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Blood, 1 June 2006, Vol. 107, No. 11, pp. 4466-4474.
Prepublished online as a Blood First Edition Paper on February 9, 2006; DOI 10.1182/blood-2005-08-3490.
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IMMUNOBIOLOGY
Efficient inhibition of HIV-1 replication in human immature monocyte-derived dendritic cells by purified antiHIV-1 IgG without induction of maturation
Vincent Holl,
Maryse Peressin,
Sylvie Schmidt,
Thomas Decoville,
Susan Zolla-Pazner,
Anne-Marie Aubertin, and
Christiane Moog
From the Institut de Virologie, Strasbourg, France; and Veterans Affairs and New York University Medical Centers, NY.
During mucosal HIV transmission, immature dendritic cells (DCs) present in the mucosa are among the first cellular targets of the virus. Previous studies have analyzed the inhibition of HIV-1 transfer from human mature DCs to T lymphocytes by neutralizing IgG, but so far no in vitro data regarding the capacity of antibodies to inhibit HIV-1 infection of immature DCs have been reported. Here, we found an increased HIV-inhibitory activity of monoclonal IgG and purified polyclonal IgG when immature monocyte-derived dendritic cells (iMDDCs) were used as target cells instead of autologous blood lymphocytes. We showed that Fc RII is involved in the mechanism for inhibiting HIV-1 infection of iMDDCs by IgG, whereas no induction of maturation was detected at concentrations of IgG that result in a 90% reduction of HIV replication. After induction of Fc RI expression on iMDDCs by IFN- , an augmentation of the HIV-inhibitory activity of IgG, related to the expression of Fc RI, was observed. Taken together, our results demonstrate the participation of Fc Rs in HIV-1 inhibition by IgG when iMDDCs are the targets. We propose that IgG is able to efficiently inhibit HIV-1 replication in iMDDCs and should be one of the components to be induced by vaccination.

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