Evidence map›Paper›PMID 29167005›Full record

ArticleZhongguo fei ai za zhi = Chinese journal of lung cancer2017

[Distribution and Clinical Significance of CTLA-4, PD-1 and PD-L1 in Peripheral Blood of Patients with Small Cell Lung Cancer].

Hui Li, Yan Liu, Ying Liu, Jingjing Liu, Dandan Zhao, Ying Wang, Ying Cheng

Open access · greenAbstract read
In one paragraph

Article in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 4 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

7 authors at 1 institution in 1 country.

Hui LiMedical Oncology Translational Research Lab, Jilin Cancer Hospital, 
Changchun 130012, China.
Yan LiuMedical Oncology Translational Research Lab, Jilin Cancer Hospital, 
Changchun 130012, China.
Ying LiuDepartment of Medical Thoracic Oncology, Jilin Cancer Hospital, 
Changchun 130012, China.
Jingjing LiuDepartment of Medical Thoracic Oncology, Jilin Cancer Hospital, 
Changchun 130012, China.
Dandan ZhaoMedical Oncology Translational Research Lab, Jilin Cancer Hospital, 
Changchun 130012, China.
Ying WangDepartment of Medical Thoracic Oncology, Jilin Cancer Hospital, 
Changchun 130012, China.
Ying ChengDepartment of Medical Thoracic Oncology, Jilin Cancer Hospital, 
Changchun 130012, China.
Jilin Province Tumor Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study is to explore cytotoxic T lymphocyte associated antigen 4 (CTLA-4), programmed death 1 (PD-1) and programmed death ligand 1 (PD-L1) distribution and clinical value in liquid biopsy (such as blood) of small cell lung cancer (SCLC) patients.

methodsA total of 60 healthy and 290 chemotherapy-naive patients with SCLC were recruited. Venous blood samples were collected prior to chemotherapy (baseline) and after the second cycle of chemotherapy (2nd cycle), and flow cytometry was used to analyze the level of CTLA-4, PD-1 or PD-L1 with or without CD3, CD4, CD8 or CD25. Immunocytochemical method was used to detect PD-L1 expression in SCLC cell line H446.

resultsCells of CTLA-4+ and PD-1+ in SCLC peripheral blood were (1.56±1.24)% and (8.07±3.97)%; there is no significant difference between CD3+CTLA-4+ and CD4+CTLA-4+, (4.87±5.18)% and (3.85±2.60)%, but show lower expression than CD3+PD-1+ and CD4+PD-1+ (26.63±9.04)% and (20.79±9.41)%, respectively. However, the level of CD4+CD25+CTLA-4+ cells were remarkably higher in SCLC than that in control, (7.09±5.09)% vs (1.91±1.27)%, P<0.001 and CD8+PD-1+ cells were less in SCLC than that in control, (11.47±5.85)% vs (22.56±4.21)%, P<0.001, both of which were not associated with age, sex, smoke or disease stage. Level of CD4+CD25+CTLA-4+ cells and CD8+PD-1+ cells was dropped (5.11±2.60)% vs (6.94±4.91)% and (8.74±3.39)% vs (11.48±5.91)% after 2nd cycle compare to that at baseline (P<0.000,1). Neither the level of CD4+CD25+CTLA-4+ nor CD8+PD-1+ cells before or after treatment was related to progression-free disease or overall survival of patients. Although PD-L1 was highly expressed in H446 cell cytoplasm and membrane, it was rarely found in peripheral blood.

conclusionsThe data we presented here showed that CTLA-4 was highly expressed in regulatory T cells and PD-1 decreased in CD8+ T cells in peripheral blood of SCLC patients, suggesting their unique mechanisms involved in immune regulation. CD4+CD25+CTLA-4+ level changed after treatment implies its potential role in predicting treatment efficacy.
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Indexed as

AdultAgedB7-H1 AntigenBiomarkers, TumorCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorCTLA-4 AntigenFemaleHumansInterleukin-2 Receptor alpha SubunitLung NeoplasmsMaleMiddle AgedProgrammed Cell Death 1 ReceptorSmall Cell Lung CarcinomaB7-H1 AntigenBiomarkers, TumorCD274 protein, humanCTLA-4 AntigenInterleukin-2 Receptor alpha SubunitPDCD1 protein, humanProgrammed Cell Death 1 ReceptorbiomarkerCTLA-4PD-1PD-L1SCLC

Identifiers

PMID29167005
PMCPMC5973273
OpenAlexW2994724794

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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.