Evidence map›Paper›PMID 37467717›Full record

ArticleCell reports. Medicine2023

A target discovery pipeline identified ILT3 as a target for immunotherapy of multiple myeloma.

Francesco Di Meo, Anjushree Iyer, Keith Akama, Rujin Cheng, Christina Yu, Annamaria Cesarano, Noriyoshi Kurihara, Hirofumi Tenshin, Arafat Aljoufi, Silvia Marino and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
7.6field-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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Memory matters: T cell phenotype shapes CAR T cell fate.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  4. Review
  5. Review
  6. Review
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  8. Article
  9. Review
  10. Mapping the cancer surface proteome in search of target antigens for immunotherapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. LILRB4 on multiple myeloma cells promotes bone lesion by p-SHP2/NF-κB/RELT signal pathway.Journal of experimental & clinical cancer research : CR · 2024
    Article
  16. Review
  17. Shifting gears with CAR T cells for autoimmune diseases.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  18. Article
  19. Review
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

20 authors at 5 institutions in 2 countries.

Francesco Di MeoDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Blood and Marrow Transplant and Cellular Immunotherapy, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Anjushree IyerNGM Biopharmaceuticals, San Francisco, CA, USA.
Keith AkamaNGM Biopharmaceuticals, San Francisco, CA, USA.
Rujin ChengNGM Biopharmaceuticals, San Francisco, CA, USA.
Christina YuDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Annamaria CesaranoDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Blood and Marrow Transplant and Cellular Immunotherapy, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Noriyoshi KuriharaDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Hirofumi TenshinDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Arafat AljoufiDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, USA.
Silvia MarinoDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Rajesh K SoniProteomics and Macromolecular Crystallography Shared Resource, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Julie RodaNGM Biopharmaceuticals, San Francisco, CA, USA.
James SissonsNGM Biopharmaceuticals, San Francisco, CA, USA.
Ly P VuBritish Columbia Cancer Center, Vancouver, BC, Canada.
Monica GuzmanWeill Cornell Medical College, New York, NY, USA.
Kun HuangDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Tamara LaskowskiLonza Personalized Medicine, Basel, Switzerland.
Hal E BroxmeyerDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, USA.
David G RoodmanDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Fabiana PernaDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Blood and Marrow Transplant and Cellular Immunotherapy, H. Lee Moffitt Cancer Center, Tampa, FL, USA; Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: fabiana.perna@moffitt.org.
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineColumbia University Irving Medical Center · USCornell University · USLonza (Switzerland) · CH

Funding

Identifying cell surface targets for innovative immunotherapy of Multiple MyelomaR37CA276939 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI Fabiana Perna · 2024 to 2026
$1.7M
NCI NIH HHS R37 CA276939
6 · The paper itself

Abstract

Multiple myeloma (MM) is an incurable malignancy of plasma cells. To identify targets for MM immunotherapy, we develop an integrated pipeline based on mass spectrometry analysis of seven MM cell lines and RNA sequencing (RNA-seq) from 900+ patients. Starting from 4,000+ candidates, we identify the most highly expressed cell surface proteins. We annotate candidate protein expression in many healthy tissues and validate the expression of promising targets in 30+ patient samples with relapsed/refractory MM, as well as in primary healthy hematopoietic stem cells and T cells by flow cytometry. Six candidates (ILT3, SEMA4A, CCR1, LRRC8D, FCRL3, IL12RB1) and B cell maturation antigen (BCMA) present the most favorable profile in malignant and healthy cells. We develop a bispecific T cell engager targeting ILT3 that shows potent killing effects in vitro and decreased tumor burden and prolonged mice survival in vivo, suggesting therapeutic relevance. Our study uncovers MM-associated antigens that hold great promise for immune-based therapies of MM.

Indexed as

Multiple MyelomaAnimalsImmunotherapyMicePlasma CellsT-LymphocytesBCMAbi-specific T cell engagerCCR1FCRL3IL12RB1ILT3Immune-TargetFinder pipelineimmunotherapyLRRC8DMass-Spectrometrymultiple myelomaprimary patient samplesSEMA4Atarget antigensTarget discovery strategyvalidation

Identifiers

PMID37467717
PMCPMC10394163
OpenAlexW4384700492

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.