Medical Care in China

Myelitis spectrum disorders (neuromyelitis optica spectrum disorder NMOSD, etc.)
Treatment in China

Provide a clear and complete coordinated pathway from expert assessment to treatment and rehabilitation.

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Multidisciplinary consultationsinvolving joint analysis of complex cases by different specialties.
Accurately identify the cause of the diseaseby combining imaging, laboratory and genetic testing.
Tackling complex casesFocusing on Relapsed, Refractory, and Poorly Treated Cases.
Personalized plans aredeveloped based on the patient's actual condition to create a treatment pathway.

Condition Guide

About Myelitis spectrum disorders (neuromyelitis optica spectrum disorder NMOSD, etc.)

Understand the condition, common triggers and treatment options that may require specialist assessment.

Disease Introduction

Neuromyelitis spectrum optica disorder (NMOSD) is a rare autoimmune disease of the central nervous system, often caused by the production of anti-aquaporin 4 antibodies (AQP4-IgG) that mistakenly attack the optic nerve and spinal cord. Symptoms include decreased vision, numbness and weakness in the limbs, hiccups and vomiting, and bowel and bladder dysfunction. Recurrent attacks can lead to blindness or paralysis. The disease is more common in young adult women; early diagnosis and treatment, and adherence to remission periods to prevent relapse, are crucial for preserving neurological function.

Cutting-edge high-precision diagnostic and treatment technologies

  1. Oxtuzumab β : Betuzumab® is a domestically produced third-generation CD20 monoclonal antibody. It was approved for marketing by the NMPA in February 2026. The Phase III study showed that the risk of relapse in AQP4-IgG positive patients was reduced by 97.9% compared with placebo, with an annualized relapse rate of only 0.025 times/person-year. The results were published in Nature Medicine.
  2. Inelizumab : The world's first CD19-targeting B-cell depletion agent, approved in China in March 2022 for the treatment of adult NMOSD with anti-AQP4 antibody positivity, continuously reducing the relapse rate, and included in the National Reimbursement Drug List in 2023.
  3. Eculizumab : Approved in China in October 2023 for the treatment of AQP4 antibody-positive NMOSD in adults. It is currently the only approved complement C5 inhibitor in China, which blocks optic nerve and spinal cord inflammation caused by terminal complement cascade.
  4. Saturizumab : Approved in China in April 2021 for AQP4 antibody-positive NMOSD in children ≥12 years old. It is a subcutaneous anti-IL-6 receptor monoclonal antibody that inhibits pro-inflammatory cytokine pathways from the source and reduces the risk of relapse.
  5. Relizumab : A long-acting complement C5 inhibitor is undergoing a Phase IIIb clinical trial in China for adult NMOSD, which further improves the convenience of long-term

Care Overview

Myelitis spectrum disorders (neuromyelitis optica spectrum disorder NMOSD, etc.) Treatment in China

The medical team will develop a personalized protocol based on the pathology type, stage, genetic test, previous treatment history, and the patient's physical condition.

Leading Specialists

Trusted Expertise Across Leading Specialties

Wanping

Associate Chief Physician, Liver Surgery Expert at Renji Hospital.

Rare & Complex Diseases

Research Areas : Pediatric liver transplantation, Kasai procedure for biliary atresia, and complex liver tumor resection, among other pediatric liver surgeries. Cutting-Edge Techniques: Proficient in the surgical treatment of pediatric liver diseases such as biliary atresia, inherited metabolic diseases, cholestasis, and hepatoblastoma, having treated over 1700 cases of various pediatric liver diseases and rare diseases; as a core member of the team, systematically conducting liver transplantation surgery

West China Hospital of Sichuan University logo Affiliated Hospital West China Hospital of Sichuan University
Wu Yu

Chief Physician, Doctoral Supervisor, specializing in rare hematological diseases

Rare & Complex Diseases

Research areas : rare hematological diseases, hereditary hemolytic diseases, systemic amyloidosis - Cutting-edge technologies: Stratified treatment for systemic amyloidosis, molecular diagnostics for complex hematological and rare diseases. - Areas of expertise: Systemic AL amyloidosis, paroxysmal nocturnal hemoglobinuria, hereditary platelet disorders - Academic Highlights: Core expert in multidisciplinary diagnosis and treatment of amyloidosis in China; Core Value: Establishment of individualized drug a

West China Hospital of Sichuan University logo Affiliated Hospital West China Hospital of Sichuan University
Zhang Shuyang

President of Peking Union Medical College Hospital, and concurrently Vice President of the Chinese Academy of Medical Sciences and Peking Union Medical College; Chief Physician, Dr., and Doctoral Supervisor

Rare & Complex Diseases

Deputy Director of the State Key Laboratory of Rare and Complex Diseases; National Health Commission Outstanding Young and Middle-aged Expert, State Council Special Government Allowance Expert, and Changjiang Scholar Dr. appointed by the Ministry of Education. Currently serves as Chairman of the Rare Diseases Branch of the Chinese Medical Association, Chairman of the Rare Disease Diagnosis and Treatment and Guarantee Committee of the National Health Commission, Director of the National Rare Disease Qualit

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences logo Affiliated Hospital Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Shen Min

Doctor of Medicine, Director of the Department of Rare Diseases, Chief Physician of Rheumatology and Immunology, Dr., and Doctoral Supervisor at Peking Union Medical College Hospital.

Rare & Complex DiseasesInternal Medicine

Visiting Scholar at the University of California, San Francisco, and Visiting Researcher in Rheumatology and Immunology at the Cleveland Clinic. Editorial Board Member of the *Chinese Journal of Clinical Immunology and Allergy*, *Chinese Journal of General Practitioners*, and *Peking Union Medical College Journal*. Vice Chairman of the Immunodeficiency Monitoring and Translation Professional Committee of the China Association for the Promotion of Human Health Science and Technology; Standing Committee Mem

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences logo Affiliated Hospital Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Zhang Guojun

Chief Physician, Dr., and Doctoral Supervisor. Currently serves as Director of the Neurology Center, Epilepsy Center, Rare Disease Center, and Neurological Diseases and Cognitive Research Laboratory at the National Children's Medical Center and Beijing Children's Hospital, Capital Medical University.

NeurologyRare & Complex Diseases

Has extensive clinical experience in the surgical treatment of functional neurosurgical diseases, especially refractory epilepsy, and has long been engaged in research on the pathogenesis and intervention strategies of epilepsy and cognitive developmental disorders. Graduated from the Department of Medicine, Hebei Medical University in 1989, and received a Ph.D. in Surgery (Neurosurgery) from Capital Medical University in 2003. Has undertaken more than ten national and provincial-level research projects a

Beijing Children's Hospital (School of Pediatrics, National Children's Medical Center), Capital Medical University logo Affiliated Hospital Beijing Children's Hospital (School of Pediatrics, National Children's Medical Center), Capital Medical University

Patient Stories

See the Next Step Through Patient Journeys

Adult Still's Disease : The End of 120 Days of CASE 01
PATIENT JOURNEY

Adult Still's Disease : The End of 120 Days of "Unexplained High Fever": How a British Pilot Regains His Career in China

Rare & Complex Diseases

Patient records Name: James (pseudonym) Age: 35 Nationality: British Diagnosis: Adult-onset Still's disease (AOSD), characterized by a triad of high fever, rash, and arthritis, accompanied by severe ferritinemia. Treatment Hospital: Department of Rheumatology and Immunology, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine For a pilot, any undiagnosed illness means the end of his career. James' nightmare began with what seemed like a common cold, but turned into a 120-day ord

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IgG4-related disease (involving the pancreas, submandibular gland, and retroperitoneal lymph nodes) - Two years shrouded in CASE 02
PATIENT JOURNEY

IgG4-related disease (involving the pancreas, submandibular gland, and retroperitoneal lymph nodes) - Two years shrouded in "tumor": How a Canadian patient overturned a wrong diagnosis in China.

Rare & Complex Diseases

Patient records Name: Margaret (pseudonym) Age: 61 Nationality: Canadian Diagnosis: IgG4-related disease (involving the pancreas, submandibular gland, and retroperitoneal lymph nodes), previously misdiagnosed as pancreatic cancer. Treatment Hospital: Department of Rheumatology and Immunology, Peking Union Medical College Hospital Case Theme: In the world of intractable diseases, the most agonizing part is often not the treatment itself, but the journey further and further down the path of treatment with a

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