Evidence map›Paper›PMID 26261057›Full record

ArticlemAbs2015

Characterization of anti-CD20 monoclonal antibody produced by transgenic silkworms (Bombyx mori).

Minoru Tada, Ken-ichiro Tatematsu, Akiko Ishii-Watabe, Akira Harazono, Daisuke Takakura, Noritaka Hashii, Hideki Sezutsu, Nana Kawasaki

Open access · goldAbstract read
In one paragraph

Article in mAbs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 45 citations in OpenAlex.

  1. Application of Transgenic Silk Fibroin to Biomaterials.Biotechnology and bioengineering · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. An update of KAIKObase, the silkworm genome database.Database : the journal of biological databases and curation · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Development of an LC-MS/MS peptide mapping protocol for the NISTmAb.Analytical and bioanalytical chemistry · 2018
    Article
  19. Article
  20. 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

8 authors at 2 institutions in 2 countries.

Minoru Tadaa Division of Biological Chemistry and Biologicals; National Institute of Health Sciences ; Tokyo , Japan.
Ken-ichiro Tatematsub Transgenic Silkworm Research Unit; National Institute of Agrobiological Sciences ; Ibaraki , Japan.
Akiko Ishii-Watabea Division of Biological Chemistry and Biologicals; National Institute of Health Sciences ; Tokyo , Japan.
Akira Harazonoa Division of Biological Chemistry and Biologicals; National Institute of Health Sciences ; Tokyo , Japan.
Daisuke Takakuraa Division of Biological Chemistry and Biologicals; National Institute of Health Sciences ; Tokyo , Japan.
Noritaka Hashiia Division of Biological Chemistry and Biologicals; National Institute of Health Sciences ; Tokyo , Japan.
Hideki Sezutsub Transgenic Silkworm Research Unit; National Institute of Agrobiological Sciences ; Ibaraki , Japan.
Nana Kawasakia Division of Biological Chemistry and Biologicals; National Institute of Health Sciences ; Tokyo , Japan.
Biologicals (Czechia) · CZInstitute of Agrobiological Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In response to the successful use of monoclonal antibodies (mAbs) in the treatment of various diseases, systems for expressing recombinant mAbs using transgenic animals or plants have been widely developed. The silkworm (Bombyx mori) is a highly domesticated insect that has recently been used for the production of recombinant proteins. Because of their cost-effective breeding and relatively easy production scale-up, transgenic silkworms show great promise as a novel production system for mAbs. In this study, we established a transgenic silkworm stably expressing a human-mouse chimeric anti-CD20 mAb having the same amino acid sequence as rituximab, and compared its characteristics with rituximab produced by Chinese hamster ovary (CHO) cells (MabThera®). The anti-CD20 mAb produced in the transgenic silkworm showed a similar antigen-binding property, but stronger antibody-dependent cell-mediated cytotoxicity (ADCC) and weaker complement-dependent cytotoxicity (CDC) compared to MabThera. Post-translational modification analysis was performed by peptide mapping using liquid chromatography/mass spectrometry. There was a significant difference in the N-glycosylation profile between the CHO- and the silkworm-derived mAbs, but not in other post-translational modifications including oxidation and deamidation. The mass spectra of the N-glycosylated peptide revealed that the observed biological properties were attributable to the characteristic N-glycan structures of the anti-CD20 mAbs produced in the transgenic silkworms, i.e., the lack of the core-fucose and galactose at the non-reducing terminal. These results suggest that the transgenic silkworm may be a promising expression system for the tumor-targeting mAbs with higher ADCC activity.

Indexed as

AnimalsAnimals, Genetically ModifiedAntibodies, MonoclonalAntibody-Dependent Cell CytotoxicityAntibody SpecificityAntigens, CD20BombyxCell Line, TumorCHO CellsChromatography, LiquidComplement System ProteinsCricetinaeCricetulusCytotoxicity, ImmunologicGlycosylationHumansAntibodies, MonoclonalAntigens, CD20Complement System ProteinsRecombinant ProteinsRituximabADCCmonoclonal antibodyN-glycosylationrituximabtransgenic silkworm

Identifiers

PMID26261057
PMCPMC4966511
OpenAlexW2112335360

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.