Evidence map›Paper›PMID 21513969›Full record

ReviewThe Journal of allergy and clinical immunology2011

Induction of tolerance to parental parathyroid grafts using allogeneic thymus tissue in patients with DiGeorge anomaly.

Ivan K Chinn, M Louise Markert

Abstract readReview
In one paragraph

Review in The Journal of allergy and clinical immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Informed clinical decisions by outfoxing human FOXN1 variants.The Journal of allergy and clinical immunology · 2025
    Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. 22q11 deletion syndrome: current perspective.The application of clinical genetics · 2015
    Review
  7. Review
  8. Article
  9. Review
  10. Advances in basic and clinical immunology in 2011.The Journal of allergy and clinical immunology · 2012
    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

2 authors at 2 institutions in 1 country.

Ivan K ChinnDepartment of Pediatrics, Division of Allergy and Immunology, Duke University Medical Center, Durham, NC 27710, USA. chinn001@mc.duke.edu
M Louise Markert
Duke Medical Center · USDuke University · US

Funding

THYMIC TRANSPLANTATION IN COMPLETE DIGEORGE SYNDROMER01AI047040 · NIAID · DUKE UNIVERSITY · PI MARKERT, M. LOUISE · 1999 to 2014
$8.0M
RESEARCH TRAINING IN ALLERGY AND CLINICAL IMMUNOLOGYT32AI007062 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David B. Peden, John W. Sleasman · 1985 to 2026
$6.1M
Center for Molecular &Cellular Studies of Ped DiseaseK12HD043494 · NICHD · DUKE UNIVERSITY · PI REED, ANN M. · 2003 to 2017
$5.2M
Parathyroid and Thymus Transplants in DiGeorge SyndromeR21AI060967 · NIAID · DUKE UNIVERSITY · PI MARKERT, MARY LOUISE · 2004 to 2005
$396k
NCRR NIH HHS M03 RR 30NIAID NIH HHS L40 AI079879NIAID NIH HHS R01 AI 047040NIAID NIH HHS R01 AI047040NIAID NIH HHS R21 AI 060967NIAID NIH HHS R21 AI060967NIAID NIH HHS T32 AI007062NIAID NIH HHS T32 AI 007062-28A2NICHD NIH HHS 2 K12 HD043494NICHD NIH HHS K12 HD043494
6 · The paper itself

Abstract

DiGeorge anomaly can affect both thymic and parathyroid function. Although athymia is corrected by allogeneic thymus transplantation, treatment options for hypoparathyroidism have been unsatisfactory. Parathyroid transplantation offers the potential for definitive cure but remains challenging because of graft rejection. Some allogeneic parathyroid grafts have functioned in adult recipients in the context of immunosuppression for renal transplantation. Other efforts have attempted to reduce the allogenicity of the parathyroid grafts through manipulation of the parathyroid tissues before transplantation (by using encapsulation or special culture techniques). Recently, we demonstrated the efficacy of parental parathyroid transplantation when combined with allogeneic thymus transplantation in an infant with complete DiGeorge anomaly. The recipient developed tolerance toward the parathyroid donor. The parathyroid graft has functioned for 5 years after transplantation without the need for continued immunosuppression or calcium supplementation. We observed that matching of the allogeneic thymus graft to the parathyroid donor HLA class II alleles that are unshared with the recipient appears to be associated with the induction of tolerance toward the parathyroid graft. Further work is needed to determine the optimal means for using combined allogeneic thymus and parental parathyroid transplantation to correct hypoparathyroidism in patients with both complete and partial DiGeorge anomaly.

Indexed as

AdultAllelesAnimalsDiGeorge SyndromeFemaleGenes, MHC Class IIHumansImmune ToleranceInfantMaleModels, AnimalModels, ImmunologicalParathyroid GlandsParentsThymus GlandTransplantation, Homologous

Identifiers

PMID21513969
PMCPMC3109298
OpenAlexW1980473689

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.