Evidence map›Paper›PMID 35935985›Full record

ArticleFrontiers in immunology2022

The interaction between the soluble programmed death ligand-1 (sPD-L1) and PD-1

Xuejiao Li, Huan Du, Shenghua Zhan, Wenting Liu, Zhangyu Wang, Jing Lan, Longxiang PuYang, Yuqiu Wan, Qiuxia Qu, Sining Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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  5. Pro-Resolving Macrophage-Induced IL-35International journal of molecular sciences · 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

13 authors at 5 institutions in 1 country.

Xuejiao LiSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Huan DuSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Shenghua ZhanDepartment of Pathology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Wenting LiuSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Zhangyu WangDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, China.
Jing LanDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, China.
Longxiang PuYangSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Yuqiu WanSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Qiuxia QuJiangsu Institute of Clinical Immunology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Sining WangSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Yang YangSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Qin WangSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Fang XieSchool of Biology & Basic Medical Sciences, Medical College of Soochow University, Suzhou, China.
Soochow University · CNFirst Affiliated Hospital of Soochow University · CNHuashan Hospital · CNShanghai Jiao Tong University · CNThe First People’s Hospital of Lianyungang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence suggests that regulatory B cells (Bregs) play important roles in inhibiting the immune response in tumors. Programmed death 1 (PD-1) and programmed death ligand 1 (PD-L1) are important molecules that maintain the balance of the immune response and immune tolerance. This study aims to evaluate the soluble form of PD-L1 and its function in inducing the differentiation of B lymphocytes, investigate the relationship between soluble PD-L1 (sPD-L1) and B-cell subsets, and explore the antitumor activity of T lymphocytes after PD-L1 blockade in coculture systems. In an effort to explore the role of sPD-L1 in human breast cancer etiology, we examined the levels of sPD-L1 and interleukin-10 (IL-10) in the serum of breast tumor patients and the proportions of B cells, PD-1

Indexed as

B-Lymphocytes, RegulatoryImmunologic Deficiency SyndromesTriple Negative Breast NeoplasmsB7-H1 AntigenHumansImmune ToleranceImmunosuppression TherapyInterleukin-10Programmed Cell Death 1 ReceptorB7-H1 AntigenCD274 protein, humanInterleukin-10Programmed Cell Death 1 ReceptorimmunosuppressionPD-1+ regulator B cellsregulator T cellsPD-L1the triple-negative breast cancer

Identifiers

PMID35935985
PMCPMC9354578
OpenAlexW4286697758

What OpenQuestion holds

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LicenceCC BY
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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.