Evidence map›Paper›PMID 41800924›Full record

ArticleDisease models & mechanisms2026

A yeast synthetic biotic platform for delivery of therapeutic nanobodies to ameliorate gastrointestinal inflammation.

Roger Palou, Almer M van der Sloot, Aline A Fiebig, Megan T Zangara, Naseer Sangwan, María Sánchez-Osuna, Bushra Ilyas, Haley Zubyk, Michael Cook, Gerard D Wright and 2 more

Abstract read
In one paragraph

Article in Disease models & mechanisms, 2026. 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

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

12 authors.

Roger PalouProgram in Molecular Medicine, The Hospital for Sick Children Research Institute, Toronto, ON M5G 0A4, Canada.ORCID 0000-0001-7674-9358
Almer M van der SlootMila - Québec Artificial Intelligence Institute, Montréal, QC H2S 3H1, Canada.ORCID 0000-0003-0049-2044
Aline A FiebigDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Megan T ZangaraDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Naseer SangwanMicrobial Sequencing and Analytics Resource (MSAAR) Facility, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44106, USA.
María Sánchez-OsunaProgram in Molecular Medicine, The Hospital for Sick Children Research Institute, Toronto, ON M5G 0A4, Canada.
Bushra IlyasDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Haley ZubykDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Michael CookDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Gerard D WrightDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.ORCID 0000-0002-9129-7131
Brian K CoombesDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.ORCID 0000-0001-9883-1010
Mike TyersProgram in Molecular Medicine, The Hospital for Sick Children Research Institute, Toronto, ON M5G 0A4, Canada.ORCID 0000-0002-9713-9994

Funding

CIHR FDN-167277CIHR PJT-180315Genome CanadaGenome QuebecWeston Family Foundation
6 · The paper itself

Abstract

Protein-based pharmaceuticals, such as engineered antibodies, form a major drug class of steadily increasing market share. However, these biologic medicines are costly to manufacture, are subject to strict supply chain and storage constraints, and often require invasive administration routes. Engineered microbes that secrete bioactive products directly within the microbiome milieu may mitigate these challenges. Here, we describe a cell microfactory platform based on the probiotic yeast Saccharomyces boulardii for the production of nanobody biologics in the gastrointestinal (GI) tract. High-level secretion of nanobodies by S. boulardii was achieved by optimizing promoters, secretion signals and antibody formats. In mice, oral gavage of S. boulardii allowed efficient and transient colonization of the colonic compartment, and in situ production of a therapeutic nanobody directed against tumor necrosis factor (TNF). In a mouse model of chemical-induced colitis, GI-delivery of anti-murine TNF nanobody via live S. boulardii improved both survival and disease severity without causing overt perturbation of microbiome composition. These results position S. boulardii as a synthetic biotic platform for the in situ production and delivery of protein-based therapeutics to the GI tract.

Indexed as

Drug Delivery SystemsGastrointestinal TractInflammationSaccharomyces boulardiiSingle-Domain AntibodiesAnimalsColitisDisease Models, AnimalMice, Inbred C57BLTumor Necrosis Factor-alphaSingle-Domain AntibodiesTumor Necrosis Factor-alphaInflammatory bowel diseaseSaccharomyces boulardiiSynthetic bioticTNFVHH nanobody

Identifiers

PMID41800924
PMCPMC13035066

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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.