Evidence map›Paper›PMID 40014418›Full record

ReviewEssays in biochemistry2025

Engineered bacteria and bacterial derivatives as advanced therapeutics for inflammatory bowel disease.

Jingyuan Wu, Wanlin Ye, Jie Yu, Tuoyu Zhou, Nuo Zhou, Dennis K P Ng, Zhaoting Li

Abstract readReview
In one paragraph

Review in Essays in biochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

7 authors.

Jingyuan Wu *School of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong, 518172, P. R. China.
Wanlin Ye *School of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong, 518172, P. R. China.
Jie YuSchool of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong, 518172, P. R. China.
Tuoyu ZhouSchool of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong, 518172, P. R. China.
Nuo ZhouSchool of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong, 518172, P. R. China.
Dennis K P NgDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, N. T., Hong Kong, P. R. China.
Zhaoting LiSchool of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong, 518172, P. R. China.ORCID 0000-0002-4596-9603

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD), a chronic and relapsing-remitting condition, is inadequately managed by conventional therapies that often lack targeting specificity and carry significant side effects, particularly failing to address intestinal barrier repair and microbial balance. Probiotics, with their strong colonization capabilities, present a novel approach to drug delivery. Various engineering strategies have been developed to enhance the targeting ability of probiotics to inflammation sites, enabling precise delivery or in situ synthesis of therapeutic molecules to expand their multifunctional potential. This review discusses the recent advancements in bacterial modifications, including surface physico-chemical and biological coating, genetic engineering, outer membrane vesicles, minicells, and bacterial ghosts, all of which can enhance therapeutic localization. We also outline critical preclinical considerations, such as delivery frequency, systemic distribution, immune evasion, and gene contamination risks, for clinical translation. These engineered bacteria and bacterial derivatives hold great promise for personalized and sustained IBD treatments, providing a new frontier for therapy tailored to the complex inflammatory environment of IBD.

Indexed as

BacteriaInflammatory Bowel DiseasesProbioticsAnimalsDrug Delivery SystemsGenetic EngineeringHumansengineered bacteriainflammatory bowel diseaseoral delivery systemouter membrane vesiclessynthetic biology

Identifiers

PMID40014418
PMCPMC12203993

What OpenQuestion holds

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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.