Evidence map›Paper›PMID 22278837›Full record

ArticleJournal of clinical microbiology2012

Development of a human herpesvirus 6 species-specific immunoblotting assay.

Yuki Higashimoto, Akane Ohta, Yukihiro Nishiyama, Masaru Ihira, Ken Sugata, Yoshizo Asano, Daniel L Peterson, Dharam V Ablashi, Paolo Lusso, Tetsushi Yoshikawa

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. New strategies against drug resistance to herpes simplex virus.International journal of oral science · 2016
    Review
  4. Review
  5. Review
  6. 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

10 authors at 5 institutions in 3 countries.

Yuki HigashimotoDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Akane Ohta
Yukihiro Nishiyama
Masaru Ihira
Ken Sugata
Yoshizo Asano
Daniel L Peterson
Dharam V Ablashi
Paolo Lusso
Tetsushi Yoshikawa
Fujita Health University · JPNagoya University · JPHHV-6 Foundation · USNational Institute of Allergy and Infectious Diseases · USSierra Nevada College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to assess the full spectrum of human herpesvirus 6A (HHV-6A)- and HHV-6B-associated diseases, we sought to develop an HHV-6 species-specific serological assay based on immunoblot analysis. The immunodominant proteins encoded by open reading frame U11, p100 for HHV-6A (strain U1102) and 101K for HHV-6B (strain Z29), were selected to generate virus species-specific antigens. Recombinant p100 and 101K were produced in a prokaryotic expression system. The expression of these proteins was confirmed by using anti-His tag and 101K-specific monoclonal antibodies. HHV-6 species-specific antibodies were detected by immunoblotting in patient sera. Eighty-seven serum samples obtained from various subjects were utilized to determine the reliability of the method for clinical use. Ten of twelve exanthem subitum convalescent-phase sera reacted exclusively with 101K, whereas none of twelve acute-phase sera reacted with either protein. Two of three sera collected from HHV-6A-infected patients reacted with p100 and 101K. Although all five acute and convalescent-phase sera obtained from transplant recipients reacted exclusively with 101K, two of six convalescent-phase sera obtained from patients with drug-induced hypersensitivity syndrome reacted with both p100 and 101K. Of 38 sera obtained from healthy adults, 31 were positive for 101K antibody, while 4 reacted with both proteins. However, PCR analysis of peripheral blood mononuclear cells and saliva from these subjects did not detect HHV-6A DNA. In conclusion, this novel serological assay based on immunoblot analysis using recombinant HHV-6A p100 and HHV-6B 101K allowed us to discriminate between HHV-6A- and HHV-6B-specific antibodies.

Indexed as

AdolescentAdultAgedAntibodies, ViralAntigens, ViralBlotting, WesternCells, CulturedChildChild, PreschoolDNA, ViralExanthema SubitumFemaleHerpesvirus 6, HumanHumansInfantLeukocytes, MononuclearAntibodies, ViralAntigens, ViralDNA, Viral

Identifiers

PMID22278837
PMCPMC3318559
OpenAlexW2086658817

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.