Evidence map›Paper›PMID 22197248›Full record

ArticleAntiviral research2012

The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine.

Ping Zhao, Dao-Xin Ma, Shuang Yu, Fu-Zhong Xue, Wei-Wei Zhu, Na Shao, Jing-Ru Zhang, Chun-Yan Ji

Abstract read
In one paragraph

Article in Antiviral research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Association between human cytomegalovirus and onset of epilepsy.International journal of clinical and experimental medicine · 2015
    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 3 institutions in 1 country.

Ping ZhaoDepartment of Hematology, Qilu Hospital, Shandong University, Jinan 250012, PR China; Department of Pediatrics, Provincial Hospital Affiliated to Shandong University, Jinan 250021, PR China.
Dao-Xin MaDepartment of Hematology, Qilu Hospital, Shandong University, Jinan 250012, PR China. Electronic address: daoxinma@sdu.edu.cn.
Shuang YuDepartment of Hematology, Qilu Hospital, Shandong University, Jinan 250012, PR China.
Fu-Zhong XueInstitute of Epidemiology and Health Statistics, School of Public Health of Shandong University, Jinan 250012, PR China.
Wei-Wei ZhuDepartment of Pediatrics, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, PR China.
Na ShaoDepartment of Hematology, Qilu Hospital, Shandong University, Jinan 250012, PR China.
Jing-Ru ZhangDepartment of Hematology, Qilu Hospital, Shandong University, Jinan 250012, PR China.
Chun-Yan JiDepartment of Hematology, Qilu Hospital, Shandong University, Jinan 250012, PR China. Electronic address: jichunyan@sdu.edu.cn.
Qilu Hospital of Shandong University · CNShandong University · CNShandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) infection is a major cause of morbidity in the recipients of organ transplants and in the congenitally infected infants. HCMV vaccine has emerged as an effective approach to prevent HCMV infection particularly for the development of multiple viral antigens vaccination and human leukocyte antigen (HLA)-restricted polyepitope technology. As the Chinese population makes up more than one fifth of the population worldwide, it is important to develop HCMV vaccines more specific for the Chinese population by targeting Chinese-restricted HLA alleles and antigens. In the present study, we designed a novel chimeric polyepitope vaccine based on the replication-deficient adenovirus Ad5F35, which encodes 83 HCMV T cell epitopes from 15 different HCMV antigens, restricted to 14 HLA I and 7 HLA II alleles that cover 92% of the Chinese population. Our results show that the recombinant adenovirus vaccine Ad5F35-CTL·Th can be efficiently transfected and expressed in peripheral blood mononuclear cells (PBMCs) with little cytopathic activity. Ad5F35-CTL·Th can also be endogenously processed and presented by PBMCs. Ad5F35-CTL·Th-stimulated HCMV-specific cytotoxic T lymphocytes (CTLs) showed strong cytolytic activity against HCMV polyepitope-sensitized target cells. The CTL activity was accompanied by high levels of IFN-γ production after Ad5F35-CTL·Th stimulation. The specificity and vigorous response to the recombinant adenovirus vaccine in vitro makes it a potential candidate to be used for transplantation recipients or congenitally infected infants.

Indexed as

Amino Acid SequenceAsian PeopleCell LineChinaCytomegalovirusCytomegalovirus InfectionsCytomegalovirus VaccinesEpitopes, T-LymphocyteHLA AntigensHumansMolecular Sequence DataSpecies SpecificityVaccines, SyntheticCytomegalovirus VaccinesEpitopes, T-LymphocyteHLA AntigensVaccines, Synthetic

Identifiers

PMID22197248
PMCPMC7114286
OpenAlexW1970878127

What OpenQuestion holds

Textmetadata
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.