Macrophages directly kill bladder cancer cells through TNF signaling as an early response to BCG therapy.


Journal

Disease models & mechanisms
ISSN: 1754-8411
Titre abrégé: Dis Model Mech
Pays: England
ID NLM: 101483332

Informations de publication

Date de publication:
01 Aug 2024
Historique:
received: 05 01 2024
accepted: 09 06 2024
medline: 8 8 2024
pubmed: 8 8 2024
entrez: 8 8 2024
Statut: ppublish

Résumé

The Bacillus Calmette-Guérin (BCG) vaccine is the oldest cancer immunotherapeutic agent in use. Despite its effectiveness, its initial mechanisms of action remain largely unknown. Here, we elucidate the earliest cellular mechanisms involved in BCG-induced tumor clearance. We developed a fast preclinical in vivo assay to visualize in real time and at single-cell resolution the initial interactions among bladder cancer cells, BCG and innate immunity using the zebrafish xenograft model. We show that BCG induced the recruitment and polarization of macrophages towards a pro-inflammatory phenotype, accompanied by induction of the inflammatory cytokines tnfa, il1b and il6 in the tumor microenvironment. Macrophages directly induced apoptosis of human cancer cells through zebrafish TNF signaling. Macrophages were crucial for this response as their depletion completely abrogated the BCG-induced phenotype. Contrary to the general concept that macrophage anti-tumoral activities mostly rely on stimulating an effective adaptive response, we demonstrate that macrophages alone can induce tumor apoptosis and clearance. Thus, our results revealed an additional step to the BCG-induced tumor immunity model, while providing proof-of-concept experiments demonstrating the potential of this unique model to test innate immunomodulators.

Identifiants

pubmed: 39114912
pii: 361492
doi: 10.1242/dmm.050693
pii:
doi:

Substances chimiques

BCG Vaccine 0
Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fundação Champalimaud
ID : RC168
Organisme : Lisbon Regional Operational Programme
ID : LISBOA-01-0145-FEDER-022170
Organisme : Fundação para a Ciência e a Tecnologia
ID : FCT-PTDC/MEC-ONC/31627/2017
Organisme : Calouste Gulbenkian Foundation

Informations de copyright

© 2024. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interests S.H.E.K. is co-inventor and co-holder of a patent for the TB vaccine VPM1002, which has been licensed to Vakzine Projekt Management GmbH, Hannover and Serum Institute of India Ltd., Pune, India. The remaining authors declare no competing or financial interests.

Auteurs

Mayra Fernanda Martínez-López (MF)

Cancer Research Group (CRG), Faculty of Medicine, Universidad de las Américas, Quito 170124, Ecuador.

Cátia Rebelo de Almeida (CR)

Champalimaud Research, Champalimaud Foundation, Av. Brasilia, Lisbon 1400-038, Portugal.

Márcia Fontes (M)

Champalimaud Research, Champalimaud Foundation, Av. Brasilia, Lisbon 1400-038, Portugal.

Raquel Valente Mendes (RV)

Champalimaud Research, Champalimaud Foundation, Av. Brasilia, Lisbon 1400-038, Portugal.

Stefan H E Kaufmann (SHE)

Max Planck Institute for Infection Biology, Berlin 10117, Germany.
Max Planck Institute for Multidisciplinary Sciences, Göttingen 37077, Germany.
Hagler Institute for Advanced Study, Texas A&M University, College Station, TX 77843, USA.

Rita Fior (R)

Champalimaud Research, Champalimaud Foundation, Av. Brasilia, Lisbon 1400-038, Portugal.

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Classifications MeSH