Evidence map›Paper›PMID 19553639›Full record

ArticleBlood2009

Preclinical characterization of 1-7F9, a novel human anti-KIR receptor therapeutic antibody that augments natural killer-mediated killing of tumor cells.

Francois Romagné, Pascale André, Pieter Spee, Stefan Zahn, Nicolas Anfossi, Laurent Gauthier, Marusca Capanni, Loredana Ruggeri, Don M Benson, Bradley W Blaser and 6 more

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 229 papers.

0numbers the graph read from it
0cells of the map it votes in
229citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

229 citing papers in PubMed, 389 citations in OpenAlex.

  1. Trial
  2. Checkpoint Inhibition of KIR2D with the Monoclonal Antibody IPH2101 Induces Contraction and Hyporesponsiveness of NK Cells in Patients with Myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Emerging roles of KIR2DL4 in cancer immunotherapy.Breast cancer (Tokyo, Japan) · 2025
    Review
  9. PD-1Journal of experimental & clinical cancer research : CR · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Multiple myeloma and the potential of new checkpoint inhibitors for immunotherapy.Therapeutic advances in vaccines and immunotherapy · 2024
    Review
  18. Review
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 4 countries.

Francois RomagnéInnate-Pharma SA, Marseille, France. Francois.romagne@innate-pharma.fr
Pascale André
Pieter Spee
Stefan Zahn
Nicolas Anfossi
Laurent Gauthier
Marusca Capanni
Loredana Ruggeri
Don M Benson
Bradley W Blaser
Mariella Della Chiesa
Alessandro Moretta
Eric Vivier
Michael A Caligiuri
Andrea Velardi
Nicolai Wagtmann
Innate Pharma (France) · FRNovo Nordisk (Denmark) · DKThe Ohio State University · USUniversity of Perugia · ITUniversity of Genoa · ITCentre d’Immunologie de Marseille-Luminy · FR

Funding

TWO SIGNAL REQUIREMENT FOR NATURAL KILLER IMMUNITYP01CA095426 · NCI · OHIO STATE UNIVERSITY · PI CALIGIURI, MICHAEL A · 2002 to 2016
$29.6M
Rebuilding Immunity for SurvivalP01CA100265 · NCI · DANA-FARBER CANCER INSTITUTE · PI NADLER, LEE MARSHALL · 2003 to 2005
$7.2M
IL-15--CHARACTERIZATION THROUGH EXPERIMENTAL IMMUNOLOGYR01CA068458 · NCI · ROSWELL PARK CANCER INSTITUTE · PI CALIGIURI, MICHAEL A, YU, JIANHUA · 1996 to 2019
$4.5M
NCI NIH HHS 1 PO1 CA100265NCI NIH HHS P01 CA095426NCI NIH HHS P01 CA100265NCI NIH HHS P01 CA95426-01NCI NIH HHS R01 CA068458NCI NIH HHS R01 CA68458-08
6 · The paper itself

Abstract

Inhibitory-cell killer immunoglobulin-like receptors (KIR) negatively regulate natural killer (NK) cell-mediated killing of HLA class I-expressing tumors. Lack of KIR-HLA class I interactions has been associated with potent NK-mediated antitumor efficacy and increased survival in acute myeloid leukemia (AML) patients upon haploidentical stem cell transplantation from KIR-mismatched donors. To exploit this pathway pharmacologically, we generated a fully human monoclonal antibody, 1-7F9, which cross-reacts with KIR2DL1, -2, and -3 receptors, and prevents their inhibitory signaling. The 1-7F9 monoclonal antibody augmented NK cell-mediated lysis of HLA-C-expressing tumor cells, including autologous AML blasts, but did not induce killing of normal peripheral blood mononuclear cells, suggesting a therapeutic window for preferential enhancement of NK-cell cytotoxicity against malignant target cells. Administration of 1-7F9 to KIR2DL3-transgenic mice resulted in dose-dependent rejection of HLA-Cw3-positive target cells. In an immunodeficient mouse model in which inoculation of human NK cells alone was unable to protect against lethal, autologous AML, preadministration of 1-7F9 resulted in long-term survival. These data show that 1-7F9 confers specific, stable blockade of KIR, boosting NK-mediated killing of HLA-matched AML blasts in vitro and in vivo, providing a preclinical basis for initiating phase 1 clinical trials with this candidate therapeutic antibody.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsCells, CulturedCytotoxicity, ImmunologicHumansImmunotherapyKiller Cells, NaturalMiceMice, Inbred C57BLMice, Inbred NODMice, SCIDMice, TransgenicNeoplasmsReceptors, KIRReceptors, KIR2DL1Antibodies, MonoclonalAntineoplastic AgentsKIR2DL1 protein, humanReceptors, KIRReceptors, KIR2DL1Receptors, KIR2DL2Receptors, KIR2DL3

Identifiers

PMID19553639
PMCPMC2756126
OpenAlexW2023082289

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.