Evidence map›Paper›PMID 30300141›Full record

ArticleThe Journal of clinical investigation2019

Bone marrow transplantation generates T cell-dependent control of myeloma in mice.

Slavica Vuckovic, Simone A Minnie, David Smith, Kate H Gartlan, Thomas S Watkins, Kate A Markey, Pamela Mukhopadhyay, Camille Guillerey, Rachel D Kuns, Kelly R Locke and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. EomesoderminImmunity · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. TIM-3Science immunology · 2024
    Article
  11. Article
  12. Single-cell analysis of the CD8Haematologica · 2024
    Article
  13. Review
  14. Harnessing Dendritic Cells: Next Frontier for Durable Immune Control in Myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 3 countries.

Slavica VuckovicQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Simone A MinnieQIMR Berghofer Medical Research Institute, Brisbane, Australia.
David SmithQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Kate H GartlanQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Thomas S WatkinsQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Kate A MarkeyQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Pamela MukhopadhyayQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Camille GuillereyQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Rachel D KunsQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Kelly R LockeQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Antonia L PritchardQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Peter A JohanssonQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Antiopi VareliasQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Ping ZhangQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Nicholas D HuntingtonMolecular Immunology Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Nicola WaddellQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Marta ChesiComprehensive Cancer Center, Mayo Clinic, Scottsdale, Arizona, USA.
John J MilesCentre for Biodiscovery and Molecular Development of Therapeutics, Australian Institute of Tropical Health and Medicine (AITHM), James Cook University, Cairns, Australia.
Mark J SmythQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Geoffrey R HillQIMR Berghofer Medical Research Institute, Brisbane, Australia.
QIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUAustralian Institute of Tropical Health and Medicine · AUMayo Clinic in Arizona · USMemorial Sloan Kettering Cancer Center · USThe University of Melbourne · AU

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
Project 3 - Modeling Proteasome Inhibitor Response and Resistance in Cell Lines and Patient Samples with Single Cell Analysis of SubpopulationsU54CA224018 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2017 to 2021
$6.0M
Credentialing a Genetically Engineered Clinically-Relevant Mouse Model of Multiple MyelomaR01CA234181 · NCI · MAYO CLINIC ARIZONA · PI CHESI, MARTA · 2019 to 2023
$1.9M
PQD2 Rational Combination of Standard Agents and Immunotherapy to Treat MyelomaR01CA190045 · NCI · MAYO CLINIC ARIZONA · PI CHESI, MARTA · 2014 to 2017
$1.4M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA190045NCI NIH HHS R01 CA234181
6 · The paper itself

Abstract

Transplantation with autologous hematopoietic progenitors remains an important consolidation treatment for patients with multiple myeloma (MM) and is thought to prolong the disease plateau phase by providing intensive cytoreduction. However, transplantation induces inflammation in the context of profound lymphodepletion that may cause hitherto unexpected immunological effects. We developed preclinical models of bone marrow transplantation (BMT) for MM using Vk*MYC myeloma-bearing recipient mice and donor mice that were myeloma naive or myeloma experienced to simulate autologous transplantation. Surprisingly, we demonstrated broad induction of T cell-dependent myeloma control, most efficiently from memory T cells within myeloma-experienced grafts, but also through priming of naive T cells after BMT. CD8+ T cells from mice with controlled myeloma had a distinct T cell receptor (TCR) repertoire and higher clonotype overlap relative to myeloma-free BMT recipients. Furthermore, T cell-dependent myeloma control could be adoptively transferred to secondary recipients and was myeloma cell clone specific. Interestingly, donor-derived IL-17A acted directly on myeloma cells expressing the IL-17 receptor to induce a transcriptional landscape that promoted tumor growth and immune escape. Conversely, donor IFN-γ secretion and signaling were critical to protective immunity and were profoundly augmented by CD137 agonists. These data provide new insights into the mechanisms of action of transplantation in myeloma and provide rational approaches to improving clinical outcomes.

Indexed as

Bone Marrow TransplantationImmunity, CellularImmunologic MemoryAnimalsCD8-Positive T-LymphocytesInterferon-gammaInterleukin-17MiceMice, KnockoutMultiple MyelomaNeoplasm ProteinsNeoplasms, ExperimentalReceptors, Antigen, T-CellReceptors, Interleukin-17Transplantation, HomologousTumor Necrosis Factor Receptor Superfamily, Member 9IFNG protein, mouseIl17a protein, mouseIl17ra protein, mouseInterferon-gammaInterleukin-17Neoplasm ProteinsReceptors, Antigen, T-CellReceptors, Interleukin-17Tumor Necrosis Factor Receptor Superfamily, Member 9ImmunologyImmunotherapyStem cell transplantationT cellsTransplantation

Identifiers

PMID30300141
PMCPMC6307976
OpenAlexW2895911012

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.