Evidence map›Paper›PMID 23691924›Full record

ArticleImmunology2013

Carbon monoxide exposure improves immune function in lupus-prone mice.

Juan P Mackern-Oberti, Carolina Llanos, Leandro J Carreño, Sebastián A Riquelme, Sergio H Jacobelli, Ignacio Anegon, Alexis M Kalergis

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Contribution of Dysregulated DNA Methylation to Autoimmunity.International journal of molecular sciences · 2021
    Review
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  7. Article
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  15. Article
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  17. Article
  18. Review
  19. Heme Oxygenase-1 in Kidney Health and Disease.Antioxidants & redox signaling · 2016
    Review
  20. 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

7 authors at 2 institutions in 2 countries.

Juan P Mackern-ObertiMillennium Institute on Immunology and Immunotherapy, Pontificia Universidad Católica de Chile, Santiago, Chile.
Carolina Llanos
Leandro J Carreño
Sebastián A Riquelme
Sergio H Jacobelli
Ignacio Anegon
Alexis M Kalergis
Millennium Institute on Immunology and Immunotherapy · CLInstitut de Transplantation Urologie en Nephrologie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by multiple alterations affecting the normal function of immune cells, such as lymphocytes, dendritic cells (DCs) and monocytes. Although the understanding of autoimmunity has significantly increased, the breakthrough in effective therapies has been modest, making necessary the development of new therapeutic strategies. Here we propose that a new potential target for therapy is haem oxygenase-1 (HO-1), an enzyme that catalyses the degradation of the haem group into biliverdin, carbon monoxide (CO) and Fe(2+) . These products exhibit immunosuppressive and anti-inflammatory effects, which can contribute to improving tolerance during organ transplantation. Because HO-1 is highly expressed by immune cells involved in SLE pathogenesis, such as monocytes and DCs, we evaluated whether induction of HO-1 expression or the administration of CO could ameliorate disease in the FcγRIIb knockout (KO) mouse model for SLE. We found that CO administration decreased the expansion of CD11b(+) cells, prevented the decline of regulatory T cells and reduced anti-histone antibodies observed in untreated FcγRIIb KO mice. Furthermore, CO-treated animals and HO-1 induction showed less kidney damage compared with untreated mice. These data suggest that HO-1 modulation and CO administration can ameliorate autoimmunity and prevent the lupus symptoms shown by FcγRIIb KO mice, highlighting HO-1 as a potential new target for autoimmune therapy.

Indexed as

AnimalsAutoimmunityCarbon MonoxideCD11b AntigenDisease Models, AnimalEnzyme InductionFemaleHeme Oxygenase-1KidneyLupus Erythematosus, SystemicMaleMembrane ProteinsMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutCarbon MonoxideCD11b AntigenFcgr2b protein, mouseHeme Oxygenase-1Hmox1 protein, mouseMembrane ProteinsReceptors, IgGcarbon monoxidehaem oxygenase-1systemic lupus erythematosus

Identifiers

PMID23691924
PMCPMC3809712
OpenAlexW2031170043

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.