Serological, epidemiological, and molecular differences between human T-cell lymphotropic virus type 1 (HTLV-1)-Seropositive healthy carriers and persons with HTLV-I gag indeterminate western blot patterns from the Caribbean
F. Rouet et al., Serological, epidemiological, and molecular differences between human T-cell lymphotropic virus type 1 (HTLV-1)-Seropositive healthy carriers and persons with HTLV-I gag indeterminate western blot patterns from the Caribbean, J CLIN MICR, 39(4), 2001, pp. 1247-1253
To investigate the significance of serological human T-cell lymphotropic vi
rus type 1 (HLTV-1) Gag indeterminate Western blot (WB) patterns in the Car
ibbean, a 6-year (1993 to 1998) cross-sectional study was conducted with 37
,724 blood donors from Guadeloupe (French West Indies), whose sera were rou
tinely screened by enzyme immunoassay (EIA) for the presence of HTLV-1 and
-2 antibodies. By using stringent WE criteria, 77 donors (0.20%) were confi
rmed HTLV-1 seropositive, whereas 150 (0.40%; P < 0.001) were considered HT
LV seroindeterminate. Among them, 41.3% (62) exhibited a typical HTLV-1 Gag
indeterminate profile (HGIP). Furthermore 76 (50.7%) out of the 150 HTLV-s
eroindeterminate subjects were sequentially retested, with a mean duration
of follow-up of 18.3 months (range, 1 to 70 months). Of these, 55 (72.4%) w
ere still EIA positive and maintained the same WE profile whereas the other
s became EIA negative. This follow-up survey included 33 persons with an HG
IP. Twenty-three of them (69.7%) had profiles that did not evolve over time
. Moreover, no case of HTLV-1 seroconversion could be documented over time
by studying such sequential samples. HTLV-1 seroprevalence was characterize
d by an age-dependent curve, a uniform excess in females, a significant rel
ation with hepatitis B core (HBc) antibodies, and a microcluster distributi
on along the Atlantic coast of Guadeloupe. In contrast, the persons with an
HGIP were significantly younger, had a 1:1 sex ratio, did not present any
association with HBc antibodies, and were not clustered along the Atlantic
facade. These divergent epidemiological features, together with discordant
serological screening test results for subjects with HGIP and with the lack
of HTLV-1 proviral sequences detected by PCR in their peripheral blood mon
onuclear cell DNA, strongly suggest that an HGIP does not reflect true HTLV
-1 infection. In regard to these data, healthy blood donors with HGIP shoul
d be reassured that they are unlikely to be infected with HTLV-1 or HTLV-2.