Evidence map›Paper›PMID 11435463›Full record

ArticleThe Journal of clinical investigation2001

Familial CD8 deficiency due to a mutation in the CD8 alpha gene.

O de la Calle-Martin, M Hernandez, J Ordi, N Casamitjana, J I Arostegui, I Caragol, M Ferrando, M Labrador, J L Rodriguez-Sanchez, T Espanol

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In one paragraph

Article in The Journal of clinical investigation, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

33 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
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  11. Human inborn errors of immunity to herpes viruses.Current opinion in immunology · 2020
    Review
  12. Review
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  15. Article
  16. Overview of Immunodeficiency Disorders.Immunology and allergy clinics of North America · 2015
    Review
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 2 institutions in 1 country.

O de la Calle-MartinDepartment of Immunology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. odlcalle@hsp.santpau.es
M Hernandez
J Ordi
N Casamitjana
J I Arostegui
I Caragol
M Ferrando
M Labrador
J L Rodriguez-Sanchez
T Espanol
Hospital de Sant Pau · ESVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD8 glycoproteins play an important role in both the maturation and function of MHC class I-restricted T lymphocytes. A 25-year-old man, from a consanguineous family, with recurrent bacterial infections and total absence of CD8(+) cells, was studied. Ab deficiencies and ZAP-70 and TAP defects were ruled out. A missense mutation (gly90-->ser) in both alleles of the immunoglobulin domain of the CD8 alpha gene was shown to correlate with the absence of CD8 expression found in the patient and two sisters. Conversely, high percentages of CD4(-)CD8(-)TCR alpha beta(+) T cells were found in the three siblings. A novel autosomal recessive immunologic defect characterized by absence of CD8(+) cells is described. These findings may help to further understanding of the role of CD8 molecules in human immune response.

Indexed as

Amino Acid SubstitutionMutation, MissenseAdultAnimalsAntibody FormationBacterial InfectionsCD8 AntigensChlorocebus aethiopsConsanguinityCOS CellsCytotoxicity, ImmunologicDimerizationDNA Mutational AnalysisFemaleGenes, RecessiveGenotypeCD8 AntigensProtein SubunitsRecombinant Fusion Proteins

Identifiers

PMID11435463
PMCPMC209336
OpenAlexW1963646172

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.