Evidence map›Paper›PMID 34715852›Full record

ReviewJournal of nanobiotechnology2021

How could nanobiotechnology improve treatment outcomes of anti-TNF-α therapy in inflammatory bowel disease? Current knowledge, future directions.

Piotr Eder, Aleksandra Zielińska, Jacek Karczewski, Agnieszka Dobrowolska, Ryszard Słomski, Eliana B Souto

Open access · goldAbstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
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

10 citing papers in PubMed, 25 citations in OpenAlex.

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  10. Interactions between Nanoparticles and Intestine.International journal of molecular sciences · 2022
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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

6 authors at 3 institutions in 2 countries.

Piotr Eder *Department of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego Street 49, 60-355, Poznan, Poland. piotreder@ump.edu.pl.ORCID http://orcid.org/0000-0001-9306-5038
Aleksandra Zielińska *Institute of Human Genetics, Polish Academy of Sciences, Strzeszyńska 32, 60-479, Poznan, Poland. aleksandra.zielinska@igcz.poznan.pl.ORCID http://orcid.org/0000-0003-2603-1377
Jacek KarczewskiDepartment of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego Street 49, 60-355, Poznan, Poland.
Agnieszka DobrowolskaDepartment of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego Street 49, 60-355, Poznan, Poland.
Ryszard SłomskiInstitute of Human Genetics, Polish Academy of Sciences, Strzeszyńska 32, 60-479, Poznan, Poland.
Eliana B SoutoCEB-Centre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal. eliana.souto@ceb.uminho.pt.ORCID http://orcid.org/0000-0002-9737-6017
Poznan University of Medical Sciences · PLInstitute of Human Genetics · PLUniversity of Minho · PT

Funding

Fundação para a Ciência e a Tecnologia UIDB/04469/2020Fundacja na rzecz Nauki Polskiej START 2021Narodowe Centrum Nauki 2020/04/X/ST5/00789
6 · The paper itself

Abstract

Despite significant advances in therapeutic possibilities for the treatment of inflammatory bowel disease (IBD) in recent years, there is still a big room for improvement. In particular, biological treatment can induce not only clinical remission but also mucosal healing of the gastrointestinal tract. Among these therapeutic molecules, anti-tumor necrosis factor-alpha (anti-TNF-α) antibodies were the first to revolutionize treatment algorithms in IBD. However, due to the parenteral route of administration and systemic mode of action, TNF-α blockers are characterised by high rates of immunogenicity-related loss of response and serious adverse events. Moreover, intravenous or subcutaneous therapy is not considered patient-friendly and requires occasional, direct contact with healthcare centres. To overcome these limitations, several attempts have been made to design oral pharmaceutical formulations of these molecules. It is hypothesized that oral anti-TNF-α antibodies therapy can directly provide a targeted and potent anti-inflammatory effect in the inflamed gastrointestinal tissues without significant systemic exposure, improving long-term treatment outcomes and safety. In this review, we discuss the current knowledge and future perspectives regarding different approaches made towards entering a new era of oral anti-TNF-α therapy, namely, the tailoring of biocompatible nanoparticles with anti-TNF-α antibodies for site-specific targeting to IBD. In particular, we discuss the latest concepts applying the achievements of nanotechnology-based drug design in this area.

Indexed as

Administration, OralAntibodies, MonoclonalColitisHumansImmunoglobulin GImmunotherapyInflammatory Bowel DiseasesLiposomesNanoparticlesTreatment OutcomeTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAntibodies, MonoclonalImmunoglobulin GLipid NanoparticlesLiposomesTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAnti-TNF-α antibodies therapyInflammatory bowel diseasesLipid nanoparticlesOral drug delivery

Identifiers

PMID34715852
PMCPMC8554748
OpenAlexW3210752631

What OpenQuestion 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 OpenQuestion graph.