Evidence map›Paper›PMID 26282003›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Antibody response to HER2 extracellular domain and subdomains in mouse following DNA immunization.

Fateme Sadri-Ardalani, Mahdi Shabani, Mohammad Mehdi Amiri, Motahareh Bahadori, Shaghayegh Emami, Ali Reza Sarrafzadeh, Farzaneh Noutash-Haghighat, Mahmood Jeddi-Tehrani, Fazel Shokri

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Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. 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
0.5field-weighted citation impact, top 31% 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. HER2-Positive Breast Cancer Immunotherapy: A Focus on Vaccine Development.Archivum immunologiae et therapiae experimentalis · 2020
    Review
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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 2 institutions in 1 country.

Fateme Sadri-ArdalaniMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Mahdi ShabaniMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran. m.shabani@avicenna.ac.ir.
Mohammad Mehdi AmiriMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Motahareh BahadoriMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Shaghayegh EmamiMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Ali Reza SarrafzadehDepartment of Pathology, Khatam Al Anbia Hospital, Tehran, Iran.
Farzaneh Noutash-HaghighatMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Mahmood Jeddi-TehraniMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Fazel ShokriMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran. fshokri@tums.ac.ir.
Academic Center for Education, Culture and Research · IRKhatam University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human epidermal growth factor receptor 2 (HER2) is overexpressed in 15-20 % of breast cancer patients and is an appropriate target for immunotherapy in these patients. Monoclonal antibodies (mAbs) specific to HER2 are currently applied to treat breast cancer patients with HER2 overexpression. Active immunization with HER2 DNA or protein has been considered as a suitable alternative. The aim of this study is to evaluate anti-HER2 antibody response in serum of mice immunized with DNA constructs containing full extracellular domain (fECD) or subdomains of human HER2. Four extracellular subdomains and also fECD of HER2 were cloned into pCMV6-Neo vector. Different groups of Balb/C mice were immunized with HER2 DNA constructs and boosted with HER2 recombinant protein. The anti-HER2 antibody was subsequently determined by ELISA, flow cytometry, and immunohistochemistry. Anti-HER2 antibody was detected only in serum of mice immunized with fECD DNA. None of HER2 extracellular subdomains induced appreciable levels of anti-HER2 antibody. However, boosting with fECD or extracellular subdomain III (DIII) recombinant protein resulted in enhanced anti-HER2 fECD as well as anti-HER2 subdomain antibody responses. In this regard, almost all (99 %) of HER2-overexpressing BT474 cells could be detected by serum antibody from mice immunized with HER2 subdomain DNA and boosted with recombinant HER2 protein by flow cytometry. Similarly, serum of mice immunized with DIII DNA construct and boosted with recombinant DIII protein could also recognize these cells, but to a lesser extent (50 %). Our findings suggest that combination of HER2 DNA and protein immunization could effectively induce anti-HER2 antibody response in Balb/C mice.

Indexed as

Antibody FormationAnimalsAntibodies, MonoclonalBreast NeoplasmsCancer VaccinesDNA PrimersEnzyme-Linked Immunosorbent AssayErb-b2 Receptor Tyrosine KinasesFemaleFlow CytometryGenetic VectorsHumansImmunohistochemistryImmunotherapyMiceMice, Inbred BALB CAntibodies, MonoclonalCancer VaccinesDNA PrimersERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesRecombinant ProteinsVaccines, DNABreast cancerDNA immunizationExtracellular domainsHER2ImmunotherapyRecombinant protein

Identifiers

PMID26282003
OpenAlexW1177799805

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.