Soluble HIV-1 envelope immunogens derived from an elite neutralizer elicit cross-reactive V1V2 antibodies and low potency neutralizing antibodies

• Published in: PloS one 2014-01, Vol.9 (1), p.e86905-e86905
• Main Authors: Carbonetti, Sara, Oliver, Brian G, Glenn, Jolene, Stamatatos, Leonidas, Sather, D Noah
• Format: Article
• Language: English
• Subjects: Acquired immune deficiency syndrome; AIDS; AIDS vaccines; Amino acids; Animals; Antibodies; Antibodies, Neutralizing - immunology; Biology; Cross Reactions; env Gene Products, Human Immunodeficiency Virus - immunology; Enzyme-Linked Immunosorbent Assay; Health risks; HIV; HIV Antibodies - immunology; HIV Infections - immunology; HIV Infections - virology; HIV-1 - immunology; Human immunodeficiency virus; Humans; Immunization; Medicine; Monomers; Neutralization Tests; Neutralizing; Proteins; Rabbits; Risk reduction; Trimers; Vaccination; Vaccines; Viral envelope proteins; Viruses
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0086905

We evaluated four gp140 Envelope protein vaccine immunogens that were derived from an elite neutralizer, subject VC10042, whose plasma was able to potently neutralize a wide array of genetically distinct HIV-1 isolates. We sought to determine whether soluble Envelope proteins derived from the viruses circulating in VC10042 could be used as immunogens to elicit similar neutralizing antibody responses by vaccination. Each gp140 was tested in its trimeric and monomeric forms, and we evaluated two gp140 trimer vaccine regimens in which adjuvant was supplied at all four immunizations or at only the first two immunizations. Interestingly, all four Envelope immunogens elicited high titers of cross-reactive antibodies that recognize the variable regions V1V2 and are potentially similar to antibodies linked with a reduced risk of HIV-1 acquisition in the RV144 vaccine trial. Two of the four immunogens elicited neutralizing antibody responses that neutralized a wide array of HIV-1 isolates from across genetic clades, but those responses were of very low potency. There were no significant differences in the responses elicited by trimers or monomers, nor was there a significant difference between the two adjuvant regimens. Our study identified two promising Envelope immunogens that elicited anti-V1V2 antibodies and broad, but low potency, neutralizing antibody responses.