Jj. Lefrere et al., Natural history of the TT virus infection through follow-up of TTV DNA-positive multiple-transfused patients, BLOOD, 95(1), 2000, pp. 347-351
Little is known about the natural history and the pathogenicity of the TT v
irus (TTV). We present our findings of a cross-sectional study based on the
TTV DNA screening of 173 multiple-transfused patients and a longitudinal s
tudy based on the follow-up of TTV DNA-positive patients. Overall, 48 patie
nts (27.7%) tested positive for TTV DNA. The influence of the number of blo
od donor exposures on the prevalence of bloodborne viral infection indicate
s that TTV, hepatitis C virus (HCV), and an RNA virus known as GB virus C/h
epatitis G virus (GBV-C/HGV) share a parenteral transmission, but that TTV,
in contrast to the 2 other viruses, is also transmitted by at least anothe
r efficient means. The patients having a well-defined date of TTV infection
were positive for TTV DNA during a mean period of 3.1 years. A chronic inf
ection was observed in 31 cases (86%), TTV carriage appeared clinically ben
ign in all patients. No clinical evidence of a disease potentially linked t
o the TTV infection was observed in patients with TTV DNA carriage over sev
eral years. The majority of TTV carriers had no biochemical evidence of liv
er disease. The prevalence of elevated serum alanine aminotransferase (ALT)
level was higher in the TTV DNA-positive group, even in the absence of HCV
infection, but the observed peaks of ALT level were most often transient a
nd very mild. The prevalence of TTV DNA observed in blood recipients is con
sistent with that of TTV infection observed in blood donors. TTV infection
frequently tends to persist. (C) 2000 by The American Society of Hematology
.