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Updated: Jul 17, 2025

An Efficient and Simple Method to Establish NK and T Cell Lines from Patients with Chronic Active Epstein-Barr Virus Infection
Published on: March 30, 2018
A successful treatment for chronic active Epstein-Barr virus disease with Nephrotic Syndrome
Yasuhiro Inaba1, Akinori Miyazono2, Kenichi Imadome3
1Department of Pediatrics, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima City, 890-8520, Japan. y-i-0602@m2.kufm.kagoshima-u.ac.jp.
Insights
Chronic active Epstein-Barr virus (CAEBV) disease can occur during immunosuppressive therapy. Reducing immunosuppressive drug dosage, without chemotherapy or stem cell transplant, effectively controlled CAEBV and the primary condition.
Area of Science:
- Immunology
- Virology
- Pediatrics
Background:
- Chronic active Epstein-Barr virus (CAEBV) disease presents a poor prognosis without treatment like hematopoietic stem cell transplantation (HSCT).
- Standard treatments including chemotherapy and HSCT are challenging to maintain and have limited long-term efficacy.
- CAEBV can arise in patients undergoing immunosuppressive therapy for other conditions, complicating treatment options.
Observation:
- A 13-year-old boy developed CAEBV while on cyclosporine A (CyA) for steroid-dependent nephrotic syndrome (SDNS).
- HSCT and chemotherapy were not viable options due to the patient's SDNS.
- The patient's immunosuppressed state was hypothesized to contribute to CAEBV, prompting a gradual reduction in CyA dosage.
Findings:
- Reducing the CyA dose was carefully managed to balance T-cell immunity activation and control of both CAEBV and SDNS.
- The adjusted CyA dosage successfully suppressed both CAEBV disease and SDNS for over nine years.
- This approach demonstrated that dose reduction of immunosuppressive agents can be effective without resorting to chemotherapy or HSCT.
Implications:
- This case report introduces a novel treatment strategy for CAEBV in immunosuppressed patients.
- Reducing immunosuppressive drug dosage offers a viable alternative when standard treatments are contraindicated or ineffective.
- Further research into optimizing immunosuppressive drug tapering for managing CAEBV is warranted.
Abstract:
Chronic active Epstein-Barr virus (CAEBV) disease is more likely to occur when a patient is on immunosuppressive therapy for any disease or is susceptible to infection, and the prognosis is poor without appropriate treatment, including hematopoietic stem cell transplantation (HSCT). In addition to HSCT, several other chemotherapy regimens have been reported, but all of them are difficult to maintain in remission. Without HSCT, survival rates have been reported to be 50% in 5 years and 25% in 15 years. This is a report of a 13-year-old boy who developed CAEBV disease during cyclosporine A (CyA) treatment for the steroid-dependent nephrotic syndrome (SDNS). Since SDNS precluded HSCT or chemotherapy, CyA was tapered off based on the belief that alleviating his immunosuppressed state would decrease the CAEBV disease. We decided to gradually reduce the CyA dose to activate T-cell immunity, while periodically monitoring the EBV viral load. Finally, we found an appropriate dose that could suppress both CAEBV disease and SDNS, and it lasted for more than 9 years. No case has been reported to date in which a patient developed CAEBV disease while receiving immunosuppressive drugs for the primary disease, and both diseases were controlled only by reducing the dose of immunosuppressive drugs. In this report, we show that dose reduction of immunosuppressive agents without chemotherapy or HSCT is an effective option for the treatment of CAEBV disease in patients receiving immunosuppressive agents.
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