Evidence map›Paper›PMID 35590415›Full record

ReviewJournal of hematology & oncology2022

Worked to the bone: antibody-based conditioning as the future of transplant biology.

James M Griffin, Fiona M Healy, Lekh N Dahal, Yngvar Floisand, John F Woolley

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.5field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Clinical hematopoietic stem cell-based gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
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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

5 authors at 1 institution in 1 country.

James M GriffinDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Fiona M HealyDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Lekh N DahalDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Yngvar FloisandDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
John F WoolleyDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK. john.woolley@liverpool.ac.uk.
University of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conditioning of the bone marrow prior to haematopoietic stem cell transplant is essential in eradicating the primary cause of disease, facilitating donor cell engraftment and avoiding transplant rejection via immunosuppression. Standard conditioning regimens, typically comprising chemotherapy and/or radiotherapy, have proven successful in bone marrow clearance but are also associated with severe toxicities and high incidence of treatment-related mortality. Antibody-based conditioning is a developing field which, thus far, has largely shown an improved toxicity profile in experimental models and improved transplant outcomes, compared to traditional conditioning. Most antibody-based conditioning therapies involve monoclonal/naked antibodies, such as alemtuzumab for graft-versus-host disease prophylaxis and rituximab for Epstein-Barr virus prophylaxis, which are both in Phase II trials for inclusion in conditioning regimens. Nevertheless, alternative immune-based therapies, including antibody-drug conjugates, radio-labelled antibodies and CAR-T cells, are showing promise in a conditioning setting. Here, we analyse the current status of antibody-based drugs in pre-transplant conditioning regimens and assess their potential in the future of transplant biology.

Indexed as

Epstein-Barr Virus InfectionsGraft vs Host DiseaseHematopoietic Stem Cell TransplantationAntibodies, MonoclonalBiologyHerpesvirus 4, HumanHumansTransplantation ConditioningAntibodies, MonoclonalAntibody–drug conjugateConditioningGraft-versus-host diseaseGraft versus leukaemiaImmunotherapyMonoclonal antibodyStem cell transplant

Identifiers

PMID35590415
PMCPMC9118867
OpenAlexW4280502658

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.