RecruitingNCT06278337

X-linked Moesin Associated Immunodeficiency

Etude Multicentrique Internationale rétrospective Des Patients Atteints de déficit Immunitaire associé à la moésine lié au Chromosome X (X Maid Pour X-linked Moesin Associated Immunodeficiency)


Sponsor

Institut National de la Santé Et de la Recherche Médicale, France

Enrollment

16 participants

Start Date

Aug 12, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

Moesin deficiency was initially described in 7 male participants aged 4 to 69 years and is characterized by lymphopenia of the 3 lineages and moderate neutropenia. Genetically, 6 out of 7 participants had the same missense mutation in the moesin gene located on the X chromosome. The 7th patient has a mutation leading to the premature introduction of a STOP codon into the protein.Clinically the 7 participants with X-linked moesin-associated immunodeficiency all presented with recurrent bacterial infections of the respiratory, gastrointestinal or urinary tracts, and some had severe varicella.Therapeutically, in the absence of a molecular diagnosis and due to his SCID-like phenotype, one patient was treated with geno-identical hematopoietic stem cell transplantation . The remaining are untreated or treated with immunoglobulin substitution and/or prophylactic antibiotics. Since this study, the moesin gene has been integrated into DNA chips used for the molecular diagnosis of immune deficiencies in several countries. Physicians in Canada, the United States, Japan, South Africa and Europe have contacted us with a total of 16 known participants to date. Because of their very low severe, uncontrolled CMV infection and the absence of treatment recommendations, two 2 American participants were treated with allogeneic transplantation with severe post-transplant complications (1), and one of the participants died as a result of the transplant. Management of XMAID participants therefore varies widely from country to country, depending on age at diagnosis and clinical picture. It ranges from no treatment treatment (associated with recurrent infections and skin manifestations), IgIv substitution and/or antibiotic prophylaxis antibiotic prophylaxis, with low toxicity and apparent efficacy, and allogeneic transplantation, with all the risks risks involved (graft-related toxicity, graft versus host, disease, rejection, risk of infection). The Investigators therefore feel it is important to review the diagnosis, clinical presentation and management of X-MAID participants. The study the investigator propose will enable to understand the presentation of X-MAID participants, establish guidelines and provide the best treatment for each patient according to his or her clinical picture


Eligibility

Sex: MALEMin Age: 4 YearsMax Age: 80 Years

Inclusion Criteria2

  • Male patient with a mutation in the MOESIN gene (MSN)
  • No objection to the collection of personal health data

Exclusion Criteria1

  • \-

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

GENETICgenetic restrospective study

it is not an interventional study but observational


Locations(10)

National Institutes of Health

Bethesda, Maryland, United States

Perelman School of medecine

Philadelphia, Pennsylvania, United States

Brown University

Providence, Rhode Island, United States

Genomic Research Centre, School of Biomedical Sciences Institute of Health and Biomedical Innovation

Brisbane, Australia

Hôpital Universitaire de la Reine Fabiola

Brussels, Belgium

Hôpital Necker

Paris, PARIS, France

CHU Rennes, CNRS UMR 629

Rennes, France

CHU St Etienne Hôpital Nord

Saint-Etienne, France

Tokyo Medical and Dental University (TMDU)

Bunkyō City, Japan

Departments of Internal Medicine and Immunology

Rotterdam, Netherlands

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06278337


Related Trials