T
Timothy L. Ratliff
Researcher at Purdue University
Publications - 312
Citations - 20541
Timothy L. Ratliff is an academic researcher from Purdue University. The author has contributed to research in topics: Prostate cancer & Cancer. The author has an hindex of 69, co-authored 306 publications receiving 19092 citations. Previous affiliations of Timothy L. Ratliff include University of Iowa Hospitals and Clinics & Beth Israel Deaconess Medical Center.
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Journal ArticleDOI
Folate Receptor Beta Designates Immunosuppressive Tumor-Associated Myeloid Cells that Can Be Reprogrammed with Folate-Targeted Drugs.
Gregory M. Cresswell,Bingbing Wang,Erin M. Kischuk,Meaghan M. Broman,Rami A. Alfar,Renee E. Vickman,Dimiter S. Dimitrov,Sumith A. Kularatne,Chandru P. Sundaram,Sunil Singhal,Evgeniy Eruslanov,Scott A. Crist,Bennett D. Elzey,Timothy L. Ratliff,Philip S. Low +14 more
TL;DR: The data reveal a broadly applicable strategy across tumor types for reprogramming MDSCs and TAMs into antitumorigenic immune cells using a drug that would otherwise be too toxic to administer systemically and establish FRβ as the first marker that distinguishes immunosuppressive from nonimmunosuppression subsets of M DSCs and AMs.
Journal ArticleDOI
Strategy for improving therapy of superficial bladder cancer
Timothy L. Ratliff,Timothy L. Ratliff,M'Liss A. Hudson,M'Liss A. Hudson,William J. Catalona,William J. Catalona +5 more
TL;DR: It is believed that BCG is the current "gold standard" for the treatment of superficial bladder cancer; as such, improvements in BCG therapy would constitute improvement in the treatment and/or developing alternative therapeutic approaches.
Journal ArticleDOI
1α, 25 Dihydroxyvitamin D (1,25(OH)2D) inhibits the T cell suppressive function of myeloid derived suppressor cells (MDSC)
TL;DR: The data suggest that activation of vitamin D signaling could be used to suppress MDSC function and release a constraint on T-cell mediated clearance of TU cells.
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Cell-intrinsic abrogation of TGF-β signaling delays but does not prevent dysfunction of self/tumor-specific CD8 T cells in a murine model of autochthonous prostate cancer
Cassie K. Chou,Andrea Schietinger,H. Denny Liggitt,Xiaoxia Tan,Sarah E. Funk,Gordon J. Freeman,Timothy L. Ratliff,Norman M. Greenberg,Philip D. Greenberg,Philip D. Greenberg +9 more
TL;DR: It is found that persistence and antitumor activity of adoptively transferred effector T cells deficient in TGF-β signaling were significantly improved in the cancerous prostate, however, over time, despite persistence in peripheral lymphoid organs, the numbers of transferred cells in the prostate decreased and the residual prostate-infiltrating T cells were no longer functional.
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Evaluation of gene transfer efficiency by viral vectors to murine bladder epithelium
TL;DR: Significant differences in gene expression are achieved by varying physical parameters during intravesical instillation, and increased gene expression associated with larger volume instillation may be responsible for some reported variability of gene transfer to the bladder.