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Data · dataset · 2026

Image 1_Pimozide enhances antigen cross-presentation and promotes cytotoxic CD8+ T cell immunity by stimulating dendritic cells.jpeg

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.3389/fimmu.2026.1946712.s002

<p>The activation of cytotoxic CD8<sup>+</sup> T cells requires antigen presentation in the context of major histocompatibility complex class I (MHC-I).

Description

While endogenous antigens can directly access this pathway, the priming of CD8<sup>+</sup> T cells against exogenous antigens—such as those derived from tumors or internalized pathogens—depends on dendritic cell (DC)-mediated antigen cross-presentation. Strategies capable of enhancing DC cross-presentation are therefore of considerable interest for the development of next-generation immunotherapies.

Here, we demonstrate that pimozide, a clinically approved antipsychotic with reported antitumoral and immunomodulatory properties, acts as a pharmacological enhancer of antigen cross-presentation. We show that pimozide-treated DCs display improved cross-presentation of soluble antigens, leading to stronger CD8<sup>+</sup> T cell activation and proliferation in vivo, enhanced IFN-γ production by antigen-specific CD8<sup>+</sup> T cells in vitro, and augmented cytotoxic T lymphocyte responses in vivo.

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Mechanistically, pimozide reshapes antigen-processing pathways in DCs by increasing reactive oxygen species production and altering endosomal physiology, thereby creating a biochemical environment that favors antigen cross-presentation. Moreover, pimozide treatment reduces STAT5 levels in DCs, and pharmacological inhibition of STAT5 with an independent inhibitor recapitulates the enhancement of cross-presentation and CD8<sup>+</sup> T cell activation, suggesting STAT5 signaling as a mediator of this effect.

Together, these findings reveal an unrecognized immunomodulatory activity of pimozide on DCs and establish a conceptual framework for the pharmacological repositioning of small molecules to reprogram DC function. This work ultimately opens new avenues for amplifying cytotoxic CD8<sup>+</sup> T cell immunity in the context of next-generation cancer immunotherapies.</p>

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Cancer 75% · Image 75%
Provenance · 3 source records, 13 field assertions
SourceKeyLast seenRaw
ZivaHuboai:figshare.com:article/3403938012 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/3403938012 d agoJSON v1
DMU Figshareoai:figshare.com:article/3403938012 d agoJSON v1
FieldAssertionExtractorEvidence
access_levelsource · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0
concepts[disease].local:disease:cancerenrichment · zivahub uct ac zakeyword-concept-rules@1.0.0title+description (75%)
concepts[field].local:field:earth-environmentalmapping · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0
concepts[field].local:field:earth-environmentalmapping · figshare dmu ac ukconnector:figshare_dmu_ac_uk@1.0.0
concepts[field].local:field:earth-environmentalmapping · dro deakin edu auconnector:dro_deakin_edu_au@1.0.0
concepts[field].local:field:life-sciencesmapping · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0
concepts[field].local:field:life-sciencesmapping · dro deakin edu auconnector:dro_deakin_edu_au@1.0.0
concepts[field].local:field:life-sciencesmapping · figshare dmu ac ukconnector:figshare_dmu_ac_uk@1.0.0
concepts[modality].local:modality:imageenrichment · zivahub uct ac zakeyword-concept-rules@1.0.0title+description (75%)
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