Evidence map›Paper›PMID 41329324›Full record

ReviewBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2026

Recombinant Molecules as a New Frontier in Mucositis Therapy.

Luís Cláudio Lima de Jesus, Rhayane Cristina Viegas Santos, Vasco Azevedo

Abstract readReview
PubMed Publisher
In one paragraph

Review in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 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

3 authors.

Luís Cláudio Lima de JesusDepartment of Genetics, Ecology and Evolution, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil. luiislimma@gmail.com.ORCID http://orcid.org/0000-0001-7708-3033
Rhayane Cristina Viegas SantosDepartment of Genetics, Ecology and Evolution, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Vasco AzevedoDepartment of Genetics, Ecology and Evolution, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil. vasco@icb.ufmg.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucositis significantly impairs patients' quality of life, and despite its clinical importance and the availability of symptomatic treatments, no gold-standard therapeutic protocol has been established. Recent advances in biotechnology and molecular biology have enabled the development of genetically engineered probiotic strains capable of producing or delivering therapeutic molecules directly to inflamed mucosal sites. Although several recombinant biotherapeutic bacteria have advanced to clinical evaluation, most have not yet reproduced the efficacy observed in preclinical models, and no products have yet been commercially approved for human use. This is the first review to comprehensively outline the recombinant molecules as an innovative biotherapeutic option for mucosal inflammation induced by chemoradiotherapy. In this review, we describe how genetically modified bacteria function as living drug delivery platforms, focusing on their ability to produce or deliver recombinant molecules, including antimicrobial peptides, antioxidant enzymes, growth factors, and interleukin receptor antagonists, for mucositis therapy. We further discuss key limitations, including biosafety, control of gene expression, and gut protection levels, while outlining future challenges.

Indexed as

MucositisRecombinant ProteinsAnimalsAntimicrobial PeptidesChemoradiotherapyDrug Delivery SystemsHumansProbioticsAntimicrobial PeptidesRecombinant Proteins

Identifiers

What Socratic holds

Textmetadata
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.