Evidence map›Paper›PMID 33076544›Full record

ReviewToxins2020

Immunotoxin Screening System: A Rapid and Direct Approach to Obtain Functional Antibodies with Internalization Capacities.

Shusei Hamamichi, Takeshi Fukuhara, Nobutaka Hattori

Open access · goldAbstract readReview
In one paragraph

Review in Toxins, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. 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

3 authors at 2 institutions in 1 country.

Shusei HamamichiResearch Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0003-4613-0815
Takeshi FukuharaDepartment of Neurology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0003-2950-9516
Nobutaka HattoriDepartment of Neurology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0002-2034-2556
RIKEN Center for Brain Science · JPJuntendo University · JP

Funding

Japan Agency for Medical Research and Development JP19cm0106231s0102Japan Agency for Medical Research and Development JP19dm0107156h0001Japan Society for the Promotion of Science 16K07184Japan Society for the Promotion of Science 18K07657Japan Society for the Promotion of Science 19K07831
6 · The paper itself

Abstract

Toxins, while harmful and potentially lethal, have been engineered to develop potent therapeutics including cytotoxins and immunotoxins (ITs), which are modalities with highly selective targeting capabilities. Currently, three cytotoxins and IT are FDA-approved for treatment of multiple forms of hematological cancer, and additional ITs are tested in the clinical trials or at the preclinical level. For next generation of ITs, as well as antibody-mediated drug delivery systems, specific targeting by monoclonal antibodies is critical to enhance efficacies and reduce side effects, and this methodological field remains open to discover potent therapeutic monoclonal antibodies. Here, we describe our application of engineered toxin termed a cell-based IT screening system. This unique screening strategy offers the following advantages: (1) identification of monoclonal antibodies that recognize cell-surface molecules, (2) selection of the antibodies that are internalized into the cells, (3) selection of the antibodies that induce cytotoxicity since they are linked with toxins, and (4) determination of state-specific activities of the antibodies by differential screening under multiple experimental conditions. Since the functional monoclonal antibodies with internalization capacities have been identified successfully, we have pursued their subsequent modifications beyond antibody drug conjugates, resulting in development of immunoliposomes. Collectively, this screening system by using engineered toxin is a versatile platform, which enables straight-forward and rapid selection for discovery of novel functional antibodies.

Indexed as

High-Throughput Screening AssaysAnimalsAntibodies, MonoclonalAntibody SpecificityBacterial ToxinsBiological TransportCell MembraneCytotoxicity, ImmunologicDiphtheria ToxinExotoxinsHumansImmunoconjugatesImmunotoxinsInterleukin-2LiposomesRecombinant Fusion ProteinsAntibodies, MonoclonalBacterial Toxinsdenileukin diftitoxDiphtheria ToxinExotoxinsImmunoconjugatesimmunotoxin HA22ImmunotoxinsInterleukin-2LiposomesRecombinant Fusion Proteinstagraxofuspantibody drug conjugatediphtheria toxindrug deliveryDT3Cimmunoliposomeimmunotoxinmonoclonal antibody

Identifiers

PMID33076544
PMCPMC7602748
OpenAlexW3092847603

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.