| Literature DB >> 28822832 |
Craig D Platt1, Ari J Fried1, Rodrigo Hoyos-Bachiloglu1, G Naheed Usmani2, Birgitta Schmidt3, Jennifer Whangbo4, Roberto Chiarle3, Janet Chou1, Raif S Geha5.
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.Entities:
Keywords: Epidermodysplasia verruciformis; Epstein Barr Virus; Lymphoma; RASGRP1 deficiency
Mesh:
Substances:
Year: 2017 PMID: 28822832 PMCID: PMC5673555 DOI: 10.1016/j.clim.2017.08.007
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969