Evidence map›Paper›PMID 33028368›Full record

ArticleVirology journal2020

Protective CD8

Ying Ma, Kang Tang, Yusi Zhang, Chunmei Zhang, Linfeng Cheng, Fanglin Zhang, Ran Zhuang, Boquan Jin, Yun Zhang

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.2field-weighted citation impact, top 36% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Development of a vaccine construct againstNAR genomics and bioinformatics · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Correlation analysis of CD8Frontiers in pediatrics · 2023
    Article
  9. Article
  10. IL-15 induced bystander activation of CD8Frontiers in cellular and infection microbiology · 2022
    Article
  11. 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 1 institution in 1 country.

Ying MaDepartment of Immunology, The Fourth Military Medical University, 169 Changle West Road, Xi'an, 710032, China. mayingying@fmmu.edu.cn.ORCID 0000-0002-1936-3982
Kang TangDepartment of Immunology, The Fourth Military Medical University, 169 Changle West Road, Xi'an, 710032, China.
Yusi ZhangDepartment of Immunology, The Fourth Military Medical University, 169 Changle West Road, Xi'an, 710032, China.
Chunmei ZhangDepartment of Immunology, The Fourth Military Medical University, 169 Changle West Road, Xi'an, 710032, China.
Linfeng ChengDepartment of Microbiology, The Fourth Military Medical University, Xi'an, 710032, China.
Fanglin ZhangDepartment of Microbiology, The Fourth Military Medical University, Xi'an, 710032, China.
Ran ZhuangDepartment of Immunology, The Fourth Military Medical University, 169 Changle West Road, Xi'an, 710032, China.
Boquan JinDepartment of Immunology, The Fourth Military Medical University, 169 Changle West Road, Xi'an, 710032, China.
Yun ZhangDepartment of Immunology, The Fourth Military Medical University, 169 Changle West Road, Xi'an, 710032, China. immuzy@fmmu.edu.cn.
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn effective vaccine that prevents disease caused by hantaviruses is a global public health priority, but up to now, no vaccine has been approved for worldwide use. Therefore, novel vaccines with high prophylaxis efficacy are urgently needed.

methodsHerein, we designed and synthesized Hantaan virus (HTNV) linear multi-epitope peptide consisting of HLA-A*02-restricted HTNV cytotoxic T cell (CTL) epitope and pan HLA-DR-binding epitope (PADRE), and evaluated the immunogenicity, as well as effectiveness, of multi-epitope peptides in HLA-A2.1/K

resultsThe results showed that a much higher frequency of specific IFN-γ-secreting CTLs, high levels of granzyme B production, and a strong proliferation capacity of specific CTLs were observed in splenocytes of mice immunized with multi-epitope peptide than in those of a single CTL epitope. Moreover, pre-immunization of multi-epitope peptide could reduce the levels of HTNV RNA loads in the liver, spleen and kidneys of mice, indicating that specific CTL responses induced by multi-epitope peptide could reduce HTNV RNA loads in vivo.

conclusionsThis study may provide an important foundation for the development of novel peptide vaccines for HTNV prophylaxis.

Indexed as

AnimalsAntigens, ViralCD8-Positive T-LymphocytesEpitopes, T-LymphocyteHantaan virusHemorrhagic Fever with Renal SyndromeHLA-A2 AntigenImmunizationMalaria VaccinesMaleMiceMice, TransgenicT-Lymphocytes, CytotoxicVaccines, SubunitAntigens, ViralEpitopes, T-LymphocyteHLA-A2 AntigenMalaria VaccinesPADRE 45Vaccines, SubunitCytotoxic T cell responseHantaan virusHLA-A2.1/Kb transgenic miceMulti-epitope peptideVaccine

Identifiers

PMID33028368
PMCPMC7538842
OpenAlexW3092276261

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.