Preventive cancer vaccination with P5 HER-2/neo-derived peptide-pulsed peripheral blood mononuclear cells in a mouse model of breast cancer.
Animals
Apoptosis
Breast Neoplasms
/ metabolism
Cancer Vaccines
/ administration & dosage
Cell Proliferation
Disease Models, Animal
Female
Humans
Leukocytes, Mononuclear
/ metabolism
Mice
Mice, Inbred BALB C
Mice, Nude
Peptide Fragments
/ administration & dosage
Receptor, ErbB-2
/ immunology
Tumor Cells, Cultured
Vaccination
Xenograft Model Antitumor Assays
active immunity
breast cancer
cancer du sein
cellules dendritiques
cellules mononucléaires du sang périphérique
dendritic cells
immunité active
peptide vaccine
peripheral blood mononuclear cells
vaccin peptidique
Journal
Biochemistry and cell biology = Biochimie et biologie cellulaire
ISSN: 1208-6002
Titre abrégé: Biochem Cell Biol
Pays: Canada
ID NLM: 8606068
Informations de publication
Date de publication:
08 2021
08 2021
Historique:
pubmed:
5
1
2021
medline:
29
9
2021
entrez:
4
1
2021
Statut:
ppublish
Résumé
This study compared the prophylactic effects from vaccines based on dendritic cells (DCs) and peripheral blood mononuclear cells (PBMCs) by pulsing the cells in-vitro with p5 peptide. The different test groups of mice were injected with free peptide or with peptide pulsed with DCs or PBMCs. Two weeks after the last booster dose, immunological tests were performed on splenocyte suspensions from three mice in each group and the remaining mice (5/each group) were evaluated for tumor growth and survival time. The levels of IFN-γ, granzyme B, and IL-10 were detected in T cells. Additionally, IFN-γ and perforin as well as mRNA levels of some genes associated with immune responses were assessed after challenging the splenocytes with TUBO cells. A significant increase was observed in frequency of CD4
Identifiants
pubmed: 33395361
doi: 10.1139/bcb-2020-0559
doi:
Substances chimiques
Cancer Vaccines
0
Peptide Fragments
0
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM