Evidence map›Paper›PMID 33804135›Full record

ArticleInternational journal of molecular sciences2021

CD28null and Regulatory T Cells Are Substantially Disrupted in Patients with End-Stage Renal Disease Due to Diabetes Mellitus.

Erasmia Sampani, Dimitra-Vasilia Daikidou, George Lioulios, Aliki Xochelli, Zoi Mitsoglou, Vasiliki Nikolaidou, Chrysostomos Dimitriadis, Asimina Fylaktou, Aikaterini Papagianni, Maria Stangou

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Lower absolute numbers of CD4Renal failure · 2025
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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 2 institutions in 1 country.

Erasmia SampaniDepartment of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, 56442 Thessaloniki, Greece.
Dimitra-Vasilia DaikidouDepartment of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, 56442 Thessaloniki, Greece.
George LiouliosDepartment of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, 56442 Thessaloniki, Greece.
Aliki XochelliNational Peripheral Histocompatibility Center, Department of Immunology, Hippokration Hospital, 56442 Thessaloniki, Greece.
Zoi MitsoglouDepartment of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, 56442 Thessaloniki, Greece.
Vasiliki NikolaidouNational Peripheral Histocompatibility Center, Department of Immunology, Hippokration Hospital, 56442 Thessaloniki, Greece.
Chrysostomos DimitriadisDepartment of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, 56442 Thessaloniki, Greece.
Asimina FylaktouNational Peripheral Histocompatibility Center, Department of Immunology, Hippokration Hospital, 56442 Thessaloniki, Greece.
Aikaterini PapagianniDepartment of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, 56442 Thessaloniki, Greece.
Maria StangouDepartment of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, 56442 Thessaloniki, Greece.ORCID 0000-0003-2496-9863
Aristotle University of Thessaloniki · GRHippocration General Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnd-stage renal disease (ESRD) is associated with alterations in T-cell immunity, including increased CD28null and reduced regulatory T cells (Tregs). However, whether immune disturbances are due to ESRD or primary disease is not yet clear. As diabetes mellitus is the leading cause of ESRD, we evaluated its impact on the immune profile of ESRD patients.

methodsCD28null, Tregs, and natural killer cells were initially analyzed by flow cytometry in 30 predialysis ESRD patients due to diabetes (DM), 30 non-DM (NDM), and 25 healthy controls. Measurements were repeated after 6 months on hemodialysis (HD) or peritoneal dialysis (CAPD).

resultsThe percentage of CD4 + CD28null cells, CD8 + CD28null cells, and Tregs showed significant differences in DM, NDM, and controls; mean rank 33.71 vs. 25.68 vs. 18.88,

conclusionsDiabetes mellitus affects T-cell subtypes even at predialysis stage, though changes become more prominent after commencement on HD.

Indexed as

AdultCD28 AntigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDiabetes ComplicationsDiabetes MellitusFemaleFlow CytometryHumansKidney Failure, ChronicKiller Cells, NaturalMaleMiddle AgedRenal DialysisT-Lymphocytes, RegulatoryCD28 AntigensCD28null cellsdiabetes mellitusend-stage renal diseaselymphocytesregulatory T cells

Identifiers

PMID33804135
PMCPMC8001943
OpenAlexW3139509699

What OpenQuestion holds

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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.