XMEN disease

This image displays select clinical and laboratory manifestations of XMEN disease [3]

XMEN patients have splenomegaly, chronic Epstein Barr Virus (EBV) infection, and are developmentally normal. They have an increased susceptibility for developing EBV+ lymphoma. Additionally, XMEN patients have excessive infections consistent with the underlying immunodeficiency. These infections included recurrent otitis media, sinusitis, viral pneumonia, diarrhea, upper respiratory infections, epiglottitis, and pertussis. Although autoimmune symptoms do not feature prominently in XMEN autoimmune cytopenias were observed in two unrelated patients.[1]

In the figure to the left, major features are present in all XMEN patients, while minor features are found only in some.

XMEN disease is caused by loss of function mutations in the gene MAGT1.[1] MAGT1 is a 70 kb gene with 10 exons encoding for a 335 amino acid protein that maps to Xq21.1.[4] MagT1 is a component of the N-linked glycosylation machinery (oligosacchyrltransferase, OST), a fundamental component of all cells that regulates the attachment of sugar moieties onto specific sites in proteins. Many of the immunodeficiency-related features of XMEN disease are related to the hypoglycosylation phenotype caused by loss of the OST component MagT1.[5][6]

The conclusive connection between MAGT1, glycosylation, and Mg2+ import remains unknown.  A prominent hypothesis from XMEN patients suggests that MAGT1's role in glycosylation is essential to the function (either directly or indirectly) of a Mg+2 transporter.[5][6]

MAGT1 is evolutionarily conserved and expressed in all mammalian cells with higher expression in hematopoietic lineages.[7] XMEN patients have been found to carry both MAGT1 deletions and missense mutations. However, the severity of the phenotype is not entirely explained by the genotype. The disease severity also likely depends on environmental and other genetic factors.[3]

XMEN disease follows an X-linked inheritance pattern because the MAGT1 is located on the X chromosome. Mothers of XMEN patients exhibit preferential X chromosome inactivation of the chromosome with the mutation in their hematopoietic cells and are asymptomatic.

XMEN patients generally have chronically high levels of EBV with increased EBV-infected cells, diminished thymic output of CD4+ cells, reduced CD4:CD8 ratio, moderately high B cell counts, and mild neutropenia. Their neutropenia may be related to their chronic EBV. Some patients also showed defective T cell proliferation in response to mitogen stimulation, variable immunoglobulin deficiencies, or deficient vaccination response.[1][2][3]

Once a diagnosis is made, each individual's treatment is based on an individual’s clinical condition. Hematopoietic stem cell transplant is a possible treatment of this condition but its effectiveness is unproven.

Additionally, magnesium supplementation is a promising potential treatment for XMEN. One of the consequences of loss of MAGT1 function is a decreased level of unbound intracellular Mg2+. This decrease leads to loss of expression of an immune cell receptor called NKG2D, which is involved in EBV-immunity. Remarkably, Mg2+ supplementation can restore NKG2D expression and other functions that are abnormal in patients with XMEN disease. Early evidence suggests continuous oral magnesium threonate supplementation is safe and well tolerated. Nonetheless, further research is needed to evaluate the use of Mg2+ as a treatment for XMEN. It remains unclear if such supplementation will protect against the development of lymphoma in XMEN patients.[3] Investigators at the National Institute of Allergy and Infectious Diseases at the US National Institutes of Health currently have clinical protocols to study new approaches to the diagnosis and treatment of this disorder.[8][9]