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Updated: May 29, 2026

Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
Human herpes virus 8 in solid organ transplantation
Ella J Ariza-Heredia1, Raymund R Razonable
1Division of Infectious Diseases, Mayo Clinic, Rochester, MN 55905, USA. Razonable.raymund@mayo.edu
Human herpes virus 8 (HHV-8) causes cancers like Kaposi's sarcoma, especially in transplant patients. Managing HHV-8 involves reducing immunosuppression, with potential roles for sirolimus and antivirals.
Area of Science:
- Virology
- Oncology
- Immunology
Background:
- Human herpes virus 8 (HHV-8) is geographically restricted, causing neoplastic and nonneoplastic diseases.
- HHV-8 infection establishes lifelong latency, but can reactivate when host immunity is compromised, such as post-organ transplantation.
- Kaposi's sarcoma, primary effusion lymphoma, and Castleman's disease are the main malignancies linked to HHV-8.
Purpose of the Study:
- To review the association between HHV-8 and neoplastic diseases, particularly in organ transplant recipients.
- To discuss the risk factors, clinical manifestations, and management strategies for HHV-8-associated malignancies.
- To highlight the current gaps in HHV-8 screening and treatment in the transplant setting.
Main Methods:
- Literature review of HHV-8 epidemiology, pathogenesis, and clinical associations.
- Analysis of HHV-8 prevalence and disease incidence in endemic versus low-prevalent regions.
- Examination of current and potential therapeutic approaches for HHV-8-related conditions.
Main Results:
- Neoplastic disease incidence mirrors HHV-8 seroprevalence, with highest risk in immunocompromised individuals, especially solid organ transplant recipients from endemic areas.
- Transplant recipients may develop Kaposi's sarcoma, primary effusion lymphoma, or Castleman's disease following HHV-8 reactivation or primary infection.
- No standard HHV-8 screening exists for transplant patients; HHV-8 PCR confirms clinical suspicion.
Conclusions:
- Management focuses on reducing immunosuppression; chemotherapy may be needed.
- Sirolimus shows potential due to antiproliferative properties; the role of antivirals is undefined.
- Further research is needed to establish screening protocols and define the role of antiviral therapy for HHV-8 in transplant recipients.
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