Evidence map›Paper›PMID 27042837›Full record

ArticleBone marrow transplantation2016

Multi-color immune-phenotyping of CD34 subsets reveals unexpected differences between various stem cell sources.

J Dmytrus, S Matthes-Martin, H Pichler, N Worel, R Geyeregger, N Frank, C Frech, G Fritsch

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Flow Cytometric Characterization of Hematopoietic Stem and Progenitor Cell Subpopulations in Autologous Peripheral Blood Stem Cell Preparations after Cryopreservation.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2023
    Article
  9. Article
  10. Article
  11. Bone Marrow Grafts From Pediatric Donors May Contain A Considerable Number of Hematogones.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Purification of Human CD34Molecular therapy. Methods & clinical development · 2020
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

J DmytrusChildren's Cancer Research Institute, Vienna, Austria.
S Matthes-MartinSt. Anna Children's Hospital, Department of Pediatrics, Medical University, Vienna, Austria.
H PichlerSt. Anna Children's Hospital, Department of Pediatrics, Medical University, Vienna, Austria.
N WorelDepartment for Blood Group Serology and Transfusion Medicine, Medical University, Vienna, Austria.
R GeyereggerChildren's Cancer Research Institute, Vienna, Austria.
N FrankChildren's Cancer Research Institute, Vienna, Austria.
C FrechChildren's Cancer Research Institute, Vienna, Austria.
G FritschChildren's Cancer Research Institute, Vienna, Austria.
St Anna Children's Hospital · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flow cytometric routine CD34 analysis enumerates hematopoietic stem and progenitor cells irrespective of their subpopulations although this might predict engraftment dynamics and immune reconstitution. We established a multi-color CD34 assay containing CD133, CD45RA, CD10, CD38 and CD33. We examined PBSC, donor bone marrow (BMd) and BM of patients 1 year after allografting (BM1y) regarding their CD34 subset composition, which differed significantly amongst those materials: the early CD45RA(-)CD133(+)CD38(low) subpopulations were significantly more frequent in PBSC than in BMd, and very low in BM1y. Vice versa, clearly more committed CD34 stages prevailed in BM, particularly in BM1y where the proportion of multi-lymphoid and CD38(++) B-lymphoid precursors was highest (mean 59%). CD33 was expressed at different intensity on CD45RA(±)CD133(±) subsets allowing discrimination of earlier from more committed myeloid precursors. Compared with conventional CD34(+) cell enumeration, the presented multi-color phenotyping is a qualitative approach defining different CD34 subtypes in any CD34 source. Its potential impact to predict engraftment kinetics and immune reconstitution has to be evaluated in future studies.

Indexed as

ImmunophenotypingAdolescentAdultAgedAllograftsAntigens, CDAntigens, CD34Bone Marrow CellsChildChild, PreschoolFemaleFlow CytometryHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansInfantAntigens, CDAntigens, CD34

Identifiers

PMID27042837
OpenAlexW2335809174

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.