Evidence map›Paper›PMID 27530750›Full record

ReviewEmerging microbes & infections2016

Converting monoclonal antibody-based immunotherapies from passive to active: bringing immune complexes into play.

Jennifer Lambour, Mar Naranjo-Gomez, Marc Piechaczyk, Mireia Pelegrin

Open access · goldAbstract readReview
In one paragraph

Review in Emerging microbes & infections, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 51 citations in OpenAlex.

  1. Trial
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  9. OMIP-085: Cattle B-cell phenotyping by an 8-color panel.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2023
    Article
  10. Review
  11. Review
  12. Article
  13. Article
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  15. Immune Prophylaxis and Therapy for Human Cytomegalovirus Infection.International journal of molecular sciences · 2021
    Review
  16. Review
  17. An update on antiviral antibody-based biopharmaceuticals.International immunopharmacology · 2020
    Review
  18. Review
  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

4 authors at 1 institution in 1 country.

Jennifer Lambour'Equipe Labellisée par la Ligue Contre le Cancer' - Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, 34293 Montpellier Cedex 5, France; Université de Montpellier, 34090 Montpellier, France.
Mar Naranjo-Gomez'Equipe Labellisée par la Ligue Contre le Cancer' - Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, 34293 Montpellier Cedex 5, France; Université de Montpellier, 34090 Montpellier, France.
Marc Piechaczyk'Equipe Labellisée par la Ligue Contre le Cancer' - Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, 34293 Montpellier Cedex 5, France; Université de Montpellier, 34090 Montpellier, France.
Mireia Pelegrin'Equipe Labellisée par la Ligue Contre le Cancer' - Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, 34293 Montpellier Cedex 5, France; Université de Montpellier, 34090 Montpellier, France.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal antibodies (mAbs), which currently constitute the main class of biotherapeutics, are now recognized as major medical tools that are increasingly being considered to fight severe viral infections. Indeed, the number of antiviral mAbs developed in recent years has grown exponentially. Although their direct effects on viral blunting have been studied in detail, their potential immunomodulatory actions have been overlooked until recently. The ability of antiviral mAbs to modulate antiviral immune responses in infected organisms has recently been revealed. More specifically, upon recognition of their cognate antigens, mAbs form immune complexes (ICs) that can be recognized by the Fc receptors expressed on different immune cells of infected individuals. This binding may be followed by the modulation of the host immune responses. Harnessing this immunomodulatory property may facilitate improvements in the therapeutic potential of antiviral mAbs. This review focuses on the role of ICs formed with different viral determinants and mAbs in the induction of antiviral immune responses in the context of both passive immunotherapies and vaccination strategies. Potential deleterious effects of ICs on the host immune response are also discussed.

Indexed as

Immunization, PassiveImmunotherapy, ActiveAnimalsAntibodies, MonoclonalAntibodies, ViralAntigen-Antibody ComplexAntigens, ViralAntiviral AgentsDisease Models, AnimalHumansImmunoglobulin Fc FragmentsImmunologic FactorsImmunomodulationVaccinationVirus DiseasesAntibodies, MonoclonalAntibodies, ViralAntigen-Antibody ComplexAntigens, ViralAntiviral AgentsImmunoglobulin Fc FragmentsImmunologic Factors

Identifiers

PMID27530750
PMCPMC5034104
OpenAlexW2516118470

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.