Evidence map›Paper›PMID 32518090›Full record

ArticleJournal for immunotherapy of cancer2020

Restoration of antitumor immunity through anti-MICA antibodies elicited with a chimeric protein.

Nicolas Torres, María Victoria Regge, Florencia Secchiari, Adrián David Friedrich, Raúl Germán Spallanzani, Ximena Lucía Raffo Iraolagoitia, Sol Yanel Núñez, Jessica Mariel Sierra, Andrea Ziblat, María Cecilia Santilli and 12 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.2field-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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Observational
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. 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

22 authors at 5 institutions in 3 countries.

Nicolas TorresLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
María Victoria ReggeLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Florencia SecchiariLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Adrián David FriedrichLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Raúl Germán SpallanzaniLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Ximena Lucía Raffo IraolagoitiaLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Sol Yanel NúñezLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Jessica Mariel SierraLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Andrea ZiblatLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
María Cecilia SantilliLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Nicolás GilioLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Evangelina AlmadaLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Constanza LaucheInmunova, Buenos Aires, Argentina.
Romina PardoInmunova, Buenos Aires, Argentina.
Carolina Inés DomaicaLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Mercedes Beatriz FuertesLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina.
Kevin Patrick MadaussTrust in Science, Global Health R&D, GlaxoSmithKline, Collegeville, PA, United States.
Kenneth W HanceOncology, GlaxoSmithKline, Collegeville, PA, United States.
Israel S GlogerTrust in Science, Global Health R&D, GlaxoSmithKline, Stevenage, United Kingdom.
Vanesa ZylbermanInmunova, Buenos Aires, Argentina.
Fernando Alberto GoldbaumInmunova, Buenos Aires, Argentina.
Norberto Walter ZwirnerLaboratorio de Fisiopatología de la Inmunidad Innata, Instituto de Biologia y Medicina Experimental, Buenos Aires, Argentina nzwirner@ibyme.conicet.gov.ar.ORCID 0000-0001-7098-359X
Experimental Medicine and Biology Institute · ARGlaxoSmithKline (United States) · USFundación Instituto Leloir · ARGlaxoSmithKline (United Kingdom) · GBUniversidad de Buenos Aires · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNatural killer and cytotoxic CD8

methodsWe generated a highly immunogenic chimeric protein (BLS-MICA) consisting of human MICA fused to the lumazine synthase from

resultsImmunization with BLS-MICA and administration of anti-MICA pAb elicited by BLS-MICA significantly delayed the growth of MICA-expressing mouse tumors but not of control tumors. The therapeutic effect of immunization with BLS-MICA included scavenging of sMICA and the anti-MICA Ab-mediated ADCC, promoting heightened intratumoral M1/proinflammatory macrophage and antigen-experienced CD8

conclusionsImmunization with the chimeric protein BLS-MICA constitutes a useful way to actively induce therapeutic anti-MICA pAb that resulted in a reprogramming of the antitumor immune response towards an antitumoral/proinflammatory phenotype. Hence, the BLS-MICA chimeric protein constitutes a novel antitumor vaccine of potential application in patients with MICA-expressing tumors.

Indexed as

AnimalsAntibodies, MonoclonalAntibody-Dependent Cell CytotoxicityBrucellaFemaleHistocompatibility Antigens Class ILymphomaMaleMiceMice, Inbred C57BLMultienzyme ComplexesNK Cell Lectin-Like Receptor Subfamily KRecombinant Fusion ProteinsTumor Cells, CulturedUrinary Bladder Neoplasms6,7-dimethyl-8-ribityllumazine synthaseAntibodies, MonoclonalHistocompatibility Antigens Class IMHC class I-related chain AMultienzyme ComplexesNK Cell Lectin-Like Receptor Subfamily KRecombinant Fusion Proteinsimmunology

Identifiers

PMID32518090
PMCPMC7282397
OpenAlexW3033899855

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.