Evidence map›Paper›PMID 25072059›Full record

ArticlemAbs

Highly potent anti-CD20-RLI immunocytokine targeting established human B lymphoma in SCID mouse.

Marie Vincent, Géraldine Teppaz, Laurie Lajoie, Véronique Solé, Anne Bessard, Mike Maillasson, Séverine Loisel, David Béchard, Béatrice Clémenceau, Gilles Thibault and 3 more

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Utilizing Immunocytokines for Cancer Therapy.Antibodies (Basel, Switzerland) · 2021
    Review
  12. Review
  13. Observational
  14. Review
  15. Review
  16. Review
  17. Cytokines in the Treatment of Cancer.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2019
    Review
  18. Cytokines in Cancer Immunotherapy.Cold Spring Harbor perspectives in biology · 2018
    Review
  19. IL-15 enhanced antibody-dependent cellular cytotoxicity mediated by NK cells and macrophages.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  20. Engineering Platforms for T Cell Modulation.International review of cell and molecular biology · 2018
    Review
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

13 authors at 5 institutions in 2 countries.

Marie Vincent
Géraldine Teppaz
Laurie Lajoie
Véronique Solé
Anne Bessard
Mike Maillasson
Séverine Loisel
David Béchard
Béatrice Clémenceau
Gilles Thibault
Laure Garrigue-Antar
Yannick Jacques
Agnès Quéméner
Centre National de la Recherche Scientifique · FRNantes Université · FRInserm · FRBridge Pharma (United States) · USUniversité Européenne de Bretagne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rituximab (RTX), a chimeric IgG1 monoclonal antibody directed against the CD20 antigen, has revolutionized the treatment of B-cell malignancies. Nevertheless, the relapsed/refractory rates are still high. One strategy to increase the clinical effectiveness of RTX is based on antibody-cytokine fusion protein (immunocytokine; ICK) vectorizing together at the tumor site the antibody effector activities and the cytokine co-signal required for the generation of cytotoxic cellular immunity. Such ICKs linking various antibody formats to interleukin (IL)-2 are currently being investigated in clinical trials and have shown promising results in cancer therapies. IL-15, a structurally-related cytokine, is now considered as having a better potential than IL-2 in antitumor immunotherapeutic strategies. We have previously engineered the fusion protein RLI, linking a soluble form of human IL-15Rα-sushi+ domain to human IL-15. Compared with IL-15, RLI displayed better biological activities in vitro and higher antitumor effects in vivo in murine and human cancer models. In this study, we investigated the advantages of fusing RLI to RTX. Anti-CD20-RLI kept its binding capacity to CD20, CD16 and IL-15 receptor and therefore fully retained both antibody effector functions (ADCC and CDC), and the cytokine potential of RLI. In a severe combined immunodeficiency (SCID) mouse model of disseminated residual lymphoma, anti-CD20-RLI was found to induce long-term survival of 90% of mice up to at least 120 days whereas RLI and RTX, alone or in combination, just delayed the disease onset (100% of death at 28, 40 and 51 days respectively). These findings suggest that such ICK could improve the clinical efficacy of RTX, particularly in patients with refractory B-cell lymphoma.

Indexed as

AnimalsAntibodies, Monoclonal, Murine-DerivedAntineoplastic AgentsCHO CellsCricetinaeCricetulusFemaleHumansImmunoconjugatesInterleukin-2Lymphoma, B-CellMaleMiceMice, SCIDRecombinant Fusion ProteinsRituximabAntibodies, Monoclonal, Murine-DerivedAntineoplastic AgentsIL-15Ralpha-sushi domain-linker-IL-15 fusion proteinIL2 protein, humanImmunoconjugatesInterleukin-2Recombinant Fusion ProteinsRituximab

Identifiers

PMID25072059
PMCPMC4171006
OpenAlexW2004976004

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.