effects
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Neural Cell Adhesion Molecules / metabolism
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Placenta / immunology
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Placenta / metabolism*
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Placenta / virology
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RNA, Messenger / analysis
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Receptors, Cytokine / metabolism
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Receptors, OSM-LIF
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Reverse Transcriptase Polymerase Chain Reaction
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Up-Regulation
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Viral Load
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Virus Replication / drug effects
Substances
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Contactins
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DNA, Viral
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Growth Inhibitors
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Interleukin-6
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LIF protein, human
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LIFR protein, human
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Leukemia Inhibitory Factor
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Leukemia Inhibitory Factor Receptor alpha Subunit
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Lymphokines
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Neural Cell Adhesion Molecules
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RNA, Messenger
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Receptors, Cytokine
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Receptors, OSM-LIF