In situ vaccination via tissue-targeted cDC1 expansion enhances the immunogenicity of chemoradiation and immunotherapy is a research paper published in Journal of Clinical Investigation (2023). On theSindex it has a DataRank of 0. It has been cited 21 times.
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National Cancer Institute Specialized Program of Research Excellence (SPORE) in Cervical Cancer
Grant: NIH/NCI P50A098252
National Cancer Institute
Grant: R01CA237067
National Cancer Institute
Grant: R21DE029910-01
National Cancer Institute
Grant: R21CA256020
National Cancer Institute
Grant: 1R21CA234516-01A1
Albumin-FMS-like tyrosine kinase 3 ligand (Alb-Flt3L) fusion protein as a novel adjuvant to enhance the immunogenicity and therapeutic and prophylactic efficacies of a HPV protein vaccine
NIH-supported career development fellowship
Grant: 5F31CA236051
NCI NIH HHS
Grant: R21 CA234516
NCI NIH HHS
Grant: F31 CA236051
NIDCR NIH HHS
Grant: R21 DE029910
NCI NIH HHS
Grant: P50 CA098252
National Institutes of Health
Grant: 5R01CA237067-05
Development of Novel Spontaneous HPV Cervicovaginal Carcinoma Models for Cancer Immunotherapy
National Institutes of Health
Grant: 1F31CA236051-01
The role of Albumin-Flt3L-induced cross-presenting dendritic cell expansion in antitumor immunity
National Institutes of Health
Grant: 5R21DE029910-02
Novel immunotherapeutic regimen combining the dendritic cell expansion power of Albumin-Flt3L and inflammatory cues of Salmonella
National Institutes of Health
Grant: 5P50CA098252-17
SPORE in Cervical Cancer
National Institutes of Health
Grant: 1R21CA256020-01A1
Novel strategy combined with targeted radiation therapy unleashes potent antitumor immunity in HPV + head and neck cancer
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Additional file 1 of FLT3L-induced virtual memory CD8 T cells engage the immune system against tumors
Additional file 1 of FLT3L-induced virtual memory CD8 T cells engage the immune system against tumors