EMD-43666
Triple tandem trimer immunogens for HIV-1 and influenza nucleic acid-based vaccines (H2/1 GCN4)
EMD-43666
Single-particle19.52 Å
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Map released: 17/04/2024
Last modified: 17/04/2024
Sample Organism:
Influenza A virus
Sample: Chimeric hemagglutinin in complex with CR9114 Fab.
Deposition Authors: Ferguson JA
,
Leon AN
,
Ward AB
Sample: Chimeric hemagglutinin in complex with CR9114 Fab.
Deposition Authors: Ferguson JA
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Triple tandem trimer immunogens for HIV-1 and influenza nucleic acid-based vaccines.
Del Moral-Sanchez I
,
Wee EG,
Xian Y,
Lee WH,
Allen JD
,
Torrents de la Pena A
,
Froes Rocha R,
Ferguson J,
Leon AN
,
Koekkoek S,
Schermer EE,
Burger JA,
Kumar S
,
Zwolsman R
,
Brinkkemper M,
Aartse A,
Eggink D,
Han J
,
Yuan M
,
Crispin M
,
Ozorowski G
,
Ward AB
,
Wilson IA
,
Hanke T
,
Sliepen K
,
Sanders RW
(2024) NPJ Vaccines , 9 , 74 - 74
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(2024) NPJ Vaccines , 9 , 74 - 74
Abstract:
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.
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.