Protocol to prepare MUC1 glycopeptide vaccines and evaluate immunization effects in mice

The tumor-associated mucin MUC1 is overexpressed in almost all types of epithelial tumor tissues, making it an attractive target antigen for cancer immunotherapy. Here we present a protocol to prepare MUC1 glycopeptide vaccines and to evaluate immunization effects in mice. We describe steps for synt...

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Veröffentlicht in:STAR protocols 2024-06, Vol.5 (2), p.103047, Article 103047
Hauptverfasser: Wu, Ye, Zhou, Yang, Guo, Yajing, Ling, Yi, Li, Yiliang, Cai, Hui
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Sprache:eng
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Zusammenfassung:The tumor-associated mucin MUC1 is overexpressed in almost all types of epithelial tumor tissues, making it an attractive target antigen for cancer immunotherapy. Here we present a protocol to prepare MUC1 glycopeptide vaccines and to evaluate immunization effects in mice. We describe steps for synthesizing glycopeptide antigen and conjugating it with carrier protein to make vaccine candidates. We then detail procedures for mice immunization, antibody response evaluation, and cellular immune response. For complete details on the use and execution of this protocol, please refer to Cai et al.1,2 [Display omitted] •Prepare tumor-associated glycopeptide antigen by SPPS•Prepare vaccine candidates using protein carrier to increase glycopeptide immunogenicity•Evaluate vaccine effect by antibody potency and cellular immune response Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics. The tumor-associated mucin MUC1 is overexpressed in almost all types of epithelial tumor tissues, making it an attractive target antigen for cancer immunotherapy. Here we present a protocol to prepare MUC1 glycopeptide vaccines and to evaluate immunization effects in mice. We describe steps for synthesizing glycopeptide antigen and conjugating it with carrier protein to make vaccine candidates. We then detail procedures for mice immunization, antibody response evaluation, and cellular immune response.
ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2024.103047