A systemically administered detoxified TLR4 agonist displays potent antitumor activity and an acceptable tolerance profile in preclinical models.

adjuvant effect in vivo antitumor activity lipopolysaccharides liposomal formulation modified TLR4 agonist tolerance

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 08 11 2022
accepted: 19 04 2023
medline: 26 5 2023
pubmed: 24 5 2023
entrez: 24 5 2023
Statut: epublish

Résumé

Bacterial lipopolysaccharides (LPS) are potent innate immunostimulants targeting the Toll-like receptor 4 (TLR4), an attractive and validated target for immunostimulation in cancer therapy. Although LPS possess anti-tumor activity, toxicity issues prevent their systemic administration at effective doses in humans. We first demonstrated that LPS formulated in liposomes preserved a potent antitumor activity

Identifiants

pubmed: 37223101
doi: 10.3389/fimmu.2023.1066402
pmc: PMC10200957
doi:

Substances chimiques

Adjuvants, Immunologic 0
Cytokines 0
Lipopolysaccharides 0
Liposomes 0
TLR4 protein, human 0
Tlr4 protein, mouse 0
Toll-Like Receptor 4 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1066402

Informations de copyright

Copyright © 2023 Chettab, Fitzsimmons, Novikov, Denis, Phelip, Mathé, Choffour, Beaumel, Fourmaux, Norca, Kryza, Evesque, Jordheim, Perrial, Matera, Caroff, Kerzerho and Dumontet.

Déclaration de conflit d'intérêts

KC, AN, JK, and MC are shareholders in HEPHAISTOS-Pharma. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Kamel Chettab (K)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.
Hospices Civils de Lyon, Lyon, France.

Chantel Fitzsimmons (C)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.

Alexey Novikov (A)

HEPHAISTOS-Pharma, Université Paris-Saclay, Orsay, France.

Morgane Denis (M)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.
Antinéo, Lyon, France.

Capucine Phelip (C)

HEPHAISTOS-Pharma, Université Paris-Saclay, Orsay, France.

Doriane Mathé (D)

Antinéo, Lyon, France.

Pierre Antoine Choffour (PA)

Antinéo, Lyon, France.

Sabine Beaumel (S)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.

Eric Fourmaux (E)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.

Patrick Norca (P)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.

David Kryza (D)

Hospices Civils de Lyon, Lyon, France.

Anne Evesque (A)

Antinéo, Lyon, France.

Lars Petter Jordheim (LP)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.

Emeline Perrial (E)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.

Eva-Laure Matera (EL)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.

Martine Caroff (M)

HEPHAISTOS-Pharma, Université Paris-Saclay, Orsay, France.

Jerome Kerzerho (J)

HEPHAISTOS-Pharma, Université Paris-Saclay, Orsay, France.

Charles Dumontet (C)

INSERM U1052, CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Lyon, France.
Hospices Civils de Lyon, Lyon, France.

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Classifications MeSH