In 1985 we had the first indication that human T-cell lymphotropic vir
us (HTLV-I) was the possible etiological agent of a chronic myelopathy
that seemed to be peculiar to the tropics and that is now known as en
demic tropical spastic paraparesis (TSP). IgG antibodies to HTLV-I wer
e found in serum and cerebrospinal fluid of patients from Jamaica, Col
ombia, Martinique, and shortly after in southern Japan, where the dise
ase is called HTLV-I-associated myelopathy (HAM). The HTLV-I seroposit
ivity was first determined by enzyme-linked immunoassay and confirmed
by western immunoblot and in the cerebrospinal fluid specific IgG olig
oclonal bands to HTLV-I were found in cerebrospinal fluid and not in s
erum. These laboratory findings indicated that HTLV-I could be neuropa
thogenic and for the first time a single etiological agent was identif
ied in patients from different countries. Thus, in less than a decade
a century of research and speculation was seemingly resolved when this
disease, which was thought to occur only in blacks of poor socieconom
ic status in tropical countries, was shown to occur in all ethnic grou
ps of varying socioeconomic status in temperate, subtropical, and trop
ical climates.