Evidence map›Paper›PMID 34830017›Full record

ArticleInternational journal of molecular sciences2021

Impaired Innate Immunity in Pediatric Patients Type 1 Diabetes-Focus on Toll-like Receptors Expression.

Katarzyna Kurianowicz, Maria Klatka, Agnieszka Polak, Anna Hymos, Dominika Bębnowska, Martyna Podgajna, Rafał Hrynkiewicz, Olga Sierawska, Paulina Niedźwiedzka-Rystwej

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 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
1.4field-weighted citation impact, top 17% 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, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. 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

9 authors at 2 institutions in 1 country.

Katarzyna KurianowiczDepartment of Pediatric Endocrinology and Diabetology, Medical University of Lublin, Gębali 1 St., 20-093 Lublin, Poland.ORCID 0000-0002-7840-9645
Maria KlatkaDepartment of Pediatric Endocrinology and Diabetology, Medical University of Lublin, Gębali 1 St., 20-093 Lublin, Poland.ORCID 0000-0002-2743-8139
Agnieszka PolakDepartment of Endocrinology, Medical University of Lublin, Jaczewskiego 8 St., 20-954 Lublin, Poland.ORCID 0000-0003-1694-4738
Anna HymosDepartment of Experimental Immunology, Medical University of Lublin, Chodźki 4a St., 20-093 Lublin, Poland.
Dominika BębnowskaInstitute of Biology, University of Szczecin, 71-412 Szczecin, Poland.ORCID 0000-0003-3689-2381
Martyna PodgajnaDepartment of Clinica Immunology and Immunotherapy, Medical University of Lublin, Chodźki 4a St., 20-093 Lublin, Poland.
Rafał HrynkiewiczInstitute of Biology, University of Szczecin, 71-412 Szczecin, Poland.ORCID 0000-0002-0688-6928
Olga SierawskaInstitute of Biology, University of Szczecin, 71-412 Szczecin, Poland.ORCID 0000-0003-3567-7786
Paulina Niedźwiedzka-RystwejInstitute of Biology, University of Szczecin, 71-412 Szczecin, Poland.ORCID 0000-0003-4065-3842
Medical University of Lublin · PLUniversity of Szczecin · PL

Funding

Medical University of Lublin DS460
6 · The paper itself

Abstract

Type 1 diabetes (DM1) is classified as an autoimmune disease. An uncontrolled response of B and T lymphocytes to the body's own tissues develops in the absence of immune tolerance. The main aim of the study was to evaluate the effect of the duration of type 1 diabetes in children on the expression of TLR receptors and the relationship with the parameters of glycemic control in patients. As a result, we showed significant differences in the level of TLR2, TLR4 and TLR9 expression in patients with DM1 in the early stage of the disease and treated chronically compared to the healthy group. Additionally, in this study, we found that the numbers of CD19+ B cells, CD3+ CD4+, CD3+ CD8+ T cells and NK cells are different for newly diagnosed DM1 individuals, patients receiving chronic treatment and for healthy controls, indicating an important role of these cells in killing pancreatic beta cells. Moreover, higher levels of IL-10 in patients with newly diagnosed DM1 have also been found, confirming the reports found in the literature.

Indexed as

AdolescentAntigens, CD19B-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChildChild, PreschoolDiabetes Mellitus, Type 1FemaleGene Expression RegulationHumansImmunity, InnateInterleukin-10Killer Cells, NaturalMalePediatricsAntigens, CD19IL10 protein, humanInterleukin-10TLR2 protein, humanTLR4 protein, humanToll-Like Receptor 2Toll-Like Receptor 4Toll-Like Receptor 9Toll-Like ReceptorschildrenToll-like receptorstype 1 diabetes mellitus

Identifiers

PMID34830017
PMCPMC8625857
OpenAlexW3213881998

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.