Ion channels in innate and adaptive immunity

S Feske, H Wulff, EY Skolnik - Annual review of immunology, 2015 - annualreviews.org
Ion channels and transporters mediate the transport of charged ions across hydrophobic
lipid membranes. In immune cells, divalent cations such as calcium, magnesium, and zinc …

Clinical, immunological, and genetic features in patients with activated PI3Kδ syndrome (APDS): a systematic review

M Jamee, S Moniri, M Zaki-Dizaji, P Olbrich… - Clinical Reviews in …, 2020 - Springer
Activated phosphoinositide 3-kinase delta syndrome (APDS) is a novel primary
immunodeficiency (PID) caused by heterozygous gain of function mutations in PI3Kδ …

Mg2+ Regulates Cytotoxic Functions of NK and CD8 T Cells in Chronic EBV Infection Through NKG2D

B Chaigne-Delalande, FY Li, GM O'Connor, MJ Lukacs… - Science, 2013 - science.org
The magnesium transporter 1 (MAGT1) is a critical regulator of basal intracellular free
magnesium (Mg2+) concentrations. Individuals with genetic deficiencies in MAGT1 have …

Treatment of E pstein B arr virus‐induced haemophagocytic lymphohistiocytosis with rituximab‐containing chemo‐immunotherapeutic regimens

DB Chellapandian, R Das, K Zelley… - British journal of …, 2013 - Wiley Online Library
Haemophagocytic lymphohistiocytosis (HLH) is a life threatening complication of E pstein–B
arr virus (EBV) infection. The anti‐CD 20 antibody rituximab depletes B cells, leading to …

XMEN disease: a new primary immunodeficiency affecting Mg2+ regulation of immunity against Epstein-Barr virus

FY Li, B Chaigne-Delalande, H Su… - Blood, The Journal …, 2014 - ashpublications.org
Epstein-Barr virus (EBV) is an oncogenic gammaherpesvirus that infects and persists in 95%
of adults worldwide and has the potential to cause fatal disease, especially lymphoma, in …

Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry

A Aghamohammadi, P Mohammadinejad… - Journal of clinical …, 2014 - Springer
Background Primary immunodeficiency disorders (PID) are a group of heterogeneous
disorders mainly characterized by severe and recurrent infections and increased …

Epstein–Barr virus-associated B-cell lymphoproliferative disorders and lymphomas: a review

ML Marques-Piubelli, YI Salas, C Pachas… - Pathology, 2020 - Elsevier
In this review, we focus on B-cell lymphoproliferative disorders (LPDs) and lymphomas
associated with Epstein–Barr virus (EBV). In some of these diseases—such as EBV-positive …

Malignancy in common variable immunodeficiency: a systematic review and meta-analysis

F Kiaee, G Azizi, H Rafiemanesh… - Expert review of …, 2019 - Taylor & Francis
Background: Common variable immunodeficiency (CVID) is the most common clinically
significant primary immunodeficiency (PID) disorder characterized by variable clinical …

[HTML][HTML] Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice

BT Costa-Carvalho, AS Grumach, JL Franco… - Journal of clinical …, 2014 - Springer
Purpose Patients with primary immunodeficiency diseases (PIDD) may present with
recurrent infections affecting different organs, organ-specific inflammation/autoimmunity, and …

[HTML][HTML] A systematic review on predisposition to lymphoid (B and T cell) neoplasias in patients with primary immunodeficiencies and immune dysregulatory disorders …

IB Riaz, W Faridi, MM Patnaik, RS Abraham - Frontiers in immunology, 2019 - frontiersin.org
Primary immunodeficiencies and immune dysregulatory disorders (PIDDs; now referred to
as inborn errors in immunity) are rare disorders with a prevalence of 41. 4 or 50.5 per …