Author

G. Dotti

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Immunology· 3 Cancer Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell type annotation· 3 Organism:human· 3 Organism:mouse· 3 Assay:proteomics· 3 Research Focus:cancer & tumor microenvironment· 2 Research Focus:drug response / drug discovery· 2 Research Focus:cell-cell communication· 1

Frequent Co-Authors

B. Savoldo· 3 shared A. Ottaviani· 2 shared C. Cenciarelli· 2 shared D. Lauro· 2 shared E. Landoni· 2 shared G. Lanzilli· 2 shared G. Sconocchia· 2 shared R. Arriga· 2 shared

Activity by Year

2019-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersImmunology

B. Savoldo

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

CSPG4-targeting CAR-macrophages inhibit melanoma growth

D. Greiner, Q. Xue, T. Q. Waddell, E. Kurudza, R. L. Belote, G. Dotti, R. L. Judson-Torres, M. Q. Reeves, S. H. Cheshier, M. Roh-Johnson

This study engineers CSPG4-targeting CAR-macrophages that inhibit melanoma growth in vitro and in vivo, showing promise for solid tumor immunotherapy.

bioRxiv · Jun 4, 2024 · PreprintCancer Biology

Atlas-Guided Discovery of Transcription Factors for T Cell Programming

H. K. Chung, C. Liu, A. Battu, A. N. Jambor, B. M. Pratt, F. Xie, B. P. Riesenberg, E. Casillas, M. Sun, E. Landoni, Y. Li, Q. Ye, D. Joo, J. Green, Z. Syed, , S. M. Kaech

The paper identifies transcription factors driving distinct CD8+ T cell states and shows their impact on tumor control and immunotherapy.

bioRxiv · Jan 3, 2023Immunology

Inadvertent Transfer of Murine VL30 Retrotransposons to CAR-T Cells.

S. h. Lee, Y. Hao, T. Gui, G. Dotti, B. Savoldo, F. Zou, T. Kafri

This study shows that murine VL30 retrotransposons can be inadvertently transferred to CAR-T cells via γ-retroviral vectors, raising biosafety concerns.

bioRxiv · Feb 1, 2022Microbiology

CD16-158-VALINE CHIMERIC RECEPTOR T CELLS OVERCOME THE RESISTANCE OF KRAS-MUTATED COLORECTAL CARCINOMA CELLS TO CETUXIMAB

R. Arriga, S. Caratelli, G. Lanzilli, A. Ottaviani, C. Cenciarelli, T. Sconocchia, G. C. Spagnoli, G. Iezzi, M. Roselli, D. Lauro, G. Dotti, S. Ferrone, G. Sconocchia

This study evaluates CD16-158-VALINE chimeric receptor T cells for overcoming cetuximab resistance in KRAS-mutated colorectal cancer, finding they enhance IFNγ and TNF release and control tumor growth in mice.

bioRxiv · Mar 26, 2019Immunology

ELIMINATION OF EGFR-OVEREXPRESSING CANCER CELLS BY CD32 CHIMERIC RECEPTOR T CELLS IN COMBINATION WITH CETUXIMAB OR PANITUMUMAB

S. Caratelli, R. Arriga, T. Sconocchia, A. Ottaviani, G. Lanzilli, D. Pastore, C. Cenciarelli, A. Venditti, M. I. Del Principe, D. Lauro, E. Landoni, H. Du, B. Savoldo, S. Ferrone, G. Dotti, G. Sconocchia

This study shows CD32131R-CR T cells can eliminate EGFR-overexpressing cancer cells when combined with cetuximab or panitumumab, outperforming CD16158F-CR T cells.

bioRxiv · Mar 18, 2019 · PreprintImmunology