Evidence map›Paper›PMID 25941618›Full record

ReviewOncoimmunology2014

Tumor antigen-targeting monoclonal antibody-based immunotherapy: Orchestrating combined strategies for the development of long-term antitumor immunity.

Henri-Alexandre Michaud, Jean-François Eliaou, Virginie Lafont, Nathalie Bonnefoy, Laurent Gros

Open access · goldAbstract readReview
In one paragraph

Review in Oncoimmunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 58 citations in OpenAlex.

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  19. Bioactive Nanoparticles for Cancer Immunotherapy.International journal of molecular sciences · 2018
    Review
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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

5 authors at 3 institutions in 1 country.

Henri-Alexandre MichaudInstitut de Recherche en Cancérologie de Montpellier; Inserm U896 ; Institut Régional de Lutte contre le Cancer (ICM); Université Montpellier 1 ; Montpellier Cedex, France.
Jean-François EliaouInstitut de Recherche en Cancérologie de Montpellier; Inserm U896 ; Institut Régional de Lutte contre le Cancer (ICM); Université Montpellier 1 ; Montpellier Cedex, France ; Département d'Immunologie; CHRU Montpellier and Faculté de Médecine; Université Montpellier I ; Montpellier Cedex, France.
Virginie LafontInstitut de Recherche en Cancérologie de Montpellier; Inserm U896 ; Institut Régional de Lutte contre le Cancer (ICM); Université Montpellier 1 ; Montpellier Cedex, France.
Nathalie BonnefoyInstitut de Recherche en Cancérologie de Montpellier; Inserm U896 ; Institut Régional de Lutte contre le Cancer (ICM); Université Montpellier 1 ; Montpellier Cedex, France ; co-senior authors.
Laurent GrosInstitut de Recherche en Cancérologie de Montpellier; Inserm U896 ; Institut Régional de Lutte contre le Cancer (ICM); Université Montpellier 1 ; Montpellier Cedex, France ; co-senior authors.
Institut de Recherche en Cancérologie de Montpellier · FRInserm · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor antigen (TA)-targeting monoclonal antibody (mAb)-based treatments are considered to be one of the most successful strategies in cancer therapy. Besides targeting TAs and inducing tumor cell death, such antibodies interact with immune cells through Fc-dependent mechanisms to induce adaptive memory immune responses. However, multiple inhibitory/immunosuppressive pathways can be induced by tumor cells to limit the establishment of an efficient antitumor response and consequently a sustained clinical response to TA-targeting mAbs. Here, we provide an overview on how TA-targeting mAbs in combination with conventional cancer therapies and/or inhibitors of key immunosuppressive pathways might represent promising approaches to achieve long-term tumor control.

Indexed as

ADCC, antibody-dependent cell cytotoxicityADCP, antibody-dependent cell phagocytosisB-NHL, B-cell non-Hodgkin's lymphomaCDC, complement-dependent cytotoxicitycombined therapiesCTLA4, cytotoxic T-lymphocyte-associated protein 4DC, dendritic cellFcRn, neonatal Fc receptorFDA, food and drug administrationHMGB1, high-mobility group box 1ICD, immunologic cell deathIDO, indoleamine 2, 3-dioxygenaseIFNγ, interferon γimmunomodulationimmunosuppressive pathwaysmAb, monoclonal antibodyMDSC, myeloid-derived suppressor cellNK, natural killerPD-1, programmed cell death 1TA-targeting mAbsTA, tumor antigenTreg, regulatory T cellvaccine-like effects

Identifiers

PMID25941618
PMCPMC4292589
OpenAlexW1984778395

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.