Evidence map›Paper›PMID 26293646›Full record

ArticleLeukemia2016

Targeting IL-17A in multiple myeloma: a potential novel therapeutic approach in myeloma.

R H Prabhala, M Fulciniti, D Pelluru, N Rashid, A Nigroiu, P Nanjappa, C Pai, S Lee, N S Prabhala, R L Bandi and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

45 citing papers in PubMed, 74 citations in OpenAlex.

  1. Progress in Designing Cytokine Antagonist Antibodies for Cancer Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  2. Article
  3. T Cells Dysfunction in Multiple Myeloma.ImmunoTargets and therapy · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Management of Myeloma Bone Lesions.International journal of molecular sciences · 2021
    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

21 authors at 7 institutions in 2 countries.

R H PrabhalaDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
M FulcinitiDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
D PelluruDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
N RashidDepartment of Medicine, Brigham & Women's Hospital, Harvard Medical School, Boston, MA, USA.
A NigroiuDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
P NanjappaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
C PaiDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
S LeeDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
N S PrabhalaDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
R L BandiDepartment of Medicine, Brigham & Women's Hospital, Harvard Medical School, Boston, MA, USA.
R SmithDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
S B Lazo-KallanianDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
S ValetDepartment of Medicine, Massachusetts General Hospital, Boston, MA, USA.
N RajeDepartment of Medicine, Massachusetts General Hospital, Boston, MA, USA.
J S GoldDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
P G RichardsonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
J F DaleyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
K C AndersonDepartment of Medicine, Brigham & Women's Hospital, Harvard Medical School, Boston, MA, USA.
S A EttenbergNovartis Institute for Biomedical Research, Cambridge, MA, USA.
F Di PadovaNovartis Institute for Biomedical Research, Basel, Switzerland.
N C MunshiDepartment of Medicine, VA Boston Healthcare System, Harvard Medical School, Boston, MA, USA.
Dana-Farber Cancer Institute · USHarvard University · USVA Boston Healthcare System · USBrigham and Women's Hospital · USMassachusetts General Hospital · USNovartis Institutes for BioMedical ResearchNovartis (United States) · US

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
BLRD VA I01 BX001584NCI NIH HHS P01 CA155258NCI NIH HHS P50 CA100707
6 · The paper itself

Abstract

We have previously demonstrated that interleukin-17A (IL-17) producing T helper 17 cells are significantly elevated in blood and bone marrow (BM) in multiple myeloma (MM) and IL-17A promotes MM cell growth via the expression of IL-17 receptor. In this study, we evaluated anti-human IL-17A human monoclonal antibody (mAb), AIN457 in MM. We observe significant inhibition of MM cell growth by AIN457 both in the presence and the absence of BM stromal cells (BMSCs). Although IL-17A induces IL-6 production, AIN457 significantly downregulated IL-6 production and MM cell adhesion in MM-BMSC co-culture. AIN457 also significantly inhibited osteoclast cell differentiation. More importantly, in the SCIDhu model of human myeloma administration of AIN457 weekly for 4 weeks after the first detection of tumor in mice led to a significant inhibition of tumor growth and reduced bone damage compared with isotype control mice. To understand the mechanism of action of anti-IL-17A mAb, we report, here, that MM cells express IL-17A. We also observed that IL-17A knockdown inhibited MM cell growth and their ability to induce IL-6 production in co-cultures with BMSC. These pre-clinical observations suggest efficacy of AIN457 in myeloma and provide the rationale for its clinical evaluation for anti-myeloma effects and for improvement of bone disease.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedDisease Models, AnimalHumansInterleukin-17Interleukin-6MaleMiceMultiple MyelomaOsteoclastsSyndecan-1Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedIL17A protein, humanInterleukin-17Interleukin-6secukinumabSyndecan-1

Identifiers

PMID26293646
PMCPMC4740263
OpenAlexW2208752319

What OpenQuestion holds

Textmetadata
LicenceTDM
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.