Evidence map›Paper›PMID 25075835›Full record

ArticleThe New England journal of medicine2014

Transplantation outcomes for severe combined immunodeficiency, 2000-2009.

Sung-Yun Pai, Brent R Logan, Linda M Griffith, Rebecca H Buckley, Roberta E Parrott, Christopher C Dvorak, Neena Kapoor, Imelda C Hanson, Alexandra H Filipovich, Soma Jyonouchi and 29 more

6 registry-linked trialsOpen access · bronzeAbstract readMulticenter Study
In one paragraph

Article in The New England journal of medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 6 registered trials, which are not on this map. Cited by 350 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
350citing papers in PubMed, 3 pooled it
27.2field-weighted citation impact, top 1% 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.

NCT01186913 enrolling by invitationnot on this map

A Prospective Natural History Study of Diagnosis, Treatment and Outcomes of Children With SCID Disorders (RDCRN PIDTC-6901)

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2010 to 2028Enrolled690ConditionsSevere Combined Immunodeficiency (SCID), Leaky SCID, Omenn Syndrome, Reticular Dysgenesis
NCT01346150 unknown statusnot on this map

A Retrospective and Cross-Sectional Analysis of Patients Treated for SCID Since January 1,1968 (RDCRN PIDTC-6902)

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2011 to 2023Enrolled1,007ConditionsSCID, ADA-SCID, XSCID, Leaky SCID
NCT02064933 completednot on this map

Analysis of Patients Treated for Wiskott-Aldrich Syndrome Since January 1, 1990 (RDCRN PIDTC-6904)

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2014 to 2019Enrolled305ConditionsWiskott-Aldrich Syndrome
NCT02082353 unknown statusnot on this map

Analysis of Patients Treated for Chronic Granulomatous Disease Since January 1, 1995

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2014 to 2021Enrolled1,480ConditionsGranulomatous Disease, Chronic
NCT03538899 phase1 / phase2recruitingnot on this mapstarted 2018, after this paper: background citation

Phase I/II Safety and Efficacy Study of Gene Transfer for Artemis-Deficient Severe Combined Immunodeficiency (ART-SCID) in Newly Diagnosed Patients Using Self-Inactivating Lentiviral Vector (AProArt) to Transduce Autologous CD34 Hematopoietic Cells

TypeinterventionalSponsorUniversity of California, San FranciscoRan2018 to 2038Enrolled24ConditionsSevere Combined ImmunodeficiencyArmsAProArt-CD34, CliniMACS® CD34 Reagent System cell sorter device, Busulfan
NCT04172181 unknown statusnot on this mapstarted 2019, after this paper: background citation

Multi-center Clinical Study of Cord Blood Stem Cell Transplantation for Severe Combined Immunodeficiency Disease

TypeobservationalSponsorChildren's Hospital of Fudan UniversityRan2019 to 2023Enrolled50ConditionsSevere Combined Immunodeficiency DiseaseArmscord blood stem cell transplantation
3 · Its place in the literature

Who cites it

350 citing papers in PubMed, 3 syntheses or guidelines pooled it, 759 citations in OpenAlex.

  1. Pooled it
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  16. Restoration of the immune system with base editing and non-genotoxic conditioning in a Rag2 point-mutant mouse model.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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290 more citing papers are in PubMed but not listed here.

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

39 authors at 20 institutions in 2 countries.

Sung-Yun PaiThe authors' affiliations are listed in the Appendix.
Brent R Logan
Linda M Griffith
Rebecca H Buckley
Roberta E Parrott
Christopher C Dvorak
Neena Kapoor
Imelda C Hanson
Alexandra H Filipovich
Soma Jyonouchi
Kathleen E Sullivan
Trudy N Small
Lauri Burroughs
Suzanne Skoda-Smith
Ann E Haight
Audrey Grizzle
Michael A Pulsipher
Ka Wah Chan
Ramsay L Fuleihan
Elie Haddad
Brett Loechelt
Victor M Aquino
Alfred Gillio
Jeffrey Davis
Alan Knutsen
Angela R Smith
Theodore B Moore
Marlis L Schroeder
Frederick D Goldman
James A Connelly
Matthew H Porteus
Qun Xiang
William T Shearer
Thomas A Fleisher
Donald B Kohn
Jennifer M Puck
Luigi D Notarangelo
Morton J Cowan
Richard J O'Reilly
Memorial Sloan Kettering Cancer Center · USBaylor College of Medicine · USNational Institutes of Health · USUniversity of California, Los Angeles · USAflac (United States) · USBoston Children's Hospital · USCancer Research Center · USCardinal Glennon Children’s Medical Center · USChildren's Healthcare of Atlanta · USChildren's Hospital of Philadelphia · USChildren's National · USFred Hutch Cancer Center · USHarvard Stem Cell Institute · USHuntsman Cancer Institute · USLurie Children's Hospital · USMethodist Children’s Hospital · USStanford University · USThe University of Texas Southwestern Medical Center · USUCSF Benioff Children's Hospital · USUniversité de Montréal · CA

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
T LYMPHOCYTE SUBSET FUNCTION POST-TRANSPLANTATIONP01CA023766 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PAMER, ERIC G. · 1985 to 2023
$59.0M
UNRELATED AND HLA-MISMATCHED RELATED DONOR TRANSPLANTSP01HL036444 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RAWLINGS, DAVID J · 1986 to 2010
$25.9M
Training of Clinical Investigators in Primary Immune DeficienciesU54AI082973 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PUCK, JENNIFER M. · 2009 to 2023
$23.3M
Newborn Screening for T-Cell Disorders: Spectrum and OutcomesR01AI105776 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BRENNER, STEVEN E, CHURCH, JOSEPH · 2013 to 2016
$2.4M
Pediatric Blood and Marrow Transplant ConsortiumU01HL069254 · NHLBI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI PULSIPHER, MICHAEL A · 2001 to 2010
$2.0M
Nonmyeloablative Allografting for Immunodeficiency & Other Nonmalignant DisordersK23HL085288 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BURROUGHS, LAURI M. · 2007 to 2010
$546k
Primary Immune Deficiency Treatment Consortium Annual Scientific MeetingR13AI094943 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PUCK, JENNIFER M. · 2011 to 2025
$239k
NCI NIH HHS CA23766NCI NIH HHS P01 CA023766NCI NIH HHS P30 CA014236NHLBI NIH HHS 2U01HL069254NHLBI NIH HHS HL085288NHLBI NIH HHS HL36444NHLBI NIH HHS K23 HL085288NHLBI NIH HHS P01 HL036444NHLBI NIH HHS U01 HL069254NIAID NIH HHS 1U54AI082973NIAID NIH HHS R01 AI105776NIAID NIH HHS R13 AI094943NIAID NIH HHS R13AI094943NIAID NIH HHS U54 AI082973
6 · The paper itself

Abstract

backgroundThe Primary Immune Deficiency Treatment Consortium was formed to analyze the results of hematopoietic-cell transplantation in children with severe combined immunodeficiency (SCID) and other primary immunodeficiencies. Factors associated with a good transplantation outcome need to be identified in order to design safer and more effective curative therapy, particularly for children with SCID diagnosed at birth.

methodsWe collected data retrospectively from 240 infants with SCID who had received transplants at 25 centers during a 10-year period (2000 through 2009).

resultsSurvival at 5 years, freedom from immunoglobulin substitution, and CD3+ T-cell and IgA recovery were more likely among recipients of grafts from matched sibling donors than among recipients of grafts from alternative donors. However, the survival rate was high regardless of donor type among infants who received transplants at 3.5 months of age or younger (94%) and among older infants without prior infection (90%) or with infection that had resolved (82%). Among actively infected infants without a matched sibling donor, survival was best among recipients of haploidentical T-cell-depleted transplants in the absence of any pretransplantation conditioning. Among survivors, reduced-intensity or myeloablative pretransplantation conditioning was associated with an increased likelihood of a CD3+ T-cell count of more than 1000 per cubic millimeter, freedom from immunoglobulin substitution, and IgA recovery but did not significantly affect CD4+ T-cell recovery or recovery of phytohemagglutinin-induced T-cell proliferation. The genetic subtype of SCID affected the quality of CD3+ T-cell recovery but not survival.

conclusionsTransplants from donors other than matched siblings were associated with excellent survival among infants with SCID identified before the onset of infection. All available graft sources are expected to lead to excellent survival among asymptomatic infants. (Funded by the National Institute of Allergy and Infectious Diseases and others.).

Indexed as

Hematopoietic Stem Cell TransplantationCD3 ComplexFemaleGraft vs Host DiseaseHumansImmunoglobulin AIncidenceInfantLymphocyte CountMaleRetreatmentRetrospective StudiesSevere Combined ImmunodeficiencySiblingsSurvival RateT-LymphocytesCD3 ComplexImmunoglobulin A

Identifiers

PMID25075835
PMCPMC4183064
OpenAlexW2122153475

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Registered trials

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.