Evidence map›Paper›PMID 35686237›Full record

ArticleBioMed research international2022

Experimental Study of Potential CD8

Sidra Zafar, Baogang Bai, Jinlei Guo, Syed Aun Muhammad, Syeda Tahira Qousain Naqvi, Muhammad Nauman Shabbir, Imran Imran, Rehan Sadiq Shaikh, Amjad Ali

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Experimental trials of predicted CD4Frontiers in immunology · 2024
    Article
  3. Article
  4. 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

9 authors at 5 institutions in 2 countries.

Sidra ZafarInstitute of Molecular Biology and Biotechnology, Bahauddin Zakariya University, Multan, Pakistan.ORCID https://orcid.org/0000-0003-4877-995X
Baogang BaiSchool of Information and Technology, Wenzhou Business College, Wenzhou, Zhejiang, China.ORCID https://orcid.org/0000-0003-2802-0305
Jinlei GuoSchool of Medical Engineering, Sanquan College of Xinxiang Medical University, Henan, China.ORCID https://orcid.org/0000-0002-4594-9696
Syed Aun MuhammadInstitute of Molecular Biology and Biotechnology, Bahauddin Zakariya University, Multan, Pakistan.ORCID https://orcid.org/0000-0002-8068-4144
Syeda Tahira Qousain NaqviInstitute of Molecular Biology and Biotechnology, Bahauddin Zakariya University, Multan, Pakistan.ORCID https://orcid.org/0000-0002-7235-4102
Muhammad Nauman ShabbirDepartment of Statistics, Bahauddin Zakariya University, Multan, Pakistan.ORCID https://orcid.org/0000-0002-9031-1069
Imran ImranDepartment of Pharmacology, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan.ORCID https://orcid.org/0000-0003-1337-8574
Rehan Sadiq ShaikhCentre for Applied Molecular Biology, University of the Punjab, Lahore, Pakistan.ORCID https://orcid.org/0000-0003-3648-6965
Amjad AliAtta-ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad, Pakistan.ORCID https://orcid.org/0000-0002-0486-4661
Bahauddin Zakariya University · PKNational University of Sciences and Technology · PKUniversity of the Punjab · PKWenzhou University · CNXinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Liver cancer (LC) is the most devastating disease affecting a large set of populations in the world. The mortality due to LC is escalating, indicating the lack of effective therapeutic options. Immunotherapeutic agents may play an important role against cancer cells. As immune cells, especially T lymphocytes, which are part of cancer immunology, the design of vaccine candidates for cytotoxic T lymphocytes may be an effective strategy for curing liver cancer. Results: In our study, based on an immunoinformatics approach, we predicted potential T cell epitopes of MHC class I molecules using integrated steps of data retrieval, screening of antigenic proteins, functional analysis, peptide synthesis, and experimental Conclusion: We concluded that a potential therapeutic trivalent vaccine can activate and modulate the immune system to cure liver cancer on the basis of significant outcomes of specific and nonspecific assays.

Indexed as

Cancer VaccinesLiver NeoplasmsAnimalsEpitopes, T-LymphocyteHistocompatibility Antigens Class IImmunoglobulin GPeptidesRatsRats, Sprague-DawleyT-Lymphocytes, CytotoxicVaccine DevelopmentCancer VaccinesEpitopes, T-LymphocyteHistocompatibility Antigens Class IImmunoglobulin GPeptides

Identifiers

PMID35686237
PMCPMC9173915
OpenAlexW4283359580

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.