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Combined immunodeficiency with EBV positive B cell lymphoma and epidermodysplasia verruciformis due to a novel homozygous mutation in RASGRP1.

Authors :
Platt, Craig D.
Fried, Ari J.
Hoyos-Bachiloglu, Rodrigo
Chou, Janet
Geha, Raif S.
Usmani, G. Naheed
Schmidt, Birgitta
Chiarle, Roberto
Whangbo, Jennifer
Source :
Clinical Immunology. Oct2017, Vol. 183, p142-144. 3p.
Publication Year :
2017

Abstract

RASGRP1 is a guanine-nucleotide-exchange factor essential for MAP-kinase mediated signaling in lymphocytes. We report the second case of RASGRP1 deficiency in a patient with a homozygous nonsense mutation in the catalytic domain of the protein. The patient had epidermodysplasia verruciformis, suggesting a clinically important intrinsic T cell function defect. Like the previously described patient, our proband also presented with CD4 + T cell lymphopenia, impaired T cell proliferation to mitogens and antigens, reduced NK cell function, and EBV-associated lymphoma. The severity of the disease and the development of EBV lymphoma in both patients suggest that hematopoietic stem cell transplantation should be performed rapidly in patients with RASGRP1 deficiency. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15216616
Volume :
183
Database :
Academic Search Index
Journal :
Clinical Immunology
Publication Type :
Academic Journal
Accession number :
125983147
Full Text :
https://doi.org/10.1016/j.clim.2017.08.007