Evidence map›Paper›PMID 31144209›Full record

ReviewClinical reviews in allergy & immunology2020

Complement System: a Neglected Pathway in Immunotherapy.

Anne Bordron, Cristina Bagacean, Adrian Tempescul, Christian Berthou, Eléonore Bettacchioli, Sophie Hillion, Yves Renaudineau

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical reviews in allergy & immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. gC1qR: A New Target for Cancer Immunotherapy.Frontiers in immunology · 2023
    Review
  14. Article
  15. Review
  16. Isotype selection for antibody-based cancer therapy.Clinical and experimental immunology · 2021
    Review
  17. Review
  18. Review
  19. Inflammation in Hypertension.The Canadian journal of cardiology · 2020
    Review
  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

7 authors at 2 institutions in 1 country.

Anne BordronInserm UMR1227, B lymphocytes and autoimmunity, University of Brest, Brest, France.
Cristina BagaceanInserm UMR1227, B lymphocytes and autoimmunity, University of Brest, Brest, France.
Adrian TempesculInserm UMR1227, B lymphocytes and autoimmunity, University of Brest, Brest, France.
Christian BerthouInserm UMR1227, B lymphocytes and autoimmunity, University of Brest, Brest, France.
Eléonore BettacchioliLaboratory of Immunology and Immunotherapy, CHU de Brest, Brest, France.
Sophie HillionInserm UMR1227, B lymphocytes and autoimmunity, University of Brest, Brest, France.
Yves RenaudineauInserm UMR1227, B lymphocytes and autoimmunity, University of Brest, Brest, France. yves.renaudineau@univ-brest.fr.ORCID http://orcid.org/0000-0001-5098-5002
Inserm · FRCentre Hospitalier Régional Universitaire de Brest · FR

Funding

Brest University Hospital INNOVEO donation fund Careco
6 · The paper itself

Abstract

Approved for the treatment of autoimmune diseases, hematological malignancies, and solid cancers, several monoclonal antibodies (mAb) make use of complement in their mechanism of action. Such an assessment is based on comprehensive investigations that used mouse models, in vitro studies, and analyses from patients at initiation (basal level to highlight deficiencies) and after treatment initiation (mAb impact on complement), which have further provided key insights into the importance of the complement activation and/or complement deficiencies in mAb activity. Accordingly, new approaches can now be developed with the final objective of increasing the clinical efficacy of mAb. These improvements include (i) the concurrent administration of fresh frozen plasma during mAb therapy; (ii) mAb modifications such as immunoglobulin G subclass switching, Fc mutation, or IgG hexamerization to improve the fixation and activation of C1q; (iii) optimization of the target recognition to induce a higher complement-dependent cytotoxicity (CDC) and/or complement-dependant cellular cytotoxicity (CDCC); and (iv) the control of soluble and cellular complement inhibitors.

Indexed as

AnimalsAntibodies, MonoclonalBiomarkersComplement ActivationComplement Pathway, AlternativeComplement Pathway, ClassicalComplement System ProteinsHumansImmunologic FactorsImmunotherapyTreatment OutcomeAntibodies, MonoclonalBiomarkersComplement System ProteinsImmunologic FactorsAutoimmunity cancerComplementMonoclonal antibody

Identifiers

PMID31144209
OpenAlexW2947171827

What OpenQuestion holds

Textmetadata
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.