Evidence map›Paper›PMID 26322981›Full record

ArticlePloS one2015

Human Tubal-Derived Mesenchymal Stromal Cells Associated with Low Level Laser Therapy Significantly Reduces Cigarette Smoke-Induced COPD in C57BL/6 mice.

Jean Pierre Schatzmann Peron, Auriléia Aparecida de Brito, Mayra Pelatti, Wesley Nogueira Brandão, Luana Beatriz Vitoretti, Flávia Regina Greiffo, Elaine Cristina da Silveira, Manuel Carneiro Oliveira-Junior, Mariangela Maluf, Lucila Evangelista and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.9field-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.

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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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  16. Mesenchymal stromal cell therapy in COPD: from bench to bedside.International journal of chronic obstructive pulmonary disease · 2017
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Jean Pierre Schatzmann PeronNeuroimmune Interactions Laboratory, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, SP, Brazil.
Auriléia Aparecida de BritoLaboratory of Pulmonary and Exercise Immunology-LABPEI, Nove de Julho University (UNINOVE), São Paulo, SP, Brazil.
Mayra PelattiDivision of Human Genome Research Center, Biosciences Institute, University of São Paulo, São Paulo, SP, Brazil.
Wesley Nogueira BrandãoNeuroimmune Interactions Laboratory, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, SP, Brazil.
Luana Beatriz VitorettiLaboratory of Pulmonary and Exercise Immunology-LABPEI, Nove de Julho University (UNINOVE), São Paulo, SP, Brazil.
Flávia Regina GreiffoLaboratory of Pulmonary and Exercise Immunology-LABPEI, Nove de Julho University (UNINOVE), São Paulo, SP, Brazil.
Elaine Cristina da SilveiraLaboratory of Pulmonary and Exercise Immunology-LABPEI, Nove de Julho University (UNINOVE), São Paulo, SP, Brazil.
Manuel Carneiro Oliveira-JuniorDivision of Human Genome Research Center, Biosciences Institute, University of São Paulo, São Paulo, SP, Brazil.
Mariangela MalufCEERH-Specialized Center for Human Reproduction, Division of Reproductive Medicine, São Paulo, SP, Brazil.
Lucila EvangelistaDivision of Reproductive Medicine-Célula Mater, São Paulo, SP, Brazil.
Silvio HalpernDivision of Reproductive Medicine-Célula Mater, São Paulo, SP, Brazil.
Marcelo Gil NisenbaumDivision of Reproductive Medicine-Célula Mater, São Paulo, SP, Brazil.
Paulo PerinCEERH-Specialized Center for Human Reproduction, Division of Reproductive Medicine, São Paulo, SP, Brazil.
Carlos Eduardo CzeresniaDivision of Reproductive Medicine-Célula Mater, São Paulo, SP, Brazil.
Niels Olsen Saraiva CâmaraLaboratory of Transplantation Immunobiology, Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Flávio AimbireDepartment of Science and Technology, Federal University of São Paulo, São José dos Campos, SP, Brazil.
Rodolfo de Paula VieiraDivision of Human Genome Research Center, Biosciences Institute, University of São Paulo, São Paulo, SP, Brazil.
Mayana ZatzLaboratory of Pulmonary and Exercise Immunology-LABPEI, Nove de Julho University (UNINOVE), São Paulo, SP, Brazil.
Ana Paula Ligeiro de OliveiraDivision of Human Genome Research Center, Biosciences Institute, University of São Paulo, São Paulo, SP, Brazil.
Universidade de São Paulo · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cigarette smoke-induced chronic obstructive pulmonary disease is a very debilitating disease, with a very high prevalence worldwide, which results in a expressive economic and social burden. Therefore, new therapeutic approaches to treat these patients are of unquestionable relevance. The use of mesenchymal stromal cells (MSCs) is an innovative and yet accessible approach for pulmonary acute and chronic diseases, mainly due to its important immunoregulatory, anti-fibrogenic, anti-apoptotic and pro-angiogenic. Besides, the use of adjuvant therapies, whose aim is to boost or synergize with their function should be tested. Low level laser (LLL) therapy is a relatively new and promising approach, with very low cost, no invasiveness and no side effects. Here, we aimed to study the effectiveness of human tube derived MSCs (htMSCs) cell therapy associated with a 30mW/3J-660 nm LLL irradiation in experimental cigarette smoke-induced chronic obstructive pulmonary disease. Thus, C57BL/6 mice were exposed to cigarette smoke for 75 days (twice a day) and all experiments were performed on day 76. Experimental groups receive htMSCS either intraperitoneally or intranasally and/or LLL irradiation either alone or in association. We show that co-therapy greatly reduces lung inflammation, lowering the cellular infiltrate and pro-inflammatory cytokine secretion (IL-1β, IL-6, TNF-α and KC), which were followed by decreased mucus production, collagen accumulation and tissue damage. These findings seemed to be secondary to the reduction of both NF-κB and NF-AT activation in lung tissues with a concomitant increase in IL-10. In summary, our data suggests that the concomitant use of MSCs + LLLT may be a promising therapeutic approach for lung inflammatory diseases as COPD.

Indexed as

AdultAnimalsBronchoalveolar Lavage FluidCells, CulturedFemaleHumansInterleukin-1betaInterleukin-6Low-Level Light TherapyLungMesenchymal Stem CellsMiceMice, Inbred C57BLMiddle AgedNFATC Transcription FactorsNF-kappa BInterleukin-1betaInterleukin-6NFATC Transcription FactorsNF-kappa BSmokeTumor Necrosis Factor-alpha

Identifiers

PMID26322981
PMCPMC4554986
OpenAlexW1894130643

What OpenQuestion holds

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Registered trials

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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.