Evidence map›Paper›PMID 41466308›Full record

ArticleJournal of biological engineering2025

Development of predictable and high-yield CHO cell line by site-specific integration.

Wanjun Lan, Xiaoli Yang, Juanjuan Yao, Lung-Jr Lin, Wenzheng Li, Weihai Chen, Jiangping Li, Qi Shen, Kang Li, Huiling Li and 3 more

Abstract read
In one paragraph

Article in Journal of biological engineering, 2025. 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. 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

13 authors.

Wanjun LanGreat Bay Bio Limited, Unit 518 of the 5th Floor of Building 11W, Phase Two, Hong Kong Science Park, Pak Shek Kok, New Territories, Hong Kong, China.
Xiaoli YangShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Juanjuan YaoShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Lung-Jr LinGreat Bay Bio Limited, Unit 518 of the 5th Floor of Building 11W, Phase Two, Hong Kong Science Park, Pak Shek Kok, New Territories, Hong Kong, China.
Wenzheng LiShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Weihai ChenShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Jiangping LiShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Qi ShenShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Kang LiShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Huiling LiShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Yujia ChenShenzhen Taili Biotechnology Co., Ltd., No. 323-M, 3rd Floor, Zonghe Xinxing I, No. 1 Haihong Road, Fubao Community, Fubao Subdistrict, Futian District, Shenzhen City, China.
Liang ChenGreat Bay Bio Limited, Unit 518 of the 5th Floor of Building 11W, Phase Two, Hong Kong Science Park, Pak Shek Kok, New Territories, Hong Kong, China. liang.chen@greatbay-bio.com.
Kingsley LeungGreat Bay Bio Limited, Unit 518 of the 5th Floor of Building 11W, Phase Two, Hong Kong Science Park, Pak Shek Kok, New Territories, Hong Kong, China. kingsley@greatbay-bio.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chinese hamster ovary (CHO) cell is a widely used cell line for the production of therapeutic proteins. Customarily, CHO host cell line is established through random integration, which requires multiple rounds of screening to identify the optimal producer. In contrast, site-specific integration (SSI) technology can boost cell line development efficiency by directing gene of interest (GOI) to certain genomic loci that supports sustained and stable expression. In this study, by utilizing AI algorithms and robotic systems, we have identified several CHO host cell lines carrying marker gene by Bxb1-mediated SSI technology. After the substitution of marker gene with different types of GOI at specific sites, some of cases delivered a titer exceeding 15 g/L. Thanks to the uniformity of SSI cell lines, protein titer and quality of monoclonal cells can be predicted based on the performance of corresponding minipools. Different monoclonal cells originated from the same minipool also showed consistent protein quality. Furthermore, it was observed that the monoclonal cells obtained by SSI demonstrated consistency in protein titer, quality and genetic stability after 26 consecutive passages (approximately 90 days). In summary, we have successfully developed an effective platform for the construction of SSI cell lines, which allows the rapid and efficient expression of various proteins while maintaining consistency in stability and product quality.

Indexed as

Bxb1 integraseCHO cell lineSite-specific integration (SSI)

Identifiers

PMID41466308
PMCPMC12860097

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.