Framework for in vivo T cell screens

In vivo T cell screens are a powerful tool for elucidating complex mechanisms of immunity, yet there is a lack of consensus on the screen design parameters required for robust in vivo screens: gene library size, cell transfer quantity, and number of mice. Here, we describe the Framework for In vivo...

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Veröffentlicht in:The Journal of experimental medicine 2024-04, Vol.221 (4)
Hauptverfasser: Milling, Lauren E, Markson, Samuel C, Tjokrosurjo, Qin, Derosia, Nicole M, Streeter, Ivy S L, Hickok, Grant H, Lemmen, Ashlyn M, Nguyen, Thao H, Prathima, Priyamvada, Fithian, William, Schwartz, Marc A, Hacohen, Nir, Doench, John G, LaFleur, Martin W, Sharpe, Arlene H
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Sprache:eng
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Zusammenfassung:In vivo T cell screens are a powerful tool for elucidating complex mechanisms of immunity, yet there is a lack of consensus on the screen design parameters required for robust in vivo screens: gene library size, cell transfer quantity, and number of mice. Here, we describe the Framework for In vivo T cell Screens (FITS) to provide experimental and analytical guidelines to determine optimal parameters for diverse in vivo contexts. As a proof-of-concept, we used FITS to optimize the parameters for a CD8+ T cell screen in the B16-OVA tumor model. We also included unique molecular identifiers (UMIs) in our screens to (1) improve statistical power and (2) track T cell clonal dynamics for distinct gene knockouts (KOs) across multiple tissues. These findings provide an experimental and analytical framework for performing in vivo screens in immune cells and illustrate a case study for in vivo T cell screens with UMIs.
ISSN:0022-1007
1540-9538
1540-9538
DOI:10.1084/jem.20230699