Evidence map›Paper›PMID 25708705›Full record

ArticleImmunobiology2015

Development and characterization of a panel of cross-reactive monoclonal antibodies generated using H1N1 influenza virus.

Chun-yan Guo, Yi-gui Tang, Zong-li Qi, Yang Liu, Xiang-rong Zhao, Xue-ping Huo, Yan Li, Qing Feng, Peng-hua Zhao, Xin Wang and 4 more

Abstract read
In one paragraph

Article in Immunobiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. H1N1 influenza virus epitopes classified by monoclonal antibodies.Experimental and therapeutic medicine · 2018
    Article
  8. 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

14 authors at 3 institutions in 2 countries.

Chun-yan GuoCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Yi-gui TangCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Zong-li QiCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Yang LiuCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Xiang-rong ZhaoCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Xue-ping HuoCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Yan LiCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Qing FengCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Peng-hua ZhaoCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Xin WangCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Yuan LiCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Hai-fang WangCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China.
Jun HuCentral Lab of Shaanxi Provincial People's Hospital, The Third Affiliated Hospital of the Medical College of Xi'an Jiaotong University, Key Laboratory of Infection and Immunity Disease of Shaanxi Province, Xi'an 710068, China. Electronic address: hjj6562@63.com.
Xin-jian ZhangCenters for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, United States.
Shaanxi Provincial People's Hospital · CNXi'an Jiaotong University · CNCenters for Disease Control and Prevention · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To characterize the antigenic epitopes of the hemagglutinin (HA) protein of H1N1 influenza virus, a panel consisting of 84 clones of murine monoclonal antibodies (mAbs) were generated using the HA proteins from the 2009 pandemic H1N1 vaccine lysate and the seasonal influenza H1N1(A1) vaccines. Thirty-three (39%) of the 84 mAbs were found to be strain-specific, and 6 (7%) of the 84 mAbs were subtype-specific. Twenty (24%) of the 84 mAbs recognized the common HA epitopes shared by 2009 pandemic H1N1, seasonal A1 (H1N1), and A3 (H3N2) influenza viruses. Twenty-five of the 84 clones recognized the common HA epitopes shared by the 2009 pandemic H1N1, seasonal A1 (H1N1) and A3 (H3N2) human influenza viruses, and H5N1 and H9N2 avian influenza viruses. We found that of the 16 (19%) clones of the 84 mAbs panel that were cross-reactive with human respiratory pathogens, 15 were made using the HA of the seasonal A1 (H1N1) virus and 1 was made using the HA of the 2009 pandemic H1N1 influenza virus. Immunohistochemical analysis of the tissue microarray (TMA) showed that 4 of the 84 mAb clones cross-reacted with human tissue (brain and pancreas). Our results indicated that the influenza virus HA antigenic epitopes not only induce type-, subtype-, and strain-specific monoclonal antibodies against influenza A virus but also cross-reactive monoclonal antibodies against human tissues. Further investigations of these cross-reactive (heterophilic) epitopes may significantly improve our understanding of viral antigenic variation, epidemics, pathophysiologic mechanisms, and adverse effects of influenza vaccines.

Indexed as

AnimalsAntibodies, MonoclonalCells, CulturedCross ReactionsEpitope MappingHemagglutinin Glycoproteins, Influenza VirusHumansImmunodominant EpitopesInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza A Virus, H5N1 SubtypeInfluenza A Virus, H9N2 SubtypeInfluenza, HumanInfluenza VaccinesMiceTissue Array AnalysisAntibodies, MonoclonalH1N1 virus hemagglutininHemagglutinin Glycoproteins, Influenza VirusImmunodominant EpitopesInfluenza VaccinesH1N1HA proteinHuman tissues, Heterophilic antigen epitopesInfluenza virus

Identifiers

PMID25708705
PMCPMC7124281
OpenAlexW2077233112

What OpenQuestion holds

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Registered trials

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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.