Evidence map›Paper›PMID 36761174›Full record

ArticleFrontiers in immunology2022

Identification of autoimmune markers in pulmonary tuberculosis.

Anna Starshinova, Anna Malkova, Yulia Zinchenko, Igor Kudryavtsev, Maria Serebriakova, Tatiana Akisheva, Sergey Lapin, Aleksandra Mazing, Dmitry Kudlay, Anzhela Glushkova and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. 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

12 authors at 7 institutions in 2 countries.

Anna StarshinovaSt. Petersburg State University, St. Petersburg, Russia.
Anna MalkovaSt. Petersburg State University, St. Petersburg, Russia.
Yulia ZinchenkoSt. Petersburg State University, St. Petersburg, Russia.
Igor KudryavtsevDepartment of Immunology, Institution of Experimental Medicine, St. Petersburg, Russia.
Maria SerebriakovaDepartment of Immunology, Institution of Experimental Medicine, St. Petersburg, Russia.
Tatiana AkishevaDepartment of Immunology, Institution of Experimental Medicine, St. Petersburg, Russia.
Sergey LapinSt. Petersburg State Medical University, St. Petersburg, Russia.
Aleksandra MazingFirst Moscow State Medical University, Moscow, Russia.
Dmitry KudlayInstitute of Immunology, Moscow, Russia.
Anzhela GlushkovaZabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel.
Piotr YablonskiySt. Petersburg State University, St. Petersburg, Russia.
Yehuda ShoenfeldSt. Petersburg State University, St. Petersburg, Russia.
Institute of Experimental Medicine · RUSt Petersburg University · RUSheba Medical Center · ILSaint-Petersburg Research Institute of Phthisiopulmonology · RUSaint Petersburg State Pediatric Medical University · RUSechenov University · RUSt.Petersburg V.M.Bekhterev Psychoneurological Research Institute · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Pathogenesis of many autoimmune diseases is mainly promoted by poorly regulated and/or wrong targeted immune response to pathogens including Materials and methods: A prospective comparative study was performed in 2017 - 2019 with the inclusion of 46 patients with Tbc. The trigger factors and clinical manifestations, autoantibodies, peripheral blood B cell subsets were stained with fluorochrome-conjugated monoclonal antibodies. 40 healthy volunteers in the control group, were matched for age with no chronic diseases, contacts with TB patients and changes in their laboratory parameters. A statistical analysis was done with GraphPad Prism 6, Statistica 10 (Statsoft) and MedCalc - version 18.2.1 values. Results: There were no significant ASIA triggers in Tbc patients and control group. 21.1% of Tbc patients had a high level of a rheumatoid factor and in 47.4% complement system factor C3 was high; anti-MCV was detected in 60.7% of Tbc patients. Relative and absolute frequencies of "naïve" Bm1 cells and eBm5 were significantly decreased and activated pre-germinal-center Bm2' cells were significantly increased in Tbc patients. The CD24++CD38++ B cells were increased in Tbc vs control group (10.25% vs 5.42%), p < 0.001, and 19 cell/1μL (10; 290 vs 11 cell/1μL (6; 20), p = 0.029, respectively). The frequency of CXCR3+CCR4- Tfh1 cells was significantly lower in Tbc vs control one (26.52% vs. 31.00%, p = 0.004), while CXCR3-CCR4+ Tfh2 cells were increased in Tbc (20.31% vs. controls (16.56%, p = 0.030). The absolute numbers of Tfh1 cells were decreased in the Tbc vs. control (24 cell/1μL vs. 37 cell/1μL p = 0.005). Conclusion: The results of our study showed that the detection of a rheumatoid factor, the components of complement system and anti-MCV in complex with alterations in B cells and follicular Th cell subsets may indicate a presence of autoimmunity in the pathogenesis of tuberculosis, but they are not specific. The indicators of autoimmune-related provide new opportunities in the Tbc treatment.

Indexed as

Autoimmune DiseasesMycobacterium tuberculosisTuberculosisTuberculosis, PulmonaryFlow CytometryHumansProspective StudiesRheumatoid FactorRheumatoid FactorautoantibodiesautoimmunityB-cellsTfh cellstrigger-factorstuberculosis

Identifiers

PMID36761174
PMCPMC9905676
OpenAlexW4317933058

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.