Triple tandem trimer immunogens for HIV-1 and influenza nucleic acid-based vaccines.
Iván Del Moral SánchezEdmund G WeeYuejiao XianWen-Hsin LeeJoel D AllenAlba Torrents de la PeñaRebeca Fróes RochaJames FergusonAndré Nicolás LeónSylvie KoekkoekEdith E SchermerJudith A BurgerSanjeev KumarRobby ZwolsmanMitch BrinkkemperAafke AartseDirk EgginkJulianna HanMeng YuanMax CrispinGabriel OzorowskiAndrew B WardIan A WilsonTomáš HankeKwinten SliepenRogier W SandersPublished in: NPJ vaccines (2024)
Recombinant native-like HIV-1 envelope glycoprotein (Env) trimers are used in candidate vaccines aimed at inducing broadly neutralizing antibodies. While state-of-the-art SOSIP or single-chain Env designs can be expressed as native-like trimers, undesired monomers, dimers and malformed trimers that elicit non-neutralizing antibodies are also formed, implying that these designs could benefit from further modifications for gene-based vaccination approaches. Here, we describe the triple tandem trimer (TTT) design, in which three Env protomers are genetically linked in a single open reading frame and express as native-like trimers. Viral vectored Env TTT induced similar neutralization titers but with a higher proportion of trimer-specific responses. The TTT design was also applied to generate influenza hemagglutinin (HA) trimers without the need for trimerization domains. Additionally, we used TTT to generate well-folded chimeric Env and HA trimers that harbor protomers from three different strains. In summary, the TTT design is a useful platform for the design of HIV-1 Env and influenza HA immunogens for a multitude of vaccination strategies.
Keyphrases
- antiretroviral therapy
- hiv positive
- hiv infected
- hiv testing
- human immunodeficiency virus
- hepatitis c virus
- hiv aids
- nucleic acid
- men who have sex with men
- sars cov
- minimally invasive
- south africa
- dengue virus
- high throughput
- dna methylation
- working memory
- mesenchymal stem cells
- zika virus
- transcription factor
- drug induced