Evidence map›Paper›PMID 27157594›Full record

ReviewExperimental hematology2016

To condition or not to condition-That is the question: The evolution of nonmyeloablative conditions for transplantation.

Anna Rita Migliaccio

Abstract readHistorical ArticleReview
In one paragraph

Review in Experimental hematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

1 author.

Anna Rita MigliaccioTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY; Department of Biomedical and Neuromotorial Sciences, Alma Mater University, Bologna, Italy. Electronic address: annarita.migliaccio@mssm.edu.

Funding

Tissue BankP01CA108671 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ross L Levine · 2006 to 2026
$82.0M
The human glucocorticoid receptor and normal and pathological terminal erythroidR01HL116329 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MIGLIACCIO, ANNA RITA F · 2012 to 2015
$1.7M
NCI NIH HHS P01 CA108671NHLBI NIH HHS R01 HL116329
6 · The paper itself

Abstract

In 1985, Eugene Cronkite and his colleagues published, in Experimental Hematology, data indicating that five consecutive "transfusions" of large numbers of marrow cells significantly increase the number of donor-derived cells detected by day 10 of a spleen colony-forming assay, the most primitive hematopoietic cells detectable at that time, present in the host for as long as 2 months posttransfusion (Cronkite EP, Bullis JE, Brecher G. Marrow transfusions increase pluripotent stem cells in normal hosts. Exp Hematol 1985;13:802-805). These data provided the first evidence that donor hematopoietic stem cells (HSCs) may persist in vivo for some time in recipients when transfused and not transplanted, that is, not subjected to treatments that deplete their marrow niches of endogenous HSCs. The limited technology available at the time prevented Dr. Cronkite from pursuing this observation into the development of nonmyeloablated transplantation procedures, and his experiment, as well as the term bone marrow transfusion, has since been long forgotten. In recent years, the scientific need to clarify HSC functions in nonstressed hosts and the clinical need to develop transplantation procedures with levels of morbidity/mortality acceptable for curing inherited hematologic disorders have inspired the search for nonmyeloablative transplantation procedures, including methods that "outcompete" endogenous host HSCs such as those pioneered by Dr. Cronkite's experiments using high transfusion doses. This review describes the technical progress made since Dr. Cronkite's insightful work, which has finally found its path to the clinic.

Indexed as

Bone Marrow TransplantationHematopoietic Stem Cell TransplantationTransplantation ConditioningAnimalsGraft RejectionGraft SurvivalGraft vs Host DiseaseHematopoietic Stem CellsHemoglobinopathiesHistory, 20th CenturyHumansMiceModels, AnimalTransplantation Chimera

Identifiers

PMID27157594
PMCPMC5778909

What Socratic 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 Socratic graph.