Evidence map›Paper›PMID 39071806›Full record

ArticleFrontiers in cell and developmental biology2024

Piloting a scale-up platform for high-quality human T-cells production.

Viknesvaran Selvarajan, Denise Bei Lin Teo, Chaw-Chiea Chang, Yuen Ling Ng, Nge Cheong, Jaichandran Sivalingam, Soo Hean Gary Khoo, Adison Wong, Bernard Liat Wen Loo

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Scale-down bioreactors-comparative analysis of configurations.Bioprocess and biosystems engineering · 2025
    Review
  2. Article
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

9 authors.

Viknesvaran SelvarajanFood, Chemical and Biotechnology, Singapore Institute of Technology, Singapore, Singapore.
Denise Bei Lin TeoFood, Chemical and Biotechnology, Singapore Institute of Technology, Singapore, Singapore.
Chaw-Chiea ChangChemical Engineering, Newcastle University in Singapore, Singapore, Singapore.
Yuen Ling NgChemical Engineering, Newcastle University in Singapore, Singapore, Singapore.
Nge CheongQuintech Life Sciences Pte. Ltd., Singapore, Singapore.
Jaichandran SivalingamTessa Therapeutics Ltd., Singapore, Singapore.
Soo Hean Gary KhooTessa Therapeutics Ltd., Singapore, Singapore.
Adison WongFood, Chemical and Biotechnology, Singapore Institute of Technology, Singapore, Singapore.
Bernard Liat Wen LooFood, Chemical and Biotechnology, Singapore Institute of Technology, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell and gene therapies are an innovative solution to various severe diseases and unfulfilled needs. Adoptive cell therapy (ACT), a form of cellular immunotherapies, has been favored in recent years due to the approval of chimeric antigen receptor CAR-T products. Market research indicates that the industry's value is predicted to reach USD 24.4 billion by 2030, with a compound annual growth rate (CAGR) of 21.5%. More importantly, ACT is recognized as the hope and future of effective, personalized cancer treatment for healthcare practitioners and patients worldwide. The significant global momentum of this therapeutic approach underscores the urgent need to establish it as a practical and standardized method. It is essential to understand how cell culture conditions affect the expansion and differentiation of T-cells. However, there are ongoing challenges in ensuring the robustness and reproducibility of the manufacturing process. The current study evaluated various adoptive T-cell culture platforms to achieve large-scale production of several billion cells and high-quality cellular output with minimal cell death. It examined factors such as bioreactor parameters, media, supplements and stimulation. This research addresses the fundamental challenges of scalability and reproducibility in manufacturing, which are essential for making adoptive T-cell therapy an accessible and powerful new class of cancer therapeutics.

Indexed as

adoptive cell therapybiaxial rotary bioreactorbioprocessingscale-upstirred-tank bioreactorT-cell

Identifiers

PMID39071806
PMCPMC11282488

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.