Human T-cell lymphotropic virus type I (HTLV-I) is known to cause adul
t T-cell leukemia/T-cell lymphoma and tropical spastic paraparesis/HTL
V-I-associated myelopathy. Recent seroepidemiologic, clinical, and vir
ologic studies indicate that the virus is also related to a certain ty
pe of uveitis, which has been classified as uveitis without defined et
iologies or idiopathic uveitis. According to the seroepidemiologic sur
vey, the seroprevalence of HTLV-I in patients with idiopathic uveitis
was significantly higher than that of two control groups, that is, pat
ients with uveitis with defined etiologies and patients with nonuveiti
c ocular diseases, Clinically, the uveitis seen in HTLV-I carriers is
characterized by moderate to severe cellular infiltration in the eye a
nd by moderate retinal vasculitis, and the intraocular inflammation re
sponds well to corticosteroid therapy. Interestingly, 25% of female pa
tients with the disease had a previous history of Graves disease with
hyperthyroidisms. The following virologic, molecular biologic findings
suggest that cytokines produced by HTLV-I-infected T cells in the eye
play the central role in the pathogenic mechanisms of the uveitis: (a
) the virus load in the peripheral blood monocytes analyzed by the qua
ntitative polymerase chain reaction methods was significantly greater
in patients with the uveitis than in asymptomatic carriers, (b) the pr
oviral DNA of HTLV-I and the gene expression of the virus at the mRNA
level was detected in the infiltrating cells from the eyes of the pati
ents, (c) the virus particles were detected by electron-microscopic ex
amination in the T-cell clones established from the intraocular fluid
of the patients, and (d) the HTLV-I-infected T cells produced a variet
y of cytokines without any stimuli, such as interleukin (IL)-1 alpha,
IL-2, IL-3, IL-6, IL-8, IL-10, tumor necrosis factor alpha, interferon
-gamma, and granulocyte-macrophage colony-stimulating factor, Based on
the seroepidemiologic, clinical, and virologic data, the uveitis seen
in HTLV-I carriers is considered to be a distinct clinical entity rel
ated to HTLV-I infection, and the disease is designated as HTLV-I uvei
tis.