Evidence map›Paper›PMID 39484520›Full record

ArticlebioRxiv : the preprint server for biology2024

Orthogonalized human protease control of secreted signals.

Carlos A Aldrete, Connor C Call, Lucas E Sant'Anna, Alexander E Vlahos, Jimin Pei, Qian Cong, Xiaojing J Gao

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Carlos A AldreteDepartment of Chemical Engineering, Stanford University, Stanford CA 94305, USA.ORCID 0000-0003-3795-4572
Connor C CallDepartment of Chemical Engineering, Stanford University, Stanford CA 94305, USA.ORCID 0000-0003-2394-7523
Lucas E Sant'AnnaDepartment of Bioengineering, Stanford University, Stanford CA 94305, USA.
Alexander E VlahosDepartment of Chemical Engineering, Stanford University, Stanford CA 94305, USA.ORCID 0000-0002-2154-8791
Jimin PeiEugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-3505-9665
Qian CongEugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-8909-0414
Xiaojing J GaoDepartment of Chemical Engineering, Stanford University, Stanford CA 94305, USA.ORCID 0000-0002-3094-1456

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Synthetic DNA-free Circuits for “Scarless” Programming of Mammalian CellsR00EB027723 · NIBIB · STANFORD UNIVERSITY · PI GAO, XIAOJING J · 2020 to 2022
$747k
NIBIB NIH HHS R00 EB027723NIGMS NIH HHS T32 GM007276
6 · The paper itself

Abstract

Synthetic circuits that regulate protein secretion in human cells could support cell-based therapies by enabling control over local environments. While protein-level circuits enable such potential clinical applications, featuring orthogonality and compactness, their non-human origin poses a potential immunogenic risk. Here, we developed Humanized Drug Induced Regulation of Engineered CyTokines (hDIRECT) as a platform to control cytokine activity exclusively using human-derived proteins. We sourced a specific human protease and its FDA-approved inhibitor. We engineered cytokines (IL-2, IL-6, and IL-10) whose activities can be activated and abrogated by proteolytic cleavage. We utilized species specificity and re-localization strategies to orthogonalize the cytokines and protease from the human context that they would be deployed in. hDIRECT should enable local cytokine activation to support a variety of cell-based therapies such as muscle regeneration and cancer immunotherapy. Our work offers a proof of concept for the emerging appreciation of humanization in synthetic biology for human health.

Identifiers

PMID39484520
PMCPMC11526856

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.