bioRxivSynthetic BiologyPreprint
Secreted Particle Information Transfer (SPIT) - A Cellular Platform For In Vivo Genetic Engineering
Carsten T. CharlesworthiD, Shota HommaiD, Fabian Patrik SuchyiD, Sicong WangiD, Joydeep BhaduryiD, Anais K. AmayaiD, Joab CamarenaiD, Jinyu ZhangiD, Tze-Kai TaniD, Kyomi J. IgarashiiD, Hiromitsu NakauchiiD
Abstract
A multitude of tools now exist that allow us to precisely manipulate the human genome in a myriad of different ways. However, successful delivery of these tools to the cells of human patients remains a major barrier to their clinical implementation. Here we introduce a new cellular approach for in vivo genetic engineering, Secreted Particle Information Transfer (SPIT) that utilizes human cells as delivery vectors for in vivo genetic engineering. We demonstrate the application of SPIT for cell-cell delivery of Cre recombinase and CRISPR-Cas9 enzymes, we show that genetic logic can be incorporated into SPIT and present the first demonstration of human cells as a delivery platform for in vivo genetic engineering in immunocompetent mice. We successfully applied SPIT to genetically modify multiple organs and tissue stem cells in vivo including the liver, spleen, intestines, peripheral blood, and bone marrow. We anticipate that by harnessing the large packaging capacity of a human cells nucleus, the ability of human cells to engraft into patients long term and the capacity of human cells for complex genetic programming, that SPIT will become a paradigm shifting approach for in vivo genetic engineering.
- Citations
- 5
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Programming primary human T cells to deliver gene editing machinery
James Meixiong, Oleksandr Zginnyk, … Matthew H. Spitzer·bioRxiv·Oct 2, 2026
- Self-cutting and integrating CRISPR plasmids (SCIPs) enable targeted genomic integration of large genetic payloads for rapid cell engineering
D. Bloemberg, D. Sosa-Miranda, … S. McComb·bioRxiv·Mar 25, 2020
- Programmable enveloped delivery vehicles for human genome engineering in vivo
Jennifer R. Hamilton, Evelyn Chen, … Jennifer A. Doudna·bioRxiv·Aug 24, 2022
- A temperature-sensitive and interferon-silent Sendai virus vector for CRISPR-Cas9 delivery and gene editing in primary human cells
Christian S. Stevens, Jillian C. Carmichael, … Benhur Lee·Journal of VirologyPeer-reviewed·Nov 4, 2024
- Gene knock-outs in human CD34+ hematopoietic stem and progenitor cells and in the human immune system of mice
D. Kuppers, J. Linton, … P. PADDISON·bioRxiv·Oct 6, 2022
- Programming T cells for intercellular genome editing
Kevin M. Wasko, Madeleine Maker, … Jennifer A. Doudna·bioRxiv·Jun 23, 2026