Evidence map›Paper›PMID 37017116›Full record

ArticleCancer science2023

Pemetrexed combined with dual immune checkpoint blockade enhances cytotoxic T lymphocytes against lung cancer.

Mei-Chih Chen, Meng-Yu Hung, Chih-Ming Pan, Shi-Wei Huang, Chia-Ing Jan, Yu-Hsuan Li, Shao-Chih Chiu, Der-Yang Cho

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Immune cell engagers in lung cancer.Frontiers in immunology · 2026
    Review
  5. Article
  6. Metabolic Checkpoints in CD8International journal of biological sciences · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
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.

Mei-Chih ChenDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.ORCID https://orcid.org/0000-0002-8934-1236
Meng-Yu HungDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.
Chih-Ming PanDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.
Shi-Wei HuangDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.
Chia-Ing JanDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.
Yu-Hsuan LiDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.
Shao-Chih ChiuDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.
Der-Yang ChoDepartment of Medical Research, Translational Cell Therapy Center, China Medical University Hospital, Taichung, Taiwan.
China Medical University · TWNational Chung Hsing University · TW

Funding

China Medical University Hospital DMR-112-137China Medical University Hospital DMR-CELL-2107
6 · The paper itself

Abstract

Chemotherapy, in combination with immune checkpoint blockade (ICB) targeting to programmed death-1 (PD-1) or its ligand PD-L1, is one of the first-line treatments for patients with advanced non-small-cell lung cancer (NSCLC). However, a large proportion of patients, especially those with PD-L1 negative tumors, do not benefit from this treatment. This may be due to the existence of multiple immunosuppressive mechanisms other than the PD-1/PD-L1 axis. Human leukocyte antigen-G (HLA-G) has been identified as an immune checkpoint protein (ICP) and a neoexpressed tumor-associated antigen (TAA) in a large proportion of solid tumors. In this study, we evaluated the induction of HLA-G as well as PD-L1 using sublethal doses of chemotherapeutics including pemetrexed in different NSCLC cell lines. Except for gefitinib, most of the chemotherapeutic agents enhanced HLA-G and PD-L1 expression in a dose-dependent manner, whereas pemetrexed and carboplatin treatments showed the most consistent upregulation of PD-L1 and HLA-G in each cell line. In addition to protein levels, a novel finding of this study is that pemetrexed enhanced the glycosylation of HLA-G and PD-L1. Pemetrexed potentiated the cytotoxicity of cytotoxic T lymphocytes (CTLs) to treat NSCLC. Both in vitro and in vivo experiments revealed that CTL-mediated cytotoxicity was most pronounced when both anti-PD-L1 and anti-HLA-G ICBs were combined with pemetrexed treatment. In conclusion, anti-HLA-G could be an intervention strategy in addition to the anti-PD-1/PD-L1 pathway for NSCLC. Moreover, dual targeting of PD-L1 and HLA-G combined with pemetrexed might have a better extent of CTL-based immunotherapy.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenHumansImmune Checkpoint InhibitorsPemetrexedT-Lymphocytes, CytotoxicB7-H1 AntigenImmune Checkpoint InhibitorsPemetrexedCTLsHLA-GNSCLCPD-L1pemetrexed

Identifiers

PMID37017116
PMCPMC10323078
OpenAlexW4362601624

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.