Evidence map›Paper›PMID 26321864›Full record

ArticleMolecular vision2015

Programmed Death 1 (PD-1) is involved in the development of proliferative diabetic retinopathy by mediating activation-induced apoptosis.

Mengyuan Fang, Qianli Meng, Haike Guo, Liya Wang, Zhaoxia Zhao, Liang Zhang, Jian Kuang, Ying Cui, Liping Mai, Jiening Zhu

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

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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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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 1 institution in 1 country.

Mengyuan FangSouthern Medical University, Guangzhou, China ; Guangdong Eye Institute, Department of Ophthalmology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Qianli MengGuangdong Eye Institute, Department of Ophthalmology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Haike GuoGuangdong Eye Institute, Department of Ophthalmology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Liya WangHenan Eye Institute, Henan Eye Hospital, Zhengzhou, China.
Zhaoxia ZhaoHenan Eye Institute, Henan Eye Hospital, Zhengzhou, China.
Liang ZhangGuangdong Eye Institute, Department of Ophthalmology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Jian KuangDepartment of endocrinology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Ying CuiGuangdong Eye Institute, Department of Ophthalmology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Liping MaiResearch Center of Medicine, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Jiening ZhuResearch Center of Medicine, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Henan Provincial Eye Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRecent studies revealed that immunological mechanisms play a prominent role in the pathogenesis of proliferative diabetic retinopathy (PDR). Given the importance of the immune response in PDR and the significance of the programmed death 1 (PD-1) pathway as an immune regulatory pathway, the aim of this study is to determine the expression and functional characteristics of the PD-1 pathway in peripheral blood lymphocytes from patients with PDR.

methodsPeripheral blood lymphocytes were obtained from patients with PDR, age-matched patients with diabetes mellitus and no diabetic retinopathy (DM-NDR), and controls. The mRNA expression of PD-1 and its ligands were determined using real-time PCR. The frequencies of PD-1 and its ligands, activation-induced apoptosis, IFN-γ, and IL-4 were determined by flow cytometry.

resultsThe PD-1 mRNA expression markedly decreased, while the frequency of PD-1(+) cells increased in the PDR group compared with the DM-NDR and control groups. The expression of PD-ligand 1 (PD-L1) mRNA and PD-L1(+) cells in the PDR group was lower than that in the other two groups. In the PDR group, the frequency of Annexin V(+)PI(-) and Annexin V(+)PI(-)PD-1(+) cells increased, while the frequency of Annexin V(+)PI(-)PD-L1(+) cells decreased. Although their expression was upregulated, the ratio of PD-1(+) IFN-γ(+) to PD-1(+)IL-4(+) cells in the PDR group was not significantly different to that in the DM-NDR and control groups.

conclusionsThese results suggest that PD-1 is involved in the development of PDR by mediating activation-induced apoptosis.

Indexed as

AdultAgedApoptosisCase-Control StudiesDiabetic RetinopathyFemaleHumansLigandsLymphocyte ActivationLymphocytesMaleMiddle AgedProgrammed Cell Death 1 ReceptorReal-Time Polymerase Chain ReactionRNA, MessengerLigandsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorRNA, Messenger

Identifiers

PMID26321864
PMCPMC4544714
OpenAlexW1205932074

What OpenQuestion holds

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Registered trials

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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.