Evidence map›Paper›PMID 24326534›Full record

ArticleBlood2014

Anti-KIR antibody enhancement of anti-lymphoma activity of natural killer cells as monotherapy and in combination with anti-CD20 antibodies.

Holbrook E Kohrt, Ariane Thielens, Aurelien Marabelle, Idit Sagiv-Barfi, Caroline Sola, Fabien Chanuc, Nicolas Fuseri, Cécile Bonnafous, Debra Czerwinski, Amanda Rajapaksa and 7 more

Abstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 184 papers.

0numbers the graph read from it
0cells of the map it votes in
184citing papers in PubMed
12.2field-weighted citation impact, top 1% 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

184 citing papers in PubMed, 274 citations in OpenAlex.

  1. Trial
  2. Haploidentical Natural Killer Cells Infused before Allogeneic Stem Cell Transplantation for Myeloid Malignancies: A Phase I Trial.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2016
    Trial
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Emerging combined CAR-NK cell therapies in cancer treatment: Finding a dancing partner.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Reprogramming natural killer cells for cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  18. Article
  19. Article
  20. Review

124 more citing papers are in PubMed but not listed here.

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

17 authors at 4 institutions in 2 countries.

Holbrook E KohrtDepartment of Medicine, Division of Oncology, Stanford University, Stanford, CA;
Ariane Thielens
Aurelien Marabelle
Idit Sagiv-Barfi
Caroline Sola
Fabien Chanuc
Nicolas Fuseri
Cécile Bonnafous
Debra Czerwinski
Amanda Rajapaksa
Erin Waller
Sophie Ugolini
Eric Vivier
François Romagné
Ronald Levy
Mathieu Bléry
Pascale André
Innate Pharma (France) · FRStanford University · USCentre de Recherche en Cancérologie de Lyon · FRAix-Marseille Université · FR

Funding

TRIGGERING CELL DEATH IN B CELL LYMPHOMAP01CA034233 · NCI · STANFORD UNIVERSITY · PI FELSHER, DEAN W · 1985 to 2010
$19.5M
ANTIIDIOTYPE THERAPY OF HUMAN B CELL MALIGNANCYR37CA033399 · NCI · STANFORD UNIVERSITY · PI LEVY, RONALD · 1988 to 2007
$4.5M
HUMAN ANTITUMOR THERAPY WITH MONOCLONAL ANTIBODIESR01CA033399 · NCI · STANFORD UNIVERSITY · PI LEVY, RONALD · 1985 to 1998
–
NCI NIH HHS CA33399NCI NIH HHS CA34233NCI NIH HHS P01 CA034233NCI NIH HHS R37 CA033399
6 · The paper itself

Abstract

Natural killer (NK) cells mediate antilymphoma activity by spontaneous cytotoxicity and antibody-dependent cell-mediated cytotoxicity (ADCC) when triggered by rituximab, an anti-CD20 monoclonal antibody (mAb) used to treat patients with B-cell lymphomas. The balance of inhibitory and activating signals determines the magnitude of the efficacy of NK cells by spontaneous cytotoxicity. Here, using a killer-cell immunoglobulin-like receptor (KIR) transgenic murine model, we show that blockade of the interface of inhibitory KIRs with major histocompatibility complex (MHC) class I antigens on lymphoma cells by anti-KIR antibodies prevents a tolerogenic interaction and augments NK-cell spontaneous cytotoxicity. In combination with anti-CD20 mAbs, anti-KIR treatment induces enhanced NK-cell-mediated, rituximab-dependent cytotoxicity against lymphoma in vitro and in vivo in KIR transgenic and syngeneic murine lymphoma models. These results support a therapeutic strategy of combination rituximab and KIR blockade through lirilumab, illustrating the potential efficacy of combining a tumor-targeting therapy with an NK-cell agonist, thus stimulating the postrituximab antilymphoma immune response.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntibody-Dependent Cell CytotoxicityAntigens, CD20Cell LineFemaleHistocompatibility Antigens Class IHumansKiller Cells, NaturalLymphomaMaleMiceReceptors, KIRRituximabAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, CD20Histocompatibility Antigens Class IReceptors, KIRRituximab

Identifiers

PMID24326534
PMCPMC3907754
OpenAlexW2047353087

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.