A high mucosal blocking score is associated with HIV protection

BACKGROUND:Early steps of HIV infection are mediated by the binding of the envelope to mucosal receptors as α4β7 and the C-type lectins DC-SIGN and langerin. Previously Env-specific B-cell responses have been reported in highly exposed seronegative individuals (HESN). METHOD:Here, we studied gp120-s...

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Veröffentlicht in:AIDS (London) 2019-03, Vol.33 (3), p.411-423
Hauptverfasser: Girard, Alexandre, Rallón, Norma, Benito, José M, Jospin, Fabienne, Rodriguez, Carmen, Chanut, Blandine, Benjelloun, Fahd, Del Romero, Jorge, Verrier, Bernard, Lucht, Frédéric, Pin, Jean-Jacques, Genin, Christian, Biasin, Mara, Clerici, Mario, Paul, Stéphane
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Sprache:eng
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Zusammenfassung:BACKGROUND:Early steps of HIV infection are mediated by the binding of the envelope to mucosal receptors as α4β7 and the C-type lectins DC-SIGN and langerin. Previously Env-specific B-cell responses have been reported in highly exposed seronegative individuals (HESN). METHOD:Here, we studied gp120-specific antibodies ability to block HIV interaction with α4β7, DC-SIGN and/or langerinin HESN. New cell-based assays were developed to analyze whether antibodies that can alter gp120 binding to α4β7, DC-SIGN and/or langerin are induced in HESN. A mucosal blocking score (MBS) was defined based on the ability of antibodies to interfere with gp120/α4β7, gp120/DC-SIGN, and gp120/langerin binding. A new MBS was evaluated in a cohort of 86 HESN individuals and compared with HIV patients or HIV unexposed healthy individuals. RESULTS:Antibodies reducing gp120 binding to both α4β7 and DC-SIGN were present in HESN serum but also in mucosal secretions, whereas antibodies from HIV patients facilitated gp120 binding to DC-SIGN. Any correlation was observed between MBS and the capacity of antibodies to neutralize infection of α4β7 CD4 T cells with primary isolates. CONCLUSIONS:MBS is significantly associated with protection in HESN and might reflect altered HIV spreading to mucosal-associated lymphoid tissues.
ISSN:0269-9370
1473-5571
DOI:10.1097/QAD.0000000000002099