Evidence map›Paper›PMID 38017556›Full record

ArticleArthritis research & therapy2023

Characterization of human placenta-derived exosome (pExo) as a potential osteoarthritis disease modifying therapeutic.

Chenfei Huang, Yuechao Zhao, Shengchen Lin, Lin Li, Xuan Guo, Sebastian Yumiseba, Jeng-Dar Yang, Robert Hariri, Qian Ye, Shuyang He and 1 more

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

11 authors.

Chenfei HuangCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Yuechao ZhaoCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA. Yuechao.zhao@celularity.com.
Shengchen LinCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Lin LiCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Xuan GuoCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Sebastian YumisebaCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Jeng-Dar YangCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Robert HaririCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Qian YeCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Shuyang HeCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.
Adrian KilcoyneCelularity Inc., 170 Park Avenue, Florham Park, NJ, 07932, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHuman placenta-derived exosomes (pExo) were generated, characterized, and evaluated as a therapeutic candidate for the treatment of osteoarthritis (OA).

methodspExo was generated from full-term human placenta tissues by sequential centrifugation, purification, and sterile filtration. Upon analysis of particle size, cytokine composition, and exosome marker expression, pExo was further tested in cell-based assays to examine its effects on human chondrocytes. In vivo therapeutic efficacies were evaluated in a medial meniscal tear/medial collateral ligament tear (MCLT + MMT) rat model, in which animals received pExo injections intraarticularly and weight bearing tests during in-life stage while histopathology and immunohistochemistry were performed as terminal endpoints.

resultspExo displayed typical particle size, expressed maker proteins of exosome, and contained proteins with pro-proliferative, pro-anabolic, anti-catabolic, or anti-inflammatory activities. In vitro, pExo promoted chondrocyte migration and proliferation dose-dependently, which may involve its activation of cell growth-related signaling pathways. Expression of inflammatory and catabolic genes induced in a cellular OA model was significantly suppressed by pExo. In the rat OA model, pExo alleviated pain burden, restored cartilage degeneration, and downregulated expressions of pro-inflammatory, catabolic, or apoptotic proteins in a dose-dependent manner.

conclusionsOur study demonstrates that pExo has multiple potential therapeutic effects including symptom control and disease modifying characteristics. This may make it an attractive candidate for further development as an anti-OA therapeutic.

Indexed as

Cartilage, ArticularExosomesOsteoarthritisAnimalsAnti-Inflammatory AgentsChondrocytesHumansRatsAnti-Inflammatory AgentsExosomeOsteoarthritisPlacentaTherapeutic

Identifiers

PMID38017556
PMCPMC10683254

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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.