Evidence map›Paper›PMID 38462954›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2024

Gene Delivery From Granular Scaffolds for Tunable Biologics Manufacturing.

Evan Kurt, Garth Devlin, Aravind Asokan, Tatiana Segura

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Evan KurtDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.ORCID 0000-0002-5402-373X
Garth DevlinDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
Aravind AsokanDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.ORCID 0000-0001-5563-4877
Tatiana SeguraDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.ORCID 0000-0003-1569-8686

Funding

University Training Program in Biomolecular & Tissue EngineeringT32GM008555 · NIGMS · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 1994 to 2021
$8.1M
VEGF Ligand Presentation and Therapeutic AngiogenesisR01NS079691 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SEGURA, TATIANA · 2012 to 2024
$4.0M
Biomaterials to promote synapse formation after strokeR01NS112940 · NINDS · DUKE UNIVERSITY · PI Tatiana Segura · 2020 to 2026
$3.9M
Engineering Adaptive Immune Responses from Hydrogel Scaffolds to Promote Tissue RegenerationR01AI152568 · NIAID · DUKE UNIVERSITY · PI COLLIER, JOEL H, SEGURA, TATIANA · 2020 to 2024
$3.2M
University Training Program in Biomolecular and Tissue EngineeringT32GM144291 · NIGMS · DUKE UNIVERSITY · PI Charles A. Gersbach, Tatiana Segura · 2022 to 2026
$2.6M
Engineering Injectable Microporous Hydrogels for Brain RepairR01NS094599 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SEGURA, TATIANA · 2016 to 2019
$1.5M
NIAID NIH HHS R01 AI152568NIGMS NIH HHS T32 GM008555NIGMS NIH HHS T32 GM144291NIH HHS R01NS094599NIH National Service Research Awards T32GM008555NINDS NIH HHS R01 NS079691NINDS NIH HHS R01 NS094599NINDS NIH HHS R01 NS112940
6 · The paper itself

Abstract

The understanding of the molecular basis for disease has generated a myriad of therapeutic biologics, including therapeutic proteins, antibodies, and viruses. However, the promise that biologics can resolve currently incurable diseases hinges in their manufacturability. These therapeutics require that their genetic material be introduced to mammalian cells such that the cell machinery can manufacture the biological components. These are then purified, validated, and packaged. Most manufacturing uses batch processes that collect the biologic a few days following genetic modification, due to toxicity or difficulty in separating product from cells in a continuous operation, limiting the amount of biologic that can be produced and resulting in yearlong backlogs. Here, a scaffold-based approach for continuous biologic manufacturing is presented, with sustained production of active antibodies and viruses for 30 days. The use of scaffold-based biologic production enabled perfusion-based bioreactors to be used, which can be incorporated into a fully continuous process.

Indexed as

Biological ProductsGene Transfer TechniquesAnimalsBioreactorsCHO CellsCricetulusHumansTissue ScaffoldsBiological ProductsAAVantibodyhydrogelmanufacturingtransfection

Identifiers

PMID38462954
PMCPMC11294003

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.