Evidence map›Paper›PMID 29435173›Full record

ArticleOncotarget2018

CRISPR knock out of programmed cell death protein 1 enhances anti-tumor activity of cytotoxic T lymphocytes.

Zhilong Zhao, Long Shi, Wei Zhang, Jinsheng Han, Shaohui Zhang, Zexian Fu, Jianhui Cai

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

55 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Frontiers in immunology · 2026
    Review
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Are we there yet? CAR-T therapy in multiple myeloma.British journal of haematology · 2024
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Employing CRISPR-Cas9 to Enhance T Cell Effector Function.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  17. Review
  18. Article
  19. Article
  20. 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

7 authors at 6 institutions in 1 country.

Zhilong ZhaoDepartment of Surgery, Hebei Medical University, Shijiazhuang, Hebei, China.
Long ShiDepartment of Oncology, Hebei Medical University Second Affiliated Hospital, Shijiazhuang, Hebei, China.
Wei ZhangDepartment of Surgery, Handan Central Hospital, Handan, Hebei, China.
Jinsheng HanDepartment of Surgery, Cangzhou Hospital of Traditional Chinese Medicine and Western Medicine Integrated Hebei, Cangzhou, Hebei, China.
Shaohui ZhangDepartment of Oncology, Hebei Medical University Third Affiliated Hospital, Shijiazhuang, Hebei, China.
Zexian FuDepartment of Oncology, Hebei University of Engineering Affiliated Hospital, Baoding, Hebei, China.
Jianhui CaiDepartment of Surgery, Hebei Medical University, Shijiazhuang, Hebei, China.
Hebei Medical University · CNHandan College · CNHebei General Hospital · CNHebei University of Engineering · CNPeople's Hospital of Cangzhou · CNThird Hospital of Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed cell death protein 1 (PD-1) is an immune checkpoint receptor that functions to attenuate T cell activation. In this study, we knocked out (KO) PD-1 in cytotoxic T lymphocytes (CTLs) using CRISPR-Cas9 system to evaluate its effect on the anti-tumor activity of the CTLs against multiple myeloma (MM). Results show that PD-1 KO CTLs facilitate apoptosis and caspase activation of the co-cultured MM cells and enhanced MM cell death by 36% compared with the control. PD-1 KO also increased TNF-α and IFN-γ secretion of the CTLs by 2.4 and 1.9-fold respectively. The effectiveness of PD-1 KO in enhancing anti-tumor activity of the CTLs was verified

Indexed as

anti-tumor immunityCRISPRcytotoxic T lymphocyteimmune checkpointPD-1

Identifiers

PMID29435173
PMCPMC5797044
OpenAlexW2778493760

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.