HTLV‐I/II Seroindeterminate Western Blot Reactivity in a Cohort of Patients with Neurological Disease
Author(s) -
Samantha S. Soldan,
Michael D. Graf,
Allen Waziri,
Alfred N. Flerlage,
Susan M. Robinson,
Taketo Kawanishi,
Thomas Leist,
Tanya Lehky,
Michael C. Levin,
Steven Jacobson
Publication year - 1999
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/314923
Subject(s) - tropical spastic paraparesis , western blot , virology , retrovirus , immunology , virus , blot , human t lymphotropic virus , biology , antibody , medicine , myelopathy , gene , genetics , neuroscience , spinal cord
The human T-cell lymphotropic virus type I (HTLV-I) is associated with a chronic, progressive neurological disease known as HTLV-I-associated myelopathy/tropical spastic paraparesis. Screening for HTLV-I involves the detection of virus-specific serum antibodies by EIA and confirmation by Western blot. HTLV-I/II seroindeterminate Western blot patterns have been described worldwide. However, the significance of this blot pattern is unclear. We identified 8 patients with neurological disease and an HTLV-I/II seroindeterminate Western blot pattern, none of whom demonstrated increased spontaneous proliferation and HTLV-I-specific cytotoxic T lymphocyte activity. However, HTLV-I tax sequence was amplified from the peripheral blood lymphocytes of 4 of them. These data suggest that patients with chronic progressive neurological disease and HTLV-I/II Western blot seroindeterminate reactivity may harbor either defective HTLV-I, novel retrovirus with partial homology to HTLV-I, or HTLV-I in low copy number.
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