Evidence map›Paper›PMID 31085833›Full record

ArticleThe Journal of clinical investigation2019

Targeting VLA4 integrin and CXCR2 mobilizes serially repopulating hematopoietic stem cells.

Darja Karpova, Michael P Rettig, Julie Ritchey, Daniel Cancilla, Stephanie Christ, Leah Gehrs, Ezhilarasi Chendamarai, Moses O Evbuomwan, Matthew Holt, Jingzhu Zhang and 17 more

Open access · hybridAbstract 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 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Extramedullary hematopoiesis in cancer.Experimental & molecular medicine · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Purinergic Signaling and Its Role in Mobilization of Bone Marrow Stem Cells.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  19. Article
  20. Experimental and therapeutic medicine · 2022
    Article
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

27 authors at 6 institutions in 2 countries.

Darja KarpovaDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Michael P RettigDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Julie RitcheyDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Daniel CancillaDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Stephanie ChristDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Leah GehrsDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Ezhilarasi ChendamaraiDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Moses O EvbuomwanOakland University William Beaumont School of Medicine, Rochester, Michigan, USA.
Matthew HoltDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Jingzhu ZhangDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Grazia Abou-EzziDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Hamza CelikDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Eliza WiercinskaGerman Red Cross Blood Service and Institute for Transfusion Medicine and Immunohematology of the Goethe University, Frankfurt, Germany.
Wei YangGenome Technology Access Center, Washington University, St. Louis, Missouri, USA.
Feng GaoDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Linda G EissenbergDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Richard F HeierCenter for World Health and Medicine, Saint Louis University, St. Louis, Missouri, USA.
Stacy D ArnettCenter for World Health and Medicine, Saint Louis University, St. Louis, Missouri, USA.
Marvin J MeyersCenter for World Health and Medicine, Saint Louis University, St. Louis, Missouri, USA.
Michael J PrinsenCenter for World Health and Medicine, Saint Louis University, St. Louis, Missouri, USA.
David W GriggsCenter for World Health and Medicine, Saint Louis University, St. Louis, Missouri, USA.
Andreas TrumppDivision of Stem Cells and Cancer, German Cancer Research Center (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany.
Peter G RuminskiDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Dwight M MorrowMagenta Therapeutics, Cambridge, Massachusetts, USA.
Halvard B BonigGerman Red Cross Blood Service and Institute for Transfusion Medicine and Immunohematology of the Goethe University, Frankfurt, Germany.
Daniel C LinkDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
John F DiPersioDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Washington University in St. Louis · USSaint Louis University · USGerman Cancer Research Center · DEGoethe University Frankfurt · DEFate Therapeutics (United States) · USOakland University · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Specimen Acquistition and Expression ProfilingP01CA101937 · NCI · WASHINGTON UNIVERSITY · PI LINK, DANIEL C · 2003 to 2023
$58.8M
Washington University Institute of Clinical and Translational Sciences (UL1)UL1RR024992 · NCRR · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2007 to 2011
$45.4M
Targeting the Bone Marrow Microenvironment In Acute Lymphocytic LeukemiaP50CA171963 · NCI · WASHINGTON UNIVERSITY · PI Daniel C Link · 2013 to 2026
$31.6M
Project 2 - Radiation-Induced Treatment of Multiple Myeloma using NanoparticlesU54CA199092 · NCI · WASHINGTON UNIVERSITY · PI ACHILEFU, SAMUEL · 2015 to 2019
$11.5M
Optimizing Hematopoietic Stem Cell Transplantation For The Treatment Of Hematological MalignanciesR35CA210084 · NCI · WASHINGTON UNIVERSITY · PI John F. Dipersio · 2017 to 2026
$7.8M
TARGETING AML-STROMAL INTERACTIONSR01CA152329 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F. · 2011 to 2015
$2.5M
BM NICHE DISRUPTION AND IMMUNOTHERAPY IN HEMATOLOGICAL MALIGNANCIESR50CA211466 · NCI · WASHINGTON UNIVERSITY · PI Michael Rettig · 2016 to 2026
$2.3M
REGULATION OF HEMATOPOIETIC NICHES BY TGF FAMILY SIGNALINGR01HL131655 · NHLBI · WASHINGTON UNIVERSITY · PI LINK, DANIEL C · 2016 to 2019
$1.5M
NCATS NIH HHS UL1 TR002345NCI NIH HHS P01 CA101937NCI NIH HHS P30 CA091842NCI NIH HHS P50 CA171963NCI NIH HHS R01 CA152329NCI NIH HHS R35 CA210084NCI NIH HHS R50 CA211466NCI NIH HHS U54 CA199092NCRR NIH HHS UL1 RR024992NHLBI NIH HHS R01 HL131655
6 · The paper itself

Abstract

Mobilized peripheral blood has become the primary source of hematopoietic stem and progenitor cells (HSPCs) for stem cell transplantation, with a five-day course of granulocyte colony stimulating factor (G-CSF) as the most common regimen used for HSPC mobilization. The CXCR4 inhibitor, plerixafor, is a more rapid mobilizer, yet not potent enough when used as a single agent, thus emphasizing the need for faster acting agents with more predictable mobilization responses and fewer side effects. We sought to improve hematopoietic stem cell transplantation by developing a new mobilization strategy in mice through combined targeting of the chemokine receptor CXCR2 and the very late antigen 4 (VLA4) integrin. Rapid and synergistic mobilization of HSPCs along with an enhanced recruitment of true HSCs was achieved when a CXCR2 agonist was co-administered in conjunction with a VLA4 inhibitor. Mechanistic studies revealed involvement of CXCR2 expressed on BM stroma in addition to stimulation of the receptor on granulocytes in the regulation of HSPC localization and egress. Given the rapid kinetics and potency of HSPC mobilization provided by the VLA4 inhibitor and CXCR2 agonist combination in mice compared to currently approved HSPC mobilization methods, it represents an exciting potential strategy for clinical development in the future.

Indexed as

Hematopoietic Stem Cell MobilizationHematopoietic Stem Cell TransplantationIntegrin alpha4beta1Receptors, Interleukin-8BAllograftsAnimalsBone MarrowGranulocytesHematopoietic Stem CellsMiceMice, Inbred BALB CMice, KnockoutIntegrin alpha4beta1Receptors, Interleukin-8BBone marrow transplantationHematopoietic stem cellsStem cellsTransplantation

Identifiers

PMID31085833
PMCPMC6597242
OpenAlexW2945568759

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.