Evidence map›Paper›PMID 33394188›Full record

ArticleInflammation2021

High-Density-Immune-Complex Regulatory Macrophages Promote Recovery of Experimental Colitis in Mice.

Tamara Cristina Moreira Lopes, Gregório Guilherme Almeida, Izabela Aparecida Souza, Diego Costa Borges, Wanderson Geraldo de Lima, Pedro Henrique Dias Moura Prazeres, Alexander Birbrair, Rosa Maria Esteves Arantes, David M Mosser, Ricardo Goncalves

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  6. Article
  7. [The regulatory role and related mechanisms of macrophages in wound healing].Zhonghua shao shang yu chuang mian xiu fu za zhi · 2023
    Article
  8. Review
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.

Tamara Cristina Moreira LopesDepartamento de Patologia Geral-Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0002-5507-1602
Gregório Guilherme AlmeidaInstituto René Rachou-Fundação Oswaldo Cruz, MG, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0003-1108-1160
Izabela Aparecida SouzaDepartamento de Patologia Geral-Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0001-5890-6022
Diego Costa BorgesDepartamento de Bioquímica e Imunologia-Instituto de Ciências Biológicas, UFMG, Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0002-9680-6986
Wanderson Geraldo de LimaDepartamento de Ciências Biológicas-Instituto de Ciências Biológicas e Exatas, Universidade Federal de Ouro Preto (UFOP), Ouro Preto, MG, Brazil.ORCID https://orcid.org/0000-0001-9844-3472
Pedro Henrique Dias Moura PrazeresDepartamento de Patologia Geral-Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0002-1933-3230
Alexander BirbrairDepartamento de Patologia Geral-Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0003-1015-2561
Rosa Maria Esteves ArantesDepartamento de Patologia Geral-Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0003-1428-9717
David M MosserLaboratory of Macrophage and Host Defense - Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, USA.ORCID https://orcid.org/0000-0002-9503-4187
Ricardo GoncalvesDepartamento de Patologia Geral-Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil. ricardogoncalves2007@gmail.com.ORCID https://orcid.org/0000-0002-1127-4483
Universidade Federal de Minas Gerais · BRFundação Oswaldo Cruz · BRUniversidade Federal de Ouro Preto · BRUniversity of Maryland, College Park · US

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior schoolarshipFundação de Amparo à Pesquisa do Estado de Minas Gerais RED-00570-16
6 · The paper itself

Abstract

Macrophages not only play a fundamental role in the pathogenesis of inflammatory bowel disease (IBD), but they also play a major role in preserving intestinal homeostasis. In this work, we evaluated the role of macrophages in IBD and investigated whether the functional reprogramming of macrophages to a very specific phenotype could decrease disease pathogenesis. Thus, macrophages were stimulated in the presence of high-density immune complexes which strongly upregulate their production of IL-10 and downregulate pro-inflammatory cytokines. The transfer of these high-density-immune-complex regulatory macrophages into mice with colitis was examined as a potential therapy proposal to control the disease. Animals subjected to colitis induction received these high-density-immune-complex regulatory macrophages, and then the Disease Activity Index (DAI), and macroscopic and microscopic lesions were measured. The treated group showed a dramatic improvement in all parameters analyzed, with no difference with the control group. The colon was macroscopically normal in appearance and size, and microscopically colon architecture was preserved. The immunofluorescence migration assay showed that these cells migrated to the inflamed intestine, being able to locally produce the cytokine IL-10, which could explain the dramatic improvement in the clinical and pathological condition of the animals. Thus, our results demonstrate that the polarization of macrophages to a high IL-10 producer profile after stimulation with high-density immune complexes was decisive in controlling experimental colitis, and that macrophages are a potential therapeutic target to be explored in the control of colitis.

Indexed as

Adoptive TransferAnimalsAntigen-Antibody ComplexCells, CulturedColitisColonDextran SulfateDisease Models, AnimalInterleukin-10LipopolysaccharidesMacrophage ActivationMacrophagesMaleMiceMice, Inbred C57BLPhenotypeAntigen-Antibody ComplexDextran SulfateIL10 protein, mouseInterleukin-10LipopolysaccharidesIL-10inflammatory bowel diseasesmacrophagesulcerative colitis

Identifiers

PMID33394188
OpenAlexW3119662331

What OpenQuestion holds

Textmetadata
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.