Evidence map›Paper›PMID 41869412›Full record

ReviewInternational journal of nanomedicine2026

How Effective are Nanotechnology-Based Therapeutics to Treat Autoimmune Diseases.

Muna Barakat, Juhaina M Abu Ershaid, Lujain F Alzaghari, Shaymaa B Abdulrazzaq, Daniah Raad, Eliza Hasen, Raja'a A Al-Qudah, Dinesh Kumar Chellappan, Tamara Athamneh, Mohammad A A Al-Najjar and 1 more

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

11 authors.

Muna BarakatDepartment of Clinical Pharmacy and Therapeutics, Faculty of Pharmacy, Applied Science Private University, Amman, 11937, Jordan.ORCID 0000-0002-7966-1172
Juhaina M Abu ErshaidDepartment of Applied Pharmaceutical Sciences and Clinical Pharmacy, Faculty of Pharmacy, Isra University, Amman, 11622, Jordan.ORCID 0000-0001-8183-1532
Lujain F AlzaghariDepartment of Clinical Pharmacy and Therapeutics, Faculty of Pharmacy, Applied Science Private University, Amman, 11937, Jordan.ORCID 0009-0005-2493-0100
Shaymaa B AbdulrazzaqChemistry Interdisciplinary Project (CHIP), School of Science and Technology, University of Camerino, Via Madonna delle Carceri, Camerino, 62032, Italy.
Daniah RaadDepartment of Clinical Pharmacy and Therapeutics, Faculty of Pharmacy, Applied Science Private University, Amman, 11937, Jordan.
Eliza HasenKing Fahad Hospital, Al Hofuf, Eastern Province, Saudi Arabia.
Raja'a A Al-QudahDepartment of Clinical Pharmacy and Therapeutics, Faculty of Pharmacy, Applied Science Private University, Amman, 11937, Jordan.
Dinesh Kumar ChellappanDepartment of Life Sciences, School of Pharmacy, International Medical University, Bukit Jalil, Kuala Lumpur, 57000, Malaysia.ORCID 0000-0001-5567-6663
Tamara AthamnehInstitute of Nanotechnology, Jordan University of Science and Technology, Irbid, 22110, Jordan.
Mohammad A A Al-NajjarDepartment of Pharmaceutical Sciences and Pharmaceutics, Faculty of Pharmacy, Applied Science Private University, Amman, 11937, Jordan.
Akram AshamesDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, Ajman University, Ajman, United Arab Emirates.ORCID 0000-0003-3124-8802

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune diseases are chronic, debilitating conditions caused by the immune system mistakenly attacking healthy tissues. Conventional treatments mainly involve broad immunosuppression, which is associated with significant side effects, limited specificity, and suboptimal long-term outcomes. For instance, continuing to take corticosteroids can result in a number of serious dose-linked toxicities, such as osteoporosis, hypertension, and a markedly increased susceptibility to infection, whereas methotrexate, even at therapeutic doses, can still cause liver damage and bone marrow suppression. This review aims to explore recent advances in nanotechnology-based therapies for autoimmune diseases, focusing on their mechanisms, therapeutic applications, and potential for clinical translation. A comprehensive review of peer-reviewed literature was conducted to examine various nanotechnology platforms, including drug-loaded nanoparticles, antigen-specific nanomedicines, RNA interference (siRNA), CRISPR-enabled systems, and stimuli-responsive nanocarriers. For instance, methotrexate-loaded polymeric nanoparticles dramatically decreased arthritis severity in preclinical rheumatoid arthritis rodents, whereas PLGA nanoparticles containing gluten protein induced immunological tolerance in a clinical study for celiac disease. Nanomedicine offers several advantages over traditional therapies, including targeted drug delivery, enhanced bioavailability, reduced systemic toxicity, and the potential to induce immune tolerance. Notable innovations include biodegradable polymeric nanoparticles, liposomes, micelles, exosome-mimetic nanoparticles, and magnetic nanomaterials. Emerging technologies, such as CRISPR-Cas9 and RNAi, delivered via nanoparticles, are advancing immune modulation in autoimmune models. Despite promising outcomes, several barriers remain, including concerns about toxicity, scale-up manufacturing issues, and regulatory challenges. Nanotechnology is redefining autoimmune disease therapy by shifting from non-specific immunosuppression to precision-targeted approaches. Future progress lies in integrating nanomedicine with personalized medicine to tailor treatments based on individual immune profiles. Continued interdisciplinary collaboration and regulatory alignment are essential to translating these innovations into clinical practice.

Indexed as

Autoimmune DiseasesNanomedicineAnimalsDrug Delivery SystemsHumansNanoparticlesNanotechnologyRNA, Small InterferingRNA, Small Interferingautoimmune diseasesImmunomodulationnanomedicineRNAiRNA interferencetargeted drug delivery

Identifiers

PMID41869412
PMCPMC13003824

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.