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Figure 3 from Antigen-Loaded Extracellular Vesicles Induce Responsiveness to Anti–PD-1 and Anti–PD-L1 Treatment in a Checkpoint Refractory Melanoma Model

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Le résumé fourni par la source

EVs alone or combined with checkpoint blockade treatment induces antigen-specific immune responses in a melanoma model. A, Mice with OVA-expressing B16 melanoma were treated with PBS or EVs intravenously and anti–PD-1/PD-L1 intraperitoneally as indicated. B, After inoculation, tumors were measured every 2 to 3 days, and mice were sacrificed when the tumors reached 1,000 mm3 in size. The results represent the mean size of the tumors in mice in each group (n = 10–14). Survival was plotted using a Kaplan–Meier survival curve. C, At the endpoint, tumors were collected and analyzed for immune cell infiltration using flow cytometry. Immune cells were identified as CD45+ and B16 melanoma cells as CD45−. * represents significance compared with the control group. D, B16 melanoma cells were analyzed for surface MHC class I and PD-L1 expression. E, The proportion of infiltrating total, CD8+ and antigen-specific T cells in tumors was analyzed by flow cytometry. F, PD-1 expression on the infiltrating CD8+ T cells was determined using flow cytometry. The graphs show the results of two independent experiments, with 4 to 5 mice per group. Dots represent a single mouse, and data are presented as the mean ± SD. Data were analyzed using the Kruskal–Wallis test with Dunn test for multiple comparisons. The Mantel–Cox test was applied for the survival curve. *, P < 0.05; **, P < 0.01; and ***, P < 0.001.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Figure 3 from Antigen-Loaded Extracellular Vesicles Induce Responsiveness to Anti–PD-1 and Anti–PD-L1 Treatment in a Checkpoint Refractory Melanoma Model
Date Crossref
26/11/2025
Éditeur
American Association for Cancer Research (AACR)
Type
posted-content

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Les sujets associés

Extracellular vesicles in diseaseNanoplatforms for cancer theranosticsCancer Immunotherapy and Biomarkers

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