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EXP002462

Paper

Neoantigen-specific mRNA/DC vaccines for effective anticancer immunotherapy (2024)

Peptide

RALA

Sequence: WEARLARALARALARHLARALARALRACEA

RNA

mRNA

All experiment fields

Experiment Id EXP002462
Paper Neoantigen-specific mRNA/DC vaccines for effective anticancer immunotherapy
Peptide RALA
Delivery Success Class yes
In Vivo Flag yes
Uptake Confirmed no
Label Confidence high
In Vitro Functional Effect
Endosomal Escape Evidence
Peptide Concentration Set by N/P ratio (N/P=10 used for subsequent studies); exact mass/µM not reported
Rna Concentration 2.5 µg mRNA complex added to BMDCs for 24 h (50 µL complex to cells)
Mixing Ratio N/P = 10
Formulation Format Ex vivo DC loading (neoantigen-mRNA/RALA) → DC vaccine
Formulation Components RALA + neoantigen mRNA polyplex; bone-marrow-derived DCs; GM-CSF/IL-4 culture; LPS maturation
Size Nm
Zeta Mv 26.20
Model Scope in_vivo
Model Type in vivo
Cell Lines Or Primary Cells Primary bone-marrow-derived DCs (C57BL/6) used as vaccine cells
Animal Model C57BL/6 male mice with MC38 subcutaneous tumors
Administration Route Subcutaneous injections of DC vaccine on days 7, 14, 21 post tumor inoculation (plus group with adoptive TIL)
Output Type Antitumor efficacy (tumor volume/weight); immune readouts (CD8+ IFN-γ+ infiltration, cytokines)
Output Value Tumor volume reduced vs PBS: ~606±43 mm³ (NeoAg-mRNA/DC) and ~391±74 mm³ (NeoAg-mRNA/DC + TIL) vs ~1433±65 mm³ (PBS)
Output Units
Output Notes Significant tumor growth inhibition; increased CD4+IFN-γ+ and CD8+IFN-γ+ TILs; increased serum IL-6, IL-12p70, TNF-α, IFN-γ
Toxicity Notes No significant body-weight loss; no reported toxic/side effects in treated groups
Curation Notes