Evidence map›Paper›PMID 28581886›Full record

ReviewmAbs2018

Enhanced immunization techniques to obtain highly specific monoclonal antibodies.

Rodrigo de Almeida, Cecília Naomi Nakamura, Marina de Lima Fontes, Elenice Deffune, Sérgio Luis Felisbino, Ramon Kaneno, Wagner José Fávaro, Athanase Billis, Marcel Otavio Cerri, Ana Marisa Fusco-Almeida and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in mAbs, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. 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

12 authors at 2 institutions in 1 country.

Rodrigo de Almeidaa Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara, Proteomics Center, Monoclonal Antibody Lab. , Araraquara , Brazil.
Cecília Naomi Nakamuraa Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara, Proteomics Center, Monoclonal Antibody Lab. , Araraquara , Brazil.
Marina de Lima Fontesa Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara, Proteomics Center, Monoclonal Antibody Lab. , Araraquara , Brazil.
Elenice Deffuneb Universidade Estadual Paulista (Unesp), Faculdade de Medicina, Botucatu, Blood Transfusion Center, Cell Engineering Lab. , Botucatu , Brazil.
Sérgio Luis Felisbinoc Universidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatu , Department of Morphology, Extracellular Matrix Lab ., Botucatu , Brazil.
Ramon Kanenod Universidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatu , Department of Microbiology and Immunology, Tumor Immunology Lab ., Botucatu , Brazil.
Wagner José Fávaroe Univ Campinas - UNICAMP, Biology Institute , Department of Structural and Functional Biology, Immunotherapy Lab ., Campinas , SP , Brazil.
Athanase Billisf Univ Estadual Campinas - UNICAMP, School of Medicine , Department of Pathology, Uropathology Lab. , Campinas , SP , Brazil.
Marcel Otavio Cerrig Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara , Department of Bioprocess and Biotechnology , Araraquara , Brazil.
Ana Marisa Fusco-Almeidaa Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara, Proteomics Center, Monoclonal Antibody Lab. , Araraquara , Brazil.
Maria José Mendes Gianninia Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara, Proteomics Center, Monoclonal Antibody Lab. , Araraquara , Brazil.
Andrei Moroza Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara, Proteomics Center, Monoclonal Antibody Lab. , Araraquara , Brazil.
Universidade Estadual Paulista (Unesp) · BRUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite fast advances in genomics and proteomics, monoclonal antibodies (mAbs) are still a valuable tool for areas such as the evolution of basic research in stem cells and cancer, for immunophenotyping cell populations, diagnosing and prognosis of diseases, and for immunotherapy. To summarize different subtractive immunization approaches successfully used for the production of highly specific antibodies, we identified scientific articles in NCBI PubMed using the following search terms: subtractive immunization, monoclonal antibody, tolerization, neonatal, high-zone tolerance, masking immunization. Patent records were also consulted. From the list of results, we included all available reports, from 1985 to present, that used any enhanced immunization technique to produce either polyclonal or monoclonal antibodies. Our examination yielded direct evidence that these enhanced immunization techniques are efficient in obtaining specific antibodies to rare epitopes, with different applications, such as to identify food contaminants or tumor cells.

Indexed as

Antibody SpecificityAnimalsAnimals, NewbornAntibodies, MonoclonalAntigensHumansImmune ToleranceImmunizationImmunization ScheduleImmunodominant EpitopesAntibodies, MonoclonalAntigensImmunodominant EpitopesCyclophosphamidehigh-zone toleranceimmunogenmonoclonal antibodymultiple tolerization subtractive immunizationneonatal tolerizationsubtractive immunizationtolerogen

Identifiers

PMID28581886
PMCPMC5800380
OpenAlexW2622800264

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.