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The theory and related mechanism of ''immune-inflammatory reconstitution'' in immunosuppressed host-kidney transplant recipients

The theory and related mechanism of ''immune-inflammatory reconstitution'' in immunosuppressed host-kidney transplant recipients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100049261
Enrollment
Unknown
Registered
2021-07-28
Start date
2021-07-31
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Immunocompromise after transplantation

Interventions

patient group:None
control group:None

Sponsors

Zhongshan Hospital Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Group of patients receiving kidney transplantation: (1) Aged >= 18 years, gender is not limited; (2) End-stage renal disease meets the criteria for kidney transplantation, and receives primary allogeneic kidney transplantation; (3) Not receiving any immunomodulatory therapy before receiving transplantation; (4) Accept standard triple immunosuppression regimen after transplantation, namely CNI (cyclosporine/tacrolimus) + MPA (mycophenolate mofetil/mycophenolate sodium enteric-coated tablet) + glucocorticoid; (5) Obtain informed consent and sign an informed consent form. 2. Healthy control group: (1) Aged >= 18 years, gender is not limited; (2) No chronic underlying diseases and no immunosuppressive agents; (3) No infectious disease in the past 1 month; (4) Obtain informed consent and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with co-infection before a clear diagnosis; 2. Patients with tumors, blood system diseases, rheumatic immune system diseases, and HIV diseases; 3. Patients who have received solid organ transplantation other than kidney; 4. Patients with uncontrollable neurological, mental diseases or mental disorders, poor compliance and unable to cooperate; 5. Patients who have joined other clinical trials.

Design outcomes

Primary

MeasureTime frame
Immune cell subsets;

Countries

China

Contacts

Public ContactKuang Zhongshu

Zhongshan Hospital Fudan University

kuangzhongshu714@163.com+86 15026867439

Outcome results

None listed

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