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WT1 Pulsed Human CD141+ Dendritic Cell Vaccine Has High Potential in Solid Tumor-Targeted Immunotherapy
DC Field | Value | Language |
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dc.contributor.author | Cho, SY | - |
dc.contributor.author | Jeong, SM | - |
dc.contributor.author | Jeon, YJ | - |
dc.contributor.author | Yang, SJ | - |
dc.contributor.author | Hwang, JE | - |
dc.contributor.author | Yoo, BM | - |
dc.contributor.author | Kim, HS | - |
dc.date.accessioned | 2023-05-23T04:04:21Z | - |
dc.date.available | 2023-05-23T04:04:21Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/25546 | - |
dc.description.abstract | Dendritic cells (DC) are powerful cells that play critical roles in anti-tumor immunity, and their use in cancer immunotherapy unlocks hidden capabilities as an effective therapeutic. In order to maximize the full potential of DC, we developed a DC vaccine named CellgramDC-WT1 (CDW). CDW was pulsed with WT1, an antigen commonly expressed in solid tumors, and induced with zoledronate to aid DC maturation. Although our previous study focused on using Rg3 as an inducer of DC maturation, problems with quality control and access led us to choose zoledronate as a better alternative. Furthermore, CDW secreted IL-12 and IFN-γ, which induced the differentiation of naïve T cells to active CD8+ T cells and elicited cytotoxic T lymphocyte (CTL) response against cancer cells with WT1 antigens. By confirming the identity and function of CDW, we believe CDW is an improved DC vaccine and holds promising potential in the field of cancer immunotherapy. | - |
dc.language.iso | en | - |
dc.subject.MESH | Cancer Vaccines | - |
dc.subject.MESH | Dendritic Cells | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Immunotherapy | - |
dc.subject.MESH | Neoplasms | - |
dc.subject.MESH | T-Lymphocytes, Cytotoxic | - |
dc.subject.MESH | Vaccines | - |
dc.subject.MESH | WT1 Proteins | - |
dc.subject.MESH | Zoledronic Acid | - |
dc.title | WT1 Pulsed Human CD141+ Dendritic Cell Vaccine Has High Potential in Solid Tumor-Targeted Immunotherapy | - |
dc.type | Article | - |
dc.identifier.pmid | 36675017 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864659 | - |
dc.subject.keyword | cancer antigens | - |
dc.subject.keyword | cancer immunotherapy | - |
dc.subject.keyword | CD141 | - |
dc.subject.keyword | DC vaccine | - |
dc.subject.keyword | dendritic cells | - |
dc.subject.keyword | solid tumor | - |
dc.subject.keyword | T-cell activation | - |
dc.subject.keyword | tumor-associated antigens | - |
dc.subject.keyword | Wilms’ tumor1 (WT1) | - |
dc.subject.keyword | zoledronate | - |
dc.contributor.affiliatedAuthor | Yoo, BM | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.3390/ijms24021501 | - |
dc.citation.title | International journal of molecular sciences | - |
dc.citation.volume | 24 | - |
dc.citation.number | 2 | - |
dc.citation.date | 2023 | - |
dc.citation.startPage | 1501 | - |
dc.citation.endPage | 1501 | - |
dc.identifier.bibliographicCitation | International journal of molecular sciences, 24(2). : 1501-1501, 2023 | - |
dc.identifier.eissn | 1422-0067 | - |
dc.relation.journalid | J014220067 | - |
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