Evidence map›Paper›PMID 35830711›Full record

ReviewCell biology international2022

siRNA-based nanotherapeutics as emerging modalities for immune-mediated diseases: A preliminary review.

Saman Sargazi, Rabia Arshad, Reza Ghamari, Abbas Rahdar, Ali Bakhshi, Sonia Fathi Karkan, Narges Ajalli, Muhammad Bilal, Ana M Díez-Pascual

Open access · greenAbstract readReview
In one paragraph

Review in Cell biology international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  5. Article
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  11. Nanomedicine for Cancer and Autoimmune Immunotherapy.International journal of molecular sciences · 2025
    Review
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  16. Article
  17. Current gene therapy · 2025
    Article
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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

9 authors at 9 institutions in 4 countries.

Saman SargaziCellular and Molecular Research Center, Research Institute of Cellular and Molecular Sciences in Infectious Diseases, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID http://orcid.org/0000-0002-2255-5977
Rabia ArshadDepartment of Pharmacy, Quaid-i-Azam University Islamabad, Islamabad, Pakistan.
Reza GhamariDepartment of Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.
Abbas RahdarDepartment of Physics, University of Zabol, Zabol, Iran.
Ali BakhshiSchool of Physics, Institute for Research in Fundamental Sciences (IPM), Tehran, Iran.ORCID http://orcid.org/0000-0001-9825-0806
Sonia Fathi KarkanStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Narges AjalliDepartment of Chemical Engineering, Faculty of Engineering, University of Tehran, Tehran, Iran.
Muhammad BilalSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huaian, China.
Ana M Díez-PascualUniversidad de Alcalá, Facultad de Ciencias, Departamento de Quimica Analítica, Química Física e Ingeniería Química, Ctra. Madrid-Barcelona, Alcalá de Henares, Madrid, Spain.ORCID http://orcid.org/0000-0001-7405-2354
Huaiyin Institute of Technology · CNInstitute for Research in Fundamental Sciences · IRNational Institute of Genetic Engineering and Biotechnology · IRQuaid-i-Azam University · PKTabriz University of Medical Sciences · IRUniversidad de Alcalá · ESUniversity of Tehran · IRZabol University · IRZahedan University of Medical Sciences · IR

Funding

Comunidad de Madrid EPU-INV/2020/012
6 · The paper itself

Abstract

Immune-mediated diseases (IMDs) are chronic conditions that have an immune-mediated etiology. Clinically, these diseases appear to be unrelated, but pathogenic pathways have been shown to connect them. While inflammation is a common occurrence in the body, it may either stimulate a favorable immune response to protect against harmful signals or cause illness by damaging cells and tissues. Nanomedicine has tremendous promise for regulating inflammation and treating IMIDs. Various nanoparticles coated with nanotherapeutics have been recently fabricated for effective targeted delivery to inflammatory tissues. RNA interference (RNAi) offers a tremendous genetic approach, particularly if traditional treatments are ineffective against IMDs. In cells, several signaling pathways can be suppressed by using RNAi, which blocks the expression of particular messenger RNAs. Using this molecular approach, the undesirable effects of anti-inflammatory medications can be reduced. Still, there are many problems with using short-interfering RNAs (siRNAs) to treat IMDs, including poor localization of the siRNAs in target tissues, unstable gene expression, and quick removal from the blood. Nanotherapeutics have been widely used in designing siRNA-based carriers because of the restricted therapy options for IMIDs. In this review, we have discussed recent trends in the fabrication of siRNA nanodelivery systems, including lipid-based siRNA nanocarriers, liposomes, and cationic lipids, stable nucleic acid-lipid particles, polymeric-based siRNA nanocarriers, polyethylenimine (PEI)-based nanosystems, chitosan-based nanoformulations, inorganic material-based siRNA nanocarriers, and hybrid-based delivery systems. We have also introduced novel siRNA-based nanocarriers to control IMIDs, such as pulmonary inflammation, psoriasis, inflammatory bowel disease, ulcerative colitis, rheumatoid arthritis, etc. This study will pave the way for new avenues of research into the diagnosis and treatment of IMDs.

Indexed as

NanomedicineNanoparticlesHumansInflammationLipidsRNA InterferenceRNA, Small InterferingLipidsRNA, Small Interferingautoimmunitydrug deliveryinflammationnanotechnologynanotherapeuticssiRNA

Identifiers

PMID35830711
PMCPMC9543380
OpenAlexW4285392577

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.