Human T-Lymphotrophic Virus Types I, II - HTLV I, II
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Algorithm(s)
PDF algorithm(s) available at www.arupconsult.com.
Human T-Lymphotrophic Virus Types I and II Testing Algorithm

Clinical Background

HTLV-I is etiologically associated with adult T-cell leukemia/lymphoma (ATLL), a demyelinating neurological disorder termed tropical spastic paraparesis (TSP) and with HTLV-I associated myelopathy (HAM).

Epidemiology

  • Prevalence - 15-20 million globally infected with HTLV-I
    • Endemic in Japan, Caribbean countries and Sub-Saharan Africa
  • Age - median age is 50s
    • HAM/TSP - 4th to 5th decade
  • Sex
    • ATLL - M>F
    • HAM/TSP - F>M
  • Transmission
    • Parenteral
    • Sexual

Organism

  • HTLV-I and HTLV-II are human type C retroviruses
    • Several subtypes exist that are geographically specific
  • Majority of human infections is caused by subtype 1
  • HTLV and AIDS
    • HTLV-I does not cause AIDS
    • Antibodies of HTLV-I have no relationship to antibodies of HIV-I, and antibodies to HTLV-I do not imply excess risk for AIDS
    • HTLV-I virus is only remotely related to AIDS virus, HIV-I
    • HTLV-I and HTLV-II are transmitted similarly to HIV-I and HIV-II
    • Individuals with HTLV-I or HTLV-II may be coinfected with HIV due to common risk factors (sexual contact, intravenous drug use)

Risk Factors

  • Cellular blood products - most efficient mode of transmission
  • Breast milk - 20% of children of infected mothers will also become infected
  • Sexual contact - associated with unprotected sex, multiple partners, presence of genital sores, sex exchanged for drugs or money
  • Sharing of contaminated needles and syringes (intravenous drug users)
  • Suspicion of perinatal transmission
  • Poverty

Clinical Presentation

  • ATLL
    • Life-time risk for ATLL in those with HTLV-I antibodies is low;
      • Even in countries with a high prevalence of HTLV-I (eg, Japan), the risk for developing ATLL is only 1-2%
    • 4 types of ATLL - acute, chronic, smoldering, lymphoma
    • Acute ATLL most common
      • Rapidly fatal without treatment
      • Pulmonary complications, opportunistic infections, sepsis
      • Uncontrolled hypercalcemia may occur
  • HAM/TSP
    • Slowly progressive spastic paraparesis
    • Develops in up to 4% of infected patients
    • Caused by immune response to HTLV-I
See Also
  Acute Myelogenous Leukemia - AML
  Chronic Myelogenous Leukemia - CML
  Leukemia Lymphoma Phenotyping
  Neuropathic Disease
  Paraneoplastic Neurological Syndromes

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