BACKGROUND: Recently, cases of chronic hepatitis were linked to the pr
esence of genomic sequences of a newly described RNA virus termed hepa
titis G virus (HGV) and belonging to the Flaviviridae family. STUDY DE
SIGN AND METHODS: The presence of HGV RNA was searched for by polymera
se chain reaction in a population of blood donors and in patients who
had received multiple blood component transfusions and/or intravenous
immunoglobulin (IVIG) infusions. RESULTS: Twenty-one (4.2%) of 500 don
ors were positive for HGV RNA as were 21 (10.7%) of 196 nonimmunosuppr
essed patients who had received multiple transfusions of packed red ce
lls, 4 (8.7 %) of 46 common variable immune deficiency (CVID) patients
who had received only IVIG, and 22 (24.7%) of 89 bone marrow transpla
nt (BMT) patients who had received IVIG and cellular components. The p
roportion of HGV-positive individuals was significantly higher in the
immunosuppressed recipients (CVID and BMT patients) than in the nonimm
unosuppressed patients who were multiply transfused with packed red ce
lls (p<0.03). The proportion of HGV-positive individuals was significa
ntly higher in the BMT patients who had received IVIG and cellular com
ponents than in the CVID patients who had received IVIG only (p<0.03).
Eight (17.0%) of the 47 HGV-positive recipients and 48 (16.9%) of the
284 HGV-negative recipients had a serum alanine aminotransferase leve
l higher than the upper limit of normal (nonsignificant difference). T
he medical history of HGV-positive donors failed to reveal a particula
r at-risk event. The targe majority of HGV-infected patients had a nor
mal serum alanine aminotransferase level, and the proportion of patien
ts with elevated alanine aminotransferase was the same in HGV-positive
and in HGV-negative recipients. CONCLUSION: The pathological signific
ance of HGV infection remains unelucidated, and the classification of
HGV as a new hepatitis virus was perhaps premature.