Evidence map›Paper›PMID 36686276›Full record

ArticleJournal of inflammation research2023

Anti-Inflammatory Effects of the 35kDa Hyaluronic Acid Fragment (B-HA/HA35).

XiaoXiao Jia, Ming Shi, Qifei Wang, Jessica Hui, Joshua Hui Shofaro, Ryenchindorj Erkhembayar, Mizhou Hui, Chenzhe Gao, Munkh-Amgalan Gantumur

3 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Journal of inflammation research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.8field-weighted citation impact, top 5% 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.

NCT05756595 nacompletednot on this map

A Preliminary Clinical Study of Freshly Manufactured 35kDa Hyaluronan Fragment in the Treatment of Herpes Zoster Pain and Shoulder, Neck, Back and Temporal Pain

TypeinterventionalSponsorDove Medical Press LtdRan2020 to 2023Enrolled36ConditionsShoulder Pain, Neck Pain, Back Pain, Temporal PainArmsHA35(L20200708MP07707, Ministry of Health, Mongolia) was freshly manufactured by mixing hyaluronidase PH20 injectable solution (H31022111) and high-molecular-weight HA injectable solution (H20174089)
NCT05764226 nacompletednot on this map

A Clinical Study of Freshly Manufactured 35kDa Hyaluronan Fragment HA35 for Treatment of Chronic Wounds

TypeinterventionalSponsorNakhia Impex LLCRan2020 to 2023Enrolled20ConditionsChronic WoundsArmsHA35(L20200708MP07707, Ministry of Health, Mongolia)was freshly manufactured by mixing hyaluronidase PH20 injectable solution (H31022111) and high-molecular-weight HA injectable solution (H20174089)
NCT05765513 nacompletednot on this map

Intra-pocket Injection of a Freshly Manufactured 35 kDa Hyaluronan Fragment HA35 Reduces the Gingival Discomfort as Well as Gingival Redness and Bleeding of Patients With Periodontitis: A Clinical Study

TypeinterventionalSponsorDove Medical Press LtdRan2023 to 2023Enrolled20ConditionsPeriodontitisArmsHA35(L20200708MP07707, Ministry of Health, Mongolia) was freshly manufactured by mixing hyaluronidase PH20 injectable solution (H31022111) and high-molecular-weight HA injectable solution (H20174089)
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  4. Review
  5. Histopathological characterization of skin and muscle lesions induced by lionfish (The journal of venomous animals and toxins including tropical diseases · 2025
    Article
  6. 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 5 institutions in 3 countries.

XiaoXiao Jia *College of Life Science, Northeast Agricultural University, Harbin, People's Republic of China.
Ming Shi *School of Life Science and Technology, Harbin Institute of Technology, Harbin, People's Republic of China.ORCID 0000-0003-0527-0061
Qifei WangCollege of Life Science, Northeast Agricultural University, Harbin, People's Republic of China.
Jessica HuiCenter for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, USA.
Joshua Hui ShofaroCollege of Life Science, Northeast Agricultural University, Harbin, People's Republic of China.
Ryenchindorj ErkhembayarDepartment of International Cyber Education, Graduate School, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia.
Mizhou HuiCollege of Life Science, Northeast Agricultural University, Harbin, People's Republic of China.
Chenzhe GaoCollege of Life Science, Northeast Agricultural University, Harbin, People's Republic of China.
Munkh-Amgalan GantumurCollege of Life Science, Northeast Agricultural University, Harbin, People's Republic of China.
Qingdao Agricultural University · CNNortheast Agricultural University · CNHarbin Institute of Technology · CNMongolian National University · MNStanford University · US

Funding

CENTER FOR GAMMA RAY IMAGINGP41EB002035 · NIBIB · UNIVERSITY OF ARIZONA · PI BARRETT, HARRISON H, FURENLID, LARS R · 2003 to 2018
$17.7M
NIBIB NIH HHS P41 EB002035
6 · The paper itself

Abstract

Background: Hyaluronic acid (HA) and HA fragments interact with a variety of human body receptors and are involved in the regulation of various physiological functions and leukocyte trafficking in the body. Accordingly, the development of an injectable HA fragment with good tissue permeability, the identification of its indications, and molecular mechanisms are of great significance for its clinical application. The previous studies showed that the clinical effects of injectable 35kDa B-HA result from B-HA binding to multiple receptors in different cells, tissues, and organs. This study lays the foundation for further studies on the comprehensive clinical effects of injectable B-HA. Methods: We elaborated on the production process, bioactivity assay, efficacy analyses, and safety evaluation of an injectable novel HA fragment with an average molecular weight of 35 kDa (35 kDa B-HA), produced by recombinant human hyaluronidase PH20 digestion. Results: The results showed that 35 kDa B-HA induced human erythrocyte aggregation (rouleaux formation) and accelerated erythrocyte sedimentation rates through the CD44 receptor. B-HA application and injection treatment significantly promoted the removal of mononuclear cells from the site of inflammation and into the lymphatic circulation. At a low concentration, 35 kDa B-HA inhibited production of reactive oxygen species and tumor necrosis factor by neutrophils; at a higher concentration, 35 kDa B-HA promoted the migration of monocytes. Furthermore, 35 kDa B-HA significantly inhibited the migration of neutrophils with or without lipopolysaccharide treatment, suggesting that in local tissues, higher concentrations of 35 kDa B-HA have antiinflammatory effects. After Conclusion: This study demonstrated that the HA fragment B-HA has good tissue permeability and antiinflammatory effects, laying a theoretical foundation for further clinical studies.

Indexed as

35kDa hyaluronic acid fragmentB-HA/HA35hyaluronic acidinflammationinflammatory cellsinjection safetymolecular weightreactive oxygen species

Identifiers

PMID36686276
PMCPMC9846287
OpenAlexW4315782750

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.