Inflammasome activation, NLRP3 engagement and macrophage recruitment to tumor microenvironment are all required for Salmonella antitumor effect
Salmonella -based cancer therapies show great potential in preclinical models, but for most cases the observed antitumor effect is transient. Understanding the basis of the antitumor efficacy might guide the design of improved strains that elicit long-lasting effects, paving the wave for clinical us...
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Veröffentlicht in: | Cancer Immunology, Immunotherapy Immunotherapy, 2022-09, Vol.71 (9), p.2141-2150 |
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Sprache: | eng |
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Zusammenfassung: | Salmonella
-based cancer therapies show great potential in preclinical models, but for most cases the observed antitumor effect is transient. Understanding the basis of the antitumor efficacy might guide the design of improved strains that elicit long-lasting effects, paving the wave for clinical use. Here, we deepened into the role of macrophages and inflammasome activation in the context of
Salmonella
anti-melanoma effect. We showed inflammasome activation in melanoma cells upon infection, which correlated with cell surface exposure of gasdermin-D (GSDM-D) and calreticulin (CRT) and High mobility group box 1 protein (HMGB-1) release, suggesting immunogenic cell death, particularly pyroptosis.
Salmonella
infection upregulated levels of
Caspase-11
(
Casp11
) mRNA, but not
Nlrp3
or
Nlrc4
mRNA, the only described inflammasome receptors engaged by
Salmonella
, suggesting that non-canonical inflammasome activation could be occurring in melanoma cells. Intratumoral administration of
Salmonella
to melanoma-bearing mice elicited local inflammasome activation and interleukin-1β (IL-1β) production together with tumor growth retardation and extended survival in wild type but not
Caspase-1/11
(
Casp1/11
) knockout mice despite similar levels of intratumoral IL-1β in the later.
Salmonella
antitumor activity was also suppressed in melanoma bearing
Nlrp3
knockout mice.
Salmonella
induced macrophage recruitment to the tumor site and infiltrating cells exhibited inflammasome activation. Depletion experiments confirmed that macrophages are also essential for
Salmonella
anti-melanoma effect. Intratumoral macrophages showed a marked M2/M1 shift soon after treatment but this inflammatory profile is then lost, which could explain the transient effect of therapy. All in all, our results highlight CASP-1/11 axis and macrophages as essential players in
Salmonella
-based cancer immunotherapy and suggest a possible target for future interventions. |
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ISSN: | 0340-7004 1432-0851 |
DOI: | 10.1007/s00262-022-03148-x |