There are two human polyomaviruses, JC virus (JCV) and BK virus (BKV).
Most of the population is infected with these viruses at an early age
and the viruses can persist indefinitely without known adverse effect
s in immunocompetent individuals. There are conflicting reports whethe
r these two viruses are latent in the central nervous system or are re
stricted initially to the renal system. Both JCV and BKV, together wit
h the simian polyomavirus simian virus 40 (SV40), have been associated
with central nervous system disease. In particular, JCV is associated
with the demyelinating disease progressive multifocal leukoencephalop
athy (PML) which was once considered only a rare complication of immun
osuppression in transplant recipients. With the advent of the AIDS pan
demic, PML has become of increasing importance and is now considered r
esponsible for the death of 4% of HIV-infected individuals. Both BKV a
nd SV40 have been detected in the human central nervous system, but th
ere is still controversy on what correlation, if any, these two viruse
s have with disease. Current research has focused on the epidemiology
and pathogenesis of polyomavirus infections to try to understand the r
e-activation process in immunosuppressed individuals. This will lead t
o improvements in the differential diagnosis and treatment of PML. Fur
ther analysis of other neurological complications, to see what role po
lyomavirus plays in these infections, are required. (C) 1998 Chapman &
Hall.