Evidence map›Paper›PMID 19931163›Full record

ArticlePediatric neurology2009

CD40 ligand deficiency: neurologic sequelae with radiographic correlation.

Shrinivas Bishu, Deepak Madhavan, Phillip Perez, Lucy Civitello, Shuying Liu, Margaret Fessler, Steven M Holland, Ashish Jain, Maryland Pao

Open access · greenAbstract readCase Reports
In one paragraph

Article in Pediatric neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Hyperimmunoglobulin syndromes: A review of HIGM, HIES, and HIDS.Journal of translational autoimmunity · 2025
    Review
  2. Review
  3. Article
  4. Review
  5. Childhood choreoathetosis secondary to hyper-IgM syndrome (CD40 ligand deficiency).Neurology(R) neuroimmunology & neuroinflammation · 2020
    Article
  6. Article
  7. Article
  8. 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

9 authors at 6 institutions in 1 country.

Shrinivas BishuSection on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, National Institutes of Health, 9000 Rockville Pike, Building 10, Room 2D54, Bethesda, MD 20892-1298, USA. shrinivas@uky.edu
Deepak Madhavan
Phillip Perez
Lucy Civitello
Shuying Liu
Margaret Fessler
Steven M Holland
Ashish Jain
Maryland Pao
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USChildren's National · USGeorgetown University · USNational Institute of Mental Health · USUniversity of Nebraska Medical Center · US

Funding

Transgenic Animal Models Of Human Immune DefectsZIAAI000646 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HOLLAND, STEVEN · 2009 to 2025
$22.2M
Psychiatry Consultation Liaison Service ResearchZIAMH002922 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PAO, MARYLAND · 2009 to 2025
$11.5M
Studies of Hyper- IgM SyndromeZIAAI001078 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI JAIN, ASHISH · 2009 to 2011
$1.2M
Intramural NIH HHS NIH0012783015PHS HHS NIH0012783015
6 · The paper itself

Abstract

Patients with CD40 ligand deficiency are susceptible to central nervous system infections, but to date the neurologic progression or long-term outcome of central nervous system complications have not been reported in detail. Characterizing the central nervous system complications of immune deficiencies can lead to the identification of new pathogens. For this study, clinical data were reviewed on patients with both CD40 ligand deficiency and neurodegeneration, identified from a larger cohort of 31 patients. Five patients had progressive neurologic and cognitive decline in the absence of clinical signs of acute fulminant encephalitis, with anatomic brain abnormalities and high mortality (60%). Despite multiple evaluations, no pathogens were identified in four patients, all of whom were on standard intravenous immunoglobulin therapy at illness presentation. This clinical phenotype of progressive decline without acute fulminant encephalitis is similar to chronic enteroviral encephalitis in X-linked agammaglobulinemia, another condition with severe humoral immune defects. Whether infection secondary to subtherapeutic levels of central nervous system immunoglobulin G (IgG), inadequately protective levels of serum IgG, or impaired CD40 ligand-dependent IgG-independent antiviral responses contributed remains undetermined. Emerging gene-chip techniques applied in patients with primary immune deficiencies may identify heretofore unknown viruses. Prospective neurocognitive and evaluation of patients with CD40 ligand deficiency may identify affected patients before overt clinical signs appear.

Indexed as

BrainCD40 LigandChild, PreschoolCognition DisordersDisease ProgressionFollow-Up StudiesHumansHyper-IgM Immunodeficiency Syndrome, Type 1Immunoglobulins, IntravenousImmunologic FactorsInfantMagnetic Resonance ImagingMaleNeurodegenerative DiseasesCD40 LigandImmunoglobulins, IntravenousImmunologic Factors

Identifiers

PMID19931163
PMCPMC3130593
OpenAlexW2017275115

What OpenQuestion holds

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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.