Evidence map›Paper›PMID 20109609›Full record

ReviewSeminars in hematology2010

Unrelated umbilical cord blood transplantation and immune reconstitution.

Paul Szabolcs, Mitchell S Cairo

Abstract readReview
In one paragraph

Review in Seminars in hematology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Loss of T Follicular Helper Cells in the Peripheral Blood of Patients with Chronic Graft-versus-Host Disease.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2016
    Article
  13. Infectious Complications after Umbilical Cord-Blood Transplantation from Unrelated Donors.Mediterranean journal of hematology and infectious diseases · 2016
    Review
  14. Review
  15. Development of a diverse human T-cell repertoire despite stringent restriction of hematopoietic clonality in the thymus.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  16. Primary Immune Deficiency Treatment Consortium (PIDTC) report.The Journal of allergy and clinical immunology · 2014
    Article
  17. Review
  18. Article
  19. Article
  20. Immune recovery in adult patients after myeloablative dual umbilical cord blood, matched sibling, and matched unrelated donor hematopoietic cell transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2012
    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

2 authors.

Paul SzabolcsDepartment of Pediatrics, Division of Pediatric Bone Marrow Transplantation, Duke University Medical Center, Durham, NC, USA.
Mitchell S Cairo

Funding

Preclinical studies of unrelated cord blood transplantationP01HL067314 · NHLBI · DUKE UNIVERSITY · PI CHAO, NELSON J. · 2002 to 2005
$6.9M
Graft Engineering and Immunotherapy After Unrelated Cord Blood TransplantationR01CA132110 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SZABOLCS, PAUL · 2007 to 2011
$1.5M
Nonablative AlloSCT in Refractory Autoimmune DiseaseR21AR049330 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CAIRO, MITCHELL S. · 2002 to 2003
$164k
TRANSPLANT CENTER FOR UMBILICAL CORD STEM CELLN01HB067136 · HB · CHILDREN'S HOSPITAL OF ORANGE COUNTY · PI CAIRO, MITCHELL S. · 1996 to 1998
–
NCI NIH HHS R01 CA132110NCI NIH HHS R01-CA132110NHLBI NIH HHS 1P01-HL-67314-01A1NHLBI NIH HHS N01-HB-67136NHLBI NIH HHS P01 HL067314NIAMS NIH HHS R21 AR049330NIAMS NIH HHS R21 AR49330
6 · The paper itself

Abstract

This review highlights the unique features of immune reconstitution following unrelated cord blood transplantation (UCBT) that lead to heightened risk of infection-related mortality in the early post-UCBT period. There is no evidence that innate immunity is uniquely compromised after UCBT, but the development of antigen-specific cellular immunity is affected by numerical and qualitative deficits, primarily within the first 100 days. Nevertheless, beyond the first few months after UCBT there is no evidence for reduced graft-versus-leukemia (GVL) or anti-viral immunity compared to other hematopoietic cell therapy (HCT) modalities. Novel cellular therapies that are about to enter the clinical setting in the form of natural killer (NK) cell and T-cell therapies in the form of donor lymphocyte infusion (DLI) are also discussed.

Indexed as

Cord Blood Stem Cell TransplantationHematopoietic Stem Cell TransplantationImmunosuppression TherapyAdultBlood DonorsChildCommunicable DiseasesHematologic DiseasesHematologic NeoplasmsHumansKiller Cells, NaturalLymphocyte SubsetsMyeloablative AgonistsPatient SelectionRecurrenceRisk AssessmentMyeloablative Agonists

Identifiers

PMID20109609
PMCPMC3684393

What OpenQuestion holds

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Registered trials

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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.