The human T-cell leukemia virus HTLV-1—also known as human T-lymphotropic virus type 1—was the first human retrovirus discovered. Unlike HIV-1, it has been present in humans for tens of thousands of years, and in consequence HTLV-1 is exquisitely adapted to persist in the individual host. Its life history therefore differs fundamentally from that of HIV-1 in key respects. HTLV-1 causes an aggressive hematological malignancy known as adult T-cell leukemia-lymphoma (ATL) and a progressive inflammatory disease of the central nervous system, HTLV-1-associated myelopathy (HAM), in a proportion of infected people. These conditions impose a significant health burden in countries where the virus is endemic.
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Bangham et al. (2026) studied this question.
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