Evidence map›Paper›PMID 39378196›Full record

ArticlePloS one2024

Immunotherapeutic potential of collagen V oral administration in mBSA/CFA-induced arthritis.

Lizandre Keren Ramos da Silveira, Ana Paula P Velosa, Sergio Catanozi, Marco Aurélio A Pereira, Antonio Dos Santos Filho, Fabio Luiz N Marques, Daniele de Paula Faria, Caroline Cristiano Real, Sandra de M Fernezlian, Amanda Flores Yanke and 9 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Lizandre Keren Ramos da SilveiraDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.ORCID 0000-0002-5275-4045
Ana Paula P VelosaDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Sergio CatanoziLaboratorio de Lipides (LIM-10), Hospital das Clinicas (HCFMUSP) da Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, Brazil.
Marco Aurélio A PereiraDepartment of Surgery, School of Veterinary Medicine and Animal Science, University of Sao Paulo, Sao Paulo, Brazil.
Antonio Dos Santos FilhoDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Fabio Luiz N MarquesLaboratory of Nuclear Medicine (LIM 43), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Daniele de Paula FariaLaboratory of Nuclear Medicine (LIM 43), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Caroline Cristiano RealLaboratory of Nuclear Medicine (LIM 43), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Sandra de M FernezlianDepartment of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, São Paulo, Brazil.
Amanda Flores YankeDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Zelita Aparecida de J QueirozDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Vitória Elias ContiniDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Thays de Matos LoboDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Solange CarrascoDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Camila Machado BaldaviraDepartment of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, São Paulo, Brazil.
Cláudia Goldenstein-SchainbergDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.ORCID 0000-0003-3306-9699
Ricardo FullerDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Vera L CapelozziDepartment of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, São Paulo, Brazil.
Walcy R TeodoroDivision of Rheumatology, Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, SP, Brazil.ORCID 0000-0001-7559-4542

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We hypothesized that after synovial injury, collagen V (Col V) expose occult antigens, and Col V autoantibodies develop, indicating the loss of immune tolerance against this molecule, thus leading to damage to mesenchymal-derived cells as well as the extracellular matrix in experimental arthritis. Thus, the present study investigated the effects of oral administration of Col V on the synovium after the development of inflammation in mBSA/CFA-induced arthritis. After fourteen days of intraarticular administration of mBSA, 10 male Lewis rats were orally administered Col V (500 μg/300 μL) diluted in 0.01 N acetic acid (IA-Col V group). The arthritic group (IA group, n = 10) received only intraarticular mBSA. An intra-articular saline injection (20 μL) was given to the control group (CT-Col V, n = 5). IA group presented damaged synovia, the expansion of the extracellular matrix by cellular infiltrate, which was characterized by T and B lymphocytes, and fibroblastic infiltration. In contrast, after Col V oral immunotherapy IA-Col V group showed a significant reduction in synovial inflammation and intense expression of IL-10+ and FoxP3+ cells, in addition to a reduction in Col V and an increase in Col I in the synovia compared to those in the IA group. Furthermore, an increase in IL-10 production was detected after IA-Col V group spleen cell stimulation with Col V in vitro. PET imaging did not differ between the groups. The evaluation of oral treatment with Col V, after mBSA/CFA-induced arthritis in rats, protects against inflammation and reduces synovial tissue damage, through modulation of the synovial matrix, showing an immunotherapeutic potential in inhibiting synovitis.

Indexed as

Arthritis, ExperimentalCollagen Type VRats, Inbred LewSynovial MembraneAdministration, OralAnimalsForkhead Transcription FactorsFreund's AdjuvantImmunotherapyInterleukin-10MaleRatsSerum Albumin, BovineCollagen Type VForkhead Transcription FactorsFoxp3 protein, ratFreund's AdjuvantInterleukin-10methylated bovine serum albuminSerum Albumin, Bovine

Identifiers

PMID39378196
PMCPMC11460680

What Socratic 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 Socratic graph.