Evidence map›Paper›PMID 35740354›Full record

ReviewBiomedicines2022

Unbalanced IDO1/IDO2 Endothelial Expression and Skewed Keynurenine Pathway in the Pathogenesis of COVID-19 and Post-COVID-19 Pneumonia.

Marco Chilosi, Claudio Doglioni, Claudia Ravaglia, Guido Martignoni, Gian Luca Salvagno, Giovanni Pizzolo, Vincenzo Bronte, Venerino Poletti

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Kynurenine Pathway in Respiratory Diseases.International journal of tryptophan research : IJTR · 2024
    Review
  9. Article
  10. Article
  11. 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

8 authors at 6 institutions in 2 countries.

Marco ChilosiDepartment of Pathology, Pederzoli Hospital, 37019 Peschiera del Garda, Italy.
Claudio DoglioniDepartment of Pathology, San Raffaele Scientific Institute, 20132 Milan, Italy.ORCID 0000-0002-4969-5216
Claudia RavagliaDepartment of Diseases of the Thorax, Ospedale GB Morgagni, University of Bologna, 47121 Forlì, Italy.
Guido MartignoniDepartment of Pathology, Pederzoli Hospital, 37019 Peschiera del Garda, Italy.
Gian Luca SalvagnoSection of Clinical Biochemistry, University of Verona, 37134 Verona, Italy.
Giovanni PizzoloDepartment of Medicine, Section of Hematology, University of Verona, 37134 Verona, Italy.
Vincenzo BronteIstituto Oncologico Veneto, IOV-IRCCS, 35100 Padova, Italy.
Venerino PolettiDepartment of Diseases of the Thorax, Ospedale GB Morgagni, University of Bologna, 47121 Forlì, Italy.
University of Verona · ITAarhus University Hospital · DKCasa di Cura Villa Garda · ITIstituto Oncologico Veneto · ITSan Raffaele University of Rome · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite intense investigation, the pathogenesis of COVID-19 and the newly defined long COVID-19 syndrome are not fully understood. Increasing evidence has been provided of metabolic alterations characterizing this group of disorders, with particular relevance of an activated tryptophan/kynurenine pathway as described in this review. Recent histological studies have documented that, in COVID-19 patients, indoleamine 2,3-dioxygenase (IDO) enzymes are differentially expressed in the pulmonary blood vessels, i.e., IDO1 prevails in early/mild pneumonia and in lung tissues from patients suffering from long COVID-19, whereas IDO2 is predominant in severe/fatal cases. We hypothesize that IDO1 is necessary for a correct control of the vascular tone of pulmonary vessels, and its deficiency in COVID-19 might be related to the syndrome's evolution toward vascular dysfunction. The complexity of this scenario is discussed in light of possible therapeutic manipulations of the tryptophan/kynurenine pathway in COVID-19 and post-acute COVID-19 syndromes.

Indexed as

COVID-19IDOPACSpost-acute COVID syndromeSARS-CoV-2tryptophan/kynurenine

Identifiers

PMID35740354
PMCPMC9220124
OpenAlexW4281646572

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.