HTLV-1-associated diseases: a systematic review

Autores/as

  • Rosa Maria Nascimento Marcusso Instituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil
  • Víctor Ângelo Folgosi Universidade de São Paulo, Faculdade de Medicina, Divisão de Dermatologia, Laboratório de Investigação Médica (LIM-56), São Paulo, São Paulo, Brazil
  • Augusto César Penalva de Oliveira Instituto de Infectologia Emilio Ribas, São Paulo, São Paulo, Brazil
  • Jorge Casseb Universidade de São Paulo, Faculdade de Medicina, Divisão de Dermatologia, Laboratório de Investigação Médica (LIM-56), São Paulo, São Paulo, Brazil; Universidade de São Paulo, Faculdade de Medicina, Instituto de Medicina Tropical de São Paulo, São Paulo, São Paulo, Brazil

DOI:

https://doi.org/10.1590/S1678-9946202668054

Palabras clave:

HTLV-1, HAM/TSP, Adult T-cell Leukemia/Lymphoma, Proviral load, Inflammatory diseases

Resumen

Human T-cell lymphotropic virus type 1 (HTLV-1) is a human retrovirus associated with a broad spectrum of clinical manifestations. While most people living with HTLV-1 remain asymptomatic, a proportion develops severe conditions such as adult T-cell leukemia/lymphoma or HTLV-1-associated myelopathy/tropical spastic paraparesis. Increasing evidence also indicates that HTLV-1 infection is related to multiple systemic complications involving different organ systems (including neurological, pulmonary, dermatological, rheumatological, and ophthalmological disorders) and opportunistic infections. Given the growing recognition of these diverse manifestations, this review aims to compile and synthesize the scientific evidence regarding clinical manifestations, co-infections, opportunistic diseases, and complications related to HTLV-1 infection.

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Publicado

2026-08-11

Número

Sección

Review

Cómo citar

Marcusso, R. M. N., Folgosi, V. Ângelo, Oliveira, A. C. P. de, & Casseb, J. (2026). HTLV-1-associated diseases: a systematic review. Revista Do Instituto De Medicina Tropical De São Paulo, 68, e54. https://doi.org/10.1590/S1678-9946202668054

Datos de los fondos