Evidence map›Paper›PMID 38467886›Full record

ArticleBiochemical genetics2025

Assessment of CTLA-4 Gene Expression Levels on CD8+ T Cells in Renal Transplant Patients and Relation with Serum sCTLA-4 Levels.

Burcu Çerçi Alkaç, Mustafa Soyöz, Melek Pehlivan, Tülay Kılıçaslan Ayna, Erhan Tatar, H İlayhan Karahan Çöven, Mehmet Tanrısev, İbrahim Pirim

Abstract read
PubMed Publisher
In one paragraph

Article in Biochemical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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.

Burcu Çerçi AlkaçDepartment of Medical Biology, Faculty of Medicine, Izmir Katip Celebi University, Izmir, Türkiye. burcu.cerci@ikcu.edu.tr.
Mustafa SoyözDepartment of Medical Biology, Faculty of Medicine, Izmir Katip Celebi University, Izmir, Türkiye.
Melek PehlivanVocational School of Health Services, Izmir Katip Celebi University, Izmir, Türkiye.
Tülay Kılıçaslan AynaDepartment of Medical Biology, Faculty of Medicine, Izmir Katip Celebi University, Izmir, Türkiye.
Erhan TatarDepartment of Nephrology, Bozyaka Training and Research Hospital, University of Health Science, Izmir, Türkiye.
H İlayhan Karahan ÇövenDepartment of Medical Biology, Faculty of Medicine, Izmir Katip Celebi University, Izmir, Türkiye.
Mehmet TanrısevDepartment of Nephrology, Tepecik Training and Research Hospital, University of Health Science, Izmir, Türkiye.
İbrahim PirimDepartment of Medical Biology, Faculty of Medicine, Izmir Katip Celebi University, Izmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CTLA-4 (Cytotoxic T Lymphocyte Antigen-4) is an immune regulator molecule that is expressed on a variety of immune cells, including CD4+ and CD8+ T cells. After realizing the significance of this regulator molecule, researchers began to concentrate on its activation or inhibition in cancer. Even though there have been some studies on organ transplantation and autoimmunity, the role of the CTLA-4 molecule in renal transplantation has not been demonstrated. The goal of this study was to see how CTLA-4 gene expression and serum sCTLA-4 levels affected renal transplant patients. Peripheral blood samples were collected before and 1-3 months after renal transplantation from 29 recipients. CD8+ T lymphocytes were separated using magnetic beads and purity of the cells controlled by Flow cytometry. CTLA-4 mRNA levels were determined by Real-Time PCR while serum sCTLA-4 levels were assessed by ELISA. 55% of the patient had decreased level of CTLA-4 mRNA after transplantation when compared to pre-transplantation levels. Moreover 61% of the patient had lower serum sCTLA-4 levels after transplantation. sCTLA-4 levels were decreased 11% of the patients with rejection episode after transplantation when compared to stabile patients (5%). Kidney rejection is a complicated process influenced by numerous unknown factors. Several parameters should be evaluated together to precise rejection episodes or graft dysfunctions. Further research focused on the other immune checkpoint regulator molecules could give an opportunity to have an idea about the effect of these molecules on renal transplantation.

Indexed as

CD8-Positive T-LymphocytesCTLA-4 AntigenGraft RejectionKidney TransplantationAdultFemaleGene Expression RegulationHumansMaleMiddle AgedRNA, MessengerCTLA-4 AntigenCTLA4 protein, humanRNA, MessengerCD8+ T cellsCTLA-4Renal transplantation

Identifiers

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.