Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma.
Clin Infect Dis
; 68(11): 1938-1941, 2019 05 17.
Article
in En
| MEDLINE
| ID: mdl-30778533
Biallelic mutations in the ITK gene cause a T-cell primary immunodeficiency with Epstein-Barr virus (EBV)-lymphoproliferative disorders. We describe a novel association of a homozygous ITK mutation with ß-human papillomavirus (HPV)-positive epidermodysplasia verruciformis. Thus, loss of function in ITK can result in broad dysregulation of T-cell responses to oncogenic viruses, including ß-HPV and EBV.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Epidermodysplasia Verruciformis
/
Protein-Tyrosine Kinases
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Hodgkin Disease
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T-Lymphocytes
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Loss of Function Mutation
Type of study:
Prognostic_studies
Limits:
Adult
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Female
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Humans
/
Male
Language:
En
Journal:
Clin Infect Dis
Journal subject:
DOENCAS TRANSMISSIVEIS
Year:
2019
Type:
Article