Evidence map›Paper›PMID 37749867›Full record

ArticleAnnals of transplantation2023

Dynamic Changes of Regulatory T Cells/CD4⁺ T Cells in Peripheral Blood of Adult Kidney Transplant Recipients: A Comparison of Pediatric and Adult Kidney Donors.

Qi Xiao, Zide Chen, Shitao Zhao, Kaifeng Luo, Fuping Cao, Zexu Zhang, Jia Liu, Jiansheng Xiao

Open access · hybridAbstract read
In one paragraph

Article in Annals of transplantation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Qi XiaoDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
Zide ChenDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
Shitao ZhaoDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
Kaifeng LuoDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
Fuping CaoDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
Zexu ZhangDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
Jia LiuDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
Jiansheng XiaoDepartment of Transplantation, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).
First Affiliated Hospital of Nanchang University · CNNanchang University · CN

Funding

Identifying Approaches to Measure and Reduce Harmful, Low-Value Care Among Older Americans with Mild Cognitive Impairment and DementiaR01AG070017 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MAFI, JOHN N. · 2021 to 2025
$2.6M
NIA NIH HHS R01 AG070017
6 · The paper itself

Abstract

BACKGROUND Inducing transplantation tolerance and monitoring the recipient's immune status to improve allograft survival remains the main goal for kidney transplantation (KTx). MATERIAL AND METHODS A total of 53 renal transplantation patients and 20 healthy individuals were assigned to the post-transplantation and healthy groups, respectively; 10 recipients with stable renal function for 2 years after kidney transplantation were assigned to Group C. Eleven kidney transplantation recipients were hospitalized due to lung infection. Flow cytometry was used to measure levels of Tregs/CD4⁺ T cells. RESULTS The Tregs/CD4⁺ T cells ratio reached homeostasis 6 months after KTx, with no significant difference between Group D (healthy control group) and pre-surgery or Group C (2 years after KTx group). The pediatric donor group and the adult donor group reached immune homeostasis 3 months after the operation. Immune homeostasis is maintaining a balance between immune tolerance and immunogenicity. There was no significant difference in graft function between the pediatric and adult donor groups before surgery, 1 day after surgery, 1 week after surgery, 2 weeks after surgery, and 1 month after surgery; however, graft function was significantly better in the pediatric donor group compared with the adult donor group at 3 mouths (eGFR: 51.7 (40.4-66.2) vs 73.0 (55.7-90.2), P=0.008<0.05) and 6 months (eGFR: 52.2 (37.5-62.8) vs 80.5 (64.1-90.4), P<0.001) after surgery. Pediatric donor kidneys reached immune homeostasis 3 months after surgery, with better graft function at this time compared with adult donor kidneys. The proportion of Tregs/CD4⁺ T cells in recipients with a pulmonary infection after KTx was lower than in those with infection recovery. CONCLUSIONS Expanding the use of pediatric kidneys should be further explored by the transplantation community. The proportion of Tregs/CD4⁺ T cells in recipients with a pulmonary infection after KTx was lower than in those with infection recovery.

Indexed as

Kidney TransplantationT-Lymphocytes, RegulatoryAdultCD4-Positive T-LymphocytesChildHumansTissue DonorsTransplant Recipients

Identifiers

PMID37749867
PMCPMC10541792
OpenAlexW4386476169

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.