Human Polyomavirus-Associated Cerebral Disorders in the Post-HAART Era

Author:

Cedeno-Laurent Filiberto1,Penalva de Oliveira Augusto C.23,Vidal José E.4,Trujillo J. Roberto5

Affiliation:

1. Harvard Medical School, Boston, MA 02215, USA

2. Department of Neurology, Institute of Infectious Diseases “Emilio Ribas,” 040088-002, São Paulo, SP, Brazil

3. Unit on Clinical Investigation of Human Retroviruses, Campinas University, São Paulo, Brazil

4. Department of Infectious Diseases, Institute of Infectious Diseases “Emilio Ribas,” 040088-002, São Paulo, SP, Brazil

5. TruBios Research Institute, Johns Hopkins University, MCC, 9605 Medical Center Drive, Suite 105, Rockville, MD 20850, USA

Abstract

Human polyomavirus JC is the causative agent of a deadly form of sudden onset dementia, progressive multifocal leukocoencephalopathy (PML). PML is highly prevalent in immunodeficient populations, specially those undergoing chemotherapy, immunosuppressive treatments for autoimmune conditions, and HIV-1/AIDS patients. In fact, before the highly active antiretroviral therapy (HAART) regimens became available, PML was a leading cause of death in HIV-1 seropositive individuals. However, patients under HAART show increased survival times with better prognoses. In this report we described the main differences between PML before and after the HAART era; highlighting the new patterns of presentation, the neurotropism of other human polyomaviruses, and the increased prevalence of immune reconstitution inflammatory syndrome (IRIS), as a complication of PML in patients under HAART. Lastly, we propose a revised classification of human poliomavirus-associated cerebral disorders that may reflect more accurately what clinicians encounter in their everyday practice.

Publisher

Hindawi Limited

Subject

Pathology and Forensic Medicine

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