Evidence map›Paper›PMID 36964609›Full record

ReviewJournal of nanobiotechnology2023

Combining nanotechnology with monoclonal antibody drugs for rheumatoid arthritis treatments.

Xiao-Kai Chi, Xiao-Ling Xu, Bang-Yao Chen, Jin Su, Yong-Zhong Du

Open access · goldFull text readReview
In one paragraph

Review in Journal of nanobiotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
7.6field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Xiao-Kai ChiCollege of Pharmacy, Jiamusi University, 258 Xuefu Road, Jiamusi, 154007, China.
Xiao-Ling XuShulan International Medical College, Zhejiang Shuren University), 8 Shuren Street, Hangzhou, 310015, China. ziyao1988@zju.edu.cn.
Bang-Yao ChenShulan International Medical College, Zhejiang Shuren University), 8 Shuren Street, Hangzhou, 310015, China.
Jin SuCollege of Pharmacy, Jiamusi University, 258 Xuefu Road, Jiamusi, 154007, China. sujin@jmsu.edu.cn.
Yong-Zhong DuInstitute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, 866 Yu-Hang-Tang Road, Hangzhou, 310058, China. duyongzhong@zju.edu.cn.
Jiamusi University · CNZhejiang Shuren University · CNZhejiang University · CN

Funding

National Natural Science Foundation of China 81874302university level scientific research project of Zhejiang Shuren University 2022R005
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a systemic immune disease characterized by synovial inflammation. Patients with RA commonly experience significant damage to their hand and foot joints, which can lead to joint deformities and even disability. Traditional treatments have several clinical drawbacks, including unclear pharmacological mechanisms and serious side effects. However, the emergence of antibody drugs offers a promising approach to overcome these limitations by specifically targeting interleukin-1 (IL-1), interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and other cytokines that are closely related to the onset of RA. This approach reduces the incidence of adverse effects and contributes to significant therapeutic outcomes. Furthermore, combining these antibody drugs with drug delivery nanosystems (DDSs) can improve their tissue accumulation and bioavailability.Herein, we provide a summary of the pathogenesis of RA, the available antibody drugs and DDSs that improve the efficacy of these drugs. However, several challenges need to be addressed in their clinical applications, including patient compliance, stability, immunogenicity, immunosupression, target and synergistic effects. We propose strategies to overcome these limitations. In summary, we are optimistic about the prospects of treating RA with antibody drugs, given their specific targeting mechanisms and the potential benefits of combining them with DDSs.

Indexed as

Antibodies, MonoclonalArthritis, RheumatoidCytokinesHumansInflammationPharmaceutical PreparationsTumor Necrosis Factor-alphaAntibodies, MonoclonalCytokinesPharmaceutical PreparationsTumor Necrosis Factor-alphaAntibody drugsDrug delivery nanosystemRheumatoid arthritis

Identifiers

PMID36964609
PMCPMC10039584
OpenAlexW4360941998

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read56
identifiers read1
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.