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Exploratory Study on Unknown Antibodies in Neuroimmune Diseases

Exploratory Study on Unknown Antibodies in Neuroimmune Diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129097
Enrollment
Unknown
Registered
2026-07-30
Start date
2026-07-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Neuroimmune disorders such as autoimmune encephalitis, neuromyelitis optica spectrum disorders, myasthenia gravis, and immune-mediated peripheral neuropathy

Interventions

Sponsors

Punan Hospital,Pudong New District, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnostic criteria: The clinical manifestations, cerebrospinal fluid, imaging findings, and immune treatment responses strongly support neuroantibody-mediated autoimmune diseases, including autoimmune encephalitis, neuromyelitis optica spectrum disorders, myasthenia gravis, and immune-mediated peripheral neuropathy, etc.; 2. Inclusion criteria: The results of routine + broad-spectrum + rare neuroantibody tests are all negative; Serum/plasma exchange fluid (=10ml) can be provided, and cerebrospinal fluid can be provided as well; 3. Those who can provide dynamic samples before, during, and after treatment are preferred for inclusion; The samples should be stored under standard conditions at -80?, without repeated freezing, hemolysis, or degradation; The clinical diagnosis and treatment data are complete, the background is clear, and they can meet the subsequent verification requirements.

Exclusion criteria

Exclusion criteria: 1. The diagnosis was made as non-immune neurological diseases such as infection, tumor, genetics, metabolism, poisoning, vascular, and traumatic disorders; 2. The samples were repeatedly frozen and thawed, hemolyzed, contaminated, or insufficient in quantity, making it impossible to complete the experiments; 3. The clinical data were severely lacking, making it impossible to determine the possibility of an immune cause; 4. After extensive antibody spectrum screening, it was confirmed as a positive result for known antibodies; 5. Dynamic samples before and after treatment could not be provided, or the ethical and informed consent was incomplete.

Design outcomes

Primary

MeasureTime frame
Novel neural autoantibody detection rate;TBA positivity rate;Candidate antigen validation success rate;

Secondary

MeasureTime frame
Association between antibodies and clinical phenotypes, treatment response, and prognosis;Dynamic changes in antibody levels before and after treatment;

Countries

China

Contacts

Public ContactGuan Yangtai

Punan Hospital,Pudong New District, Shanghai

qiujuli2019@163.com+86 21 20302000

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026