X-linked Moesin Associated Immunodeficiency

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age4-80
SponsorInstitut National de la Santé Et de la Recherche Médicale, France

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Male patient with a mutation in the MOESIN gene (MSN)

No objection to the collection of personal health data

Disqualifiers

None

Trial population

Given the small number of participants and the purpose of the study, the group may include deceased patients (at least 1 of the 16 participants). The sample size is 16 patients already identified, and possibly other patients who may be identified once the existence of the the existence of the international registry. Final enrolment will correspond to all X-MAID patients diagnosed worldwide who agree to take part in the study.

Trial design

Design model

Other

Time perspective

Retrospective

Treatments tested in this trial

  • genetic restrospective study

    Genetic

    it is not an interventional study but observational

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

The main objective

The main objective is to study the clinical results of the different therapeutic options applied to X-MAID patients, and to investigate whether there is a correlation between treatment responses and mutation position

Time frame
through study completion, and average 3 years

Secondary outcomes

1

Secondary objectives1

Circumstances of genetic diagnosis: at what age are these patients diagnosed, and by what means? (role of prenatal screening).

Time frame
through study completion, and average 3 years

Other outcomes

1

secondary objectives 2

What is the state of their immune system and, depending on this state, the CID or SCID classification of the disease.

Time frame
through study completion, and average 3 years
2

secondary objective 3

What are the clinical manifestations of the disease (cutaneous, infectious, autoimmune)?

Time frame
All the patients are male. As a result of their immune deficiency, patients suffer from recurrent bacterial infections of the respiratory, digestive and urinary tracts, as well as, in some cases, skin manifestations such as eczema, alopecia and molluscum
3

secondary objectives 4

What impact does the disease have on their development?

Time frame
Among patients diagnosed in the first years of life, none showed developmental defects.
4

secondary objective 5

What are the treatments and their consequences?

Time frame
Treatments range from no prophylaxis at all to antibiotic prophylaxis, with or without immunoglobulin therapy, granulocyte-colony-stimulating factor therapy or hematopoietic stem cell allograft.

Sponsors and contacts

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