Evidence map›Paper›PMID 22116933›Full record

Trial reportScience translational medicine2011

Bactericidal/permeability-increasing protein (rBPI21) and fluoroquinolone mitigate radiation-induced bone marrow aplasia and death.

Eva C Guinan, Christine M Barbon, Leslie A Kalish, Kalindi Parmar, Jeff Kutok, Christy J Mancuso, Liat Stoler-Barak, Eugénie E Suter, Janice D Russell, Christine D Palmer and 9 more

Abstract readClinical Trial
In one paragraph

Trial report in Science translational medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. rBPIAmerican journal of hematology · 2018
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. NRF2 mitigates radiation-induced hematopoietic death.The Journal of clinical investigation · 2014
    Article
  18. Article
  19. Review
  20. Role of innate immunity in neonatal infection.American journal of perinatology · 2013
    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

19 authors at 4 institutions in 1 country.

Eva C GuinanDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Christine M Barbon
Leslie A Kalish
Kalindi Parmar
Jeff Kutok
Christy J Mancuso
Liat Stoler-Barak
Eugénie E Suter
Janice D Russell
Christine D Palmer
Leighanne C Gallington
Annie Voskertchian
Jo-Anne Vergilio
Geoffrey Cole
Kaya Zhu
Alan D'Andrea
Robert Soiffer
Jerrold P Weiss
Ofer Levy
Boston Children's Hospital · USDana-Farber Cancer Institute · USHarvard University · USBrigham and Women's Hospital · US

Funding

Genetic screens for IR resistanceU19AI067751 · NIAID · DANA-FARBER CANCER INSTITUTE · PI D'ANDREA, ALAN D. · 2005 to 2009
$9.9M
rBPI21 & Endotoxin-directed Innate Immunity in Stem Cell TransplantationR21HL089659 · NHLBI · DANA-FARBER CANCER INST · PI GUINAN, EVA C · 2008 to 2009
$489k
NHLBI NIH HHS 5R21 HL089659NHLBI NIH HHS R21 HL089659NIAID NIH HHS 5U19 AI067751NIAID NIH HHS U19 AI067751
6 · The paper itself

Abstract

Identification of safe, effective treatments to mitigate toxicity after extensive radiation exposure has proven challenging. Only a limited number of candidate approaches have emerged, and the U.S. Food and Drug Administration has yet to approve any agent for a mass-casualty radiation disaster. Because patients undergoing hematopoietic stem cell transplantation undergo radiation treatment that produces toxicities similar to radiation-disaster exposure, we studied patients early after such treatment to identify new approaches to this problem. Patients rapidly developed endotoxemia and reduced plasma bactericidal/permeability-increasing protein (BPI), a potent endotoxin-neutralizing protein, in association with neutropenia. We hypothesized that a treatment supplying similar endotoxin-neutralizing activity might replace the BPI deficit and mitigate radiation toxicity and tested this idea in mice. A single 7-Gy radiation dose, which killed 95% of the mice by 30 days, was followed 24 hours later by twice-daily, subcutaneous injections of the recombinant BPI fragment rBPI21 or vehicle alone for 14 or 30 days, with or without an oral fluoroquinolone antibiotic with broad-spectrum antibacterial activity, including that against endotoxin-bearing Gram-negative bacteria. Compared to either fluoroquinolone alone or vehicle plus fluoroquinolone, the combined rBPI21 plus fluoroquinolone treatment improved survival, accelerated hematopoietic recovery, and promoted expansion of stem and progenitor cells. The observed efficacy of rBPI21 plus fluoroquinolone initiated 24 hours after lethal irradiation, combined with their established favorable bioactivity and safety profiles in critically ill humans, suggests the potential clinical use of this radiation mitigation strategy and supports its further evaluation.

Indexed as

Ablation TechniquesAnimalsAntimicrobial Cationic PeptidesBlood Cell CountBlood ProteinsBone MarrowCytokinesEndotoxemiaEndotoxinsEnrofloxacinFluoroquinolonesHematopoiesisHematopoietic Stem Cell TransplantationHumansInflammation MediatorsIntestinal MucosaAntimicrobial Cationic Peptidesbactericidal permeability increasing proteinBlood ProteinsCytokinesEndotoxinsEnrofloxacinFluoroquinolonesInflammation Mediators

Identifiers

PMID22116933
PMCPMC4096810
OpenAlexW2149612654

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.