Evidence map›Paper›PMID 30969023›Full record

ArticleCancer medicine2019

Circulating PD-1 (+) cells may participate in immune evasion in peripheral T-cell lymphoma and chidamide enhance antitumor activity of PD-1 (+) cells.

Wei Zhang, Haorui Shen, Yan Zhang, Wei Wang, Shaoxuan Hu, Dongmei Zou, Daobin Zhou

Abstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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.

Wei ZhangDepartment of Hematology, Peking Union Medical College Hospital, Beijing, P.R. China.
Haorui ShenDepartment of Hematology, Peking Union Medical College Hospital, Beijing, P.R. China.ORCID 0000-0003-4330-850X
Yan ZhangDepartment of Hematology, Peking Union Medical College Hospital, Beijing, P.R. China.
Wei WangDepartment of Hematology, Peking Union Medical College Hospital, Beijing, P.R. China.ORCID 0000-0002-1192-4896
Shaoxuan HuDepartment of Hematology, Peking Union Medical College Hospital, Beijing, P.R. China.
Dongmei ZouDepartment of Hematology, Peking Union Medical College Hospital, Beijing, P.R. China.
Daobin ZhouDepartment of Hematology, Peking Union Medical College Hospital, Beijing, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral T-cell lymphoma (PTCL) is a heterogeneous disease with poor outcomes. We intend to explore the role of circulating PD-1 (+) cells in tumor immune evasion in PTCL patients and the mechanism of chidamide as a regulator of immune-associated medicine on PD-1 (+) cells. Gene expression profiling (GEP) was performed on circulating PD-1 (+) cells from 22 PTCL patients and 13 healthy subjects, and circulating PD-1 (-) cells from 2 PTCL patients. PD-1 (+) cells were treated with chidamide, and the production IFN-γ and cytotoxicity were analyzed. GEP were performed on circulating PD-1 (+) cells from 2 PTCL patients treated with chidamide combined with chemotherapy and 1 patient treated with traditional chemotherapy. GEP showed that genes associated with innate immune response were abnormally expressed in PD-1 (+) cells of PTCL patients compared with healthy subjects, meanwhile the expression of CTLA-4 was significantly higher in PD-1 (+) cells than that of PD-1 (-) cells. In vitro study revealed decreased level of IFN-γ secretion and impaired cytotoxic activity of PD-1 (+) cells compared with PD-1 (-) cells, while chidamide could recover the deficiencies and upregulate adaptive immune-associated genes in PD-1 (+) cells of PTCL patients. Our research indicated that PD-1 (+) cells might have deficiencies in innate and adaptive immune response and chidamide may reverse the defects.

Indexed as

Adaptive ImmunityAdultAgedAminopyridinesAntineoplastic AgentsBenzamidesCase-Control StudiesCTLA-4 AntigenFemaleGene Expression Regulation, NeoplasticHumansInterferon-gammaK562 CellsLymphoma, T-Cell, PeripheralMaleMiddle AgedAminopyridinesAntineoplastic AgentsBenzamidesCTLA-4 AntigenCTLA4 protein, humanIFNG protein, humanInterferon-gammaN-(2-amino-5-fluorobenzyl)-4-(N-(pyridine-3-acrylyl)aminomethyl)benzamidePDCD1 protein, humanProgrammed Cell Death 1 Receptoradaptive immunechidamideinnate immuneperipheral T-cell lymphomaprogrammed cell death-1

Identifiers

PMID30969023
PMCPMC6536954

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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.