Interplay of diverse adjuvants and nanoparticle presentation of native-like HIV-1 envelope trimers

Author:

Sliepen KwintenORCID,Schermer Edith,Bontjer IljaORCID,Burger Judith A.,Lévai Réka Felfödiné,Mundsperger PhilippORCID,Brouwer Philip J. M.,Tolazzi Monica,Farsang Attila,Katinger DietmarORCID,Moore John P.,Scarlatti GabriellaORCID,Shattock Robin J.ORCID,Sattentau Quentin J.ORCID,Sanders Rogier W.ORCID

Abstract

AbstractThe immunogenicity of HIV-1 envelope (Env) trimers is generally poor. We used the clinically relevant ConM SOSIP trimer to compare the ability of different adjuvants (squalene emulsion, ISCOMATRIX, GLA-LSQ, and MPLA liposomes) to support neutralizing antibody (NAb) responses in rabbits. The trimers were administered as free proteins or on nanoparticles. The rank order for the adjuvants was ISCOMATRIX > SE > GLA-LSQ ~ MPLA liposomes > no adjuvant. Stronger NAb responses were elicited when the ConM SOSIP trimers were presented on ferritin nanoparticles. We also found that the GLA-LSQ adjuvant induced an unexpectedly strong antibody response to the ferritin core of the nanoparticles. This “off-target” effect may have compromised its ability to induce the more desired antitrimer antibodies. In summary, both adjuvants and nanoparticle display can improve the magnitude of the antibody response to SOSIP trimers but the best combination of trimer presentation and adjuvant can only be identified experimentally.

Funder

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

Bill and Melinda Gates Foundation

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

EC | Horizon 2020 Framework Programme

U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Infectious Diseases,Pharmacology,Immunology

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