Evidence map›Paper›PMID 39702373›Full record

ArticleNPJ vaccines2024

SPA14 liposomes combining saponin with fully synthetic TLR4 agonist provide adjuvanticity to hCMV vaccine candidate.

Ernesto Luna, Sophie Ruiz, Marie Garinot, Cyril Chavagnac, Pankaj Agrawal, John Escobar, Laurent Revet, Marie-Jeanne Asensio, Fabienne Piras, Francis G Fang and 4 more

Erratum issuedAbstract read
In one paragraph

Article in NPJ vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Ernesto Luna *Sanofi Vaccines business unit, R&D, Orlando, FL, USA.
Sophie Ruiz *Sanofi Vaccines business unit, R&D, Marcy L'Etoile, France.ORCID http://orcid.org/0000-0002-1919-3100
Marie Garinot *Sanofi Vaccines business unit, R&D, Marcy L'Etoile, France.
Cyril ChavagnacSanofi Vaccines business unit, R&D, Marcy L'Etoile, France.ORCID http://orcid.org/0009-0001-2625-2842
Pankaj AgrawalSanofi Vaccines business unit, R&D, Orlando, FL, USA.
John EscobarSanofi Vaccines business unit, R&D, Orlando, FL, USA.
Laurent RevetSanofi Vaccines business unit, R&D, Marcy L'Etoile, France.
Marie-Jeanne AsensioSanofi Vaccines business unit, R&D, Marcy L'Etoile, France.
Fabienne PirasSanofi Vaccines business unit, R&D, Marcy L'Etoile, France.
Francis G FangEisai Inc, Cambridge, MA, USA.
Donald R DrakeSanofi Vaccines business unit, R&D, Orlando, FL, USA.
Bachra RokbiSanofi Vaccines business unit, R&D, Marcy L'Etoile, France.
Daniel LarocqueSanofi Vaccines business unit, R&D, Marcy L'Etoile, France.ORCID http://orcid.org/0000-0002-2514-3687
Jean HaenslerSanofi Vaccines business unit, R&D, Marcy L'Etoile, France. jean.haensler@sanofi.com.ORCID http://orcid.org/0000-0002-3471-973X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the aim of designing and developing a novel saponin-based adjuvant system, we combined the QS21 saponin with low microgram amounts of the fully synthetic TLR4 agonist, E6020, in cholesterol-containing liposomes. The resulting adjuvant system, termed SPA14, appeared as a long-term stable and homogeneous suspension of mostly unilamellar and a few multilamellar vesicles, with an average hydrodynamic diameter of 93 nm, when formulated in citrate buffer at pH 6.0-6.5. When compared in an in vitro human innate immunity construct to AS01B, the QS21/MPL® liposomal adjuvant system of GSK, and with QS21-Liposomes used as benchmarks, SPA14 displayed the strongest immunostimulatory potential based on antigen-presenting cell (APC) activation and cytokine secretion, which was essentially driven by the highly active E6020 agonist in this assay. When tested as an adjuvant in vivo with human cytomegalovirus glycoprotein B (gB) and pentamer complex (PC) as test antigens, SPA14 was generally well tolerated and as active as AS01B for the induction of long-lasting CMV-neutralizing antibodies in mice and non-human primates (NHPs). Both adjuvants promoted the induction of Th-1 responses based on IgG2c production in mice and IFN-γ production in mice and NHPs, but in mice, a higher level of Th-2 cytokines (IL-5) and higher IgG1 over IgG2c secreting cells ratios were obtained with SPA14 indicating that the adjuvant profile of SPA14 could be less Th-1 biased than that of AS01B. From a developability standpoint, SPA14 could be manufactured by a simple and scalable ethanol injection method, owing to the high solubility in ethanol of all its lipidic components, including E6020. Furthermore, E6020 is a single molecule, well-characterized fully synthetic TLR4 agonist constructed in eight synthetic steps from entirely crystalline starting materials and intermediates via an optimized high-yield synthetic route. Overall, our data suggest that SPA14 is a viable, easy-to-manufacture, potent novel adjuvant system that could be broadly applicable as a ready-to-mix adjuvant in the form of a long-term stable liquid formulation.

Identifiers

PMID39702373
PMCPMC11659416

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.