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Prospective, one-arm study of immunosorbent therapy for disseminated infection associated with anti-interferon-? autoantibody immune deficiency syndrome

Prospective, one-arm study of immunosorbent therapy for disseminated infection associated with anti-interferon-? autoantibody immune deficiency syndrome

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094451
Enrollment
Unknown
Registered
2024-12-23
Start date
2024-05-07
Completion date
Unknown
Last updated
2025-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

anti-interferon-? autoantibody immune deficiency syndrome

Interventions

Test group:Immunosorbent therapy

Sponsors

The Third Affiliated Hospital Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. >=18 years of age; 2. HIV antibody negative; 3. No glucocorticoids, immunosuppressants, immunocytotoxic biologics, and antitumor drugs were used in the whole body within 1 year; 4. No other active autoimmune disease or uncured malignancy; 5. Primary immunodeficiency disease has not been diagnosed; 6. Any one or more of the following infectious diseases were diagnosed at the time of admission: disseminated Marneffei basiomycosis, disseminated tuberculosis, disseminated nontuberculous mycobacterium infection, disseminated cryptococcosis, disseminated nocardia infection, disseminated histoplasmosis, disseminated nontyphoid salmonella infection, etc.; 7. AIGAs positive in peripheral blood.

Exclusion criteria

Exclusion criteria: 1. Severe active bleeding or disseminated intravascular coagulation at the time of enrollment; 2. Hemodynamic instability such as shock and malignant arrhythmia; 3. Severe allergies to plasma, heparin, protamine, etc.; 4. Acute stage of myocardial infarction and cerebral infarction; 5. Other cases that do not agree or do not cooperate with immunosorbent therapy.

Design outcomes

Primary

MeasureTime frame
The period of remission of a patient's disseminated infection;

Secondary

MeasureTime frame
AIGAs;clinical index;Image index;Thrombotic event;Physicochemical index;

Countries

China

Contacts

Public ContactJing Liu

The Third Affiliated Hospital Sun Yat-sen University

liuj26@mail.sysu.edu.cn+86 20 85252372

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026