Evidence map›Paper›PMID 37629159›Full record

Trial reportInternational journal of molecular sciences2023

A Novel Multi-Component Formulation Reduces Inflammation In Vitro and Clinically Lessens the Symptoms of Chronic Eczematous Skin.

Jihee Kim, Eunjoong Jung, Wonmi Yang, Chun-Kang Kim, Serpen Durnaoglu, In-Rok Oh, Chan-Wha Kim, Anthony J Sinskey, Martin C Mihm, Ju Hee Lee

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Article
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

10 authors at 4 institutions in 2 countries.

Jihee KimDepartment of Dermatology & Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.ORCID 0000-0002-0047-5941
Eunjoong JungBiocoz Global Korea, R & D Center, Seoul 03181, Republic of Korea.ORCID 0000-0002-8790-4066
Wonmi YangBiocoz Global Korea, R & D Center, Seoul 03181, Republic of Korea.
Chun-Kang KimBiocoz Global Korea, R & D Center, Seoul 03181, Republic of Korea.
Serpen DurnaogluBiocoz Global Korea, R & D Center, Seoul 03181, Republic of Korea.ORCID 0000-0001-6902-2492
In-Rok OhBiocoz Global Korea, R & D Center, Seoul 03181, Republic of Korea.ORCID 0000-0001-8177-7556
Chan-Wha KimBiocoz Global Korea, R & D Center, Seoul 03181, Republic of Korea.
Anthony J SinskeyDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.ORCID 0000-0002-1015-1270
Martin C MihmDepartment of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Ju Hee LeeDepartment of Dermatology & Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Bio-Medical Science (South Korea) · KRYonsei University · KRBrigham and Women's Hospital · USMassachusetts Institute of Technology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term treatments for inflammatory skin diseases like atopic dermatitis or eczema can cause adverse effects. Super Protein Multifunction (SPM) was investigated as a potential treatment for managing skin inflammation by monitoring the expression of pro-inflammatory cytokines induced using LPS and poly(I:C)/TNFα in HaCaT keratinocytes and Hs27 fibroblasts as measured via RT-PCR. SPM solution was also assessed for its effect on cytokine release, measured using ELISA, in a UVB-irradiated 3D human skin model. To evaluate the efficiency of SPM, 20 patients with mild eczematous skin were randomized to receive SPM or vehicle twice a day for three weeks in a double-blind controlled trial. In vitro studies showed SPM inhibited inflammation-induced IL-1β, IL-6, IL-33, IL-1α, TSLP, and TNFα expression or release. In the clinical study, the SPM group showed significant improvements in the IGA, PA, and DLQI scores compared to the vehicle group. Neither group showed significant differences in VAS (pruritus). Histological analysis showed reduced stratum corneum thickness and inflammatory cell infiltration. The results suggest that SPM may reduce inflammation in individuals with chronic eczematous skin.

Indexed as

EczemaTumor Necrosis Factor-alphaCytokinesExcipientsHumansInflammationPruritusSkinCytokinesExcipientsTumor Necrosis Factor-alpha3D skin modelanti-inflammationchronic eczemacytokinekeratinocytesskin

Identifiers

PMID37629159
PMCPMC10454735
OpenAlexW4386030029

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.