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Published on: November 14, 2016
Subacute progression of human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis
Marco A Lima1, Ramza C Harab, Doris Schor
1The Reference Center on Neuroinfections and HTLV, Instituto de Pesquisa Clínica Evandro Chagas (IPEC), Fundação Oswaldo Cruz, Avenida Brasil 4365, Rio de Janeiro, RJ, Brazil. mlima@ipec.fiocruz.br
Abstract:
Although human T-lymphotropic virus type I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is usually described as a chronic disabling disease, a rapid course over months or even weeks has been reported in some patients. The authors describe the clinical features of HAM/TSP in a Brazilian cohort and evaluate the prevalence of patients with a subacute progression of the disease. This was defined as the requirement of a wheelchair during the first 2 years after the onset of symptoms. Patients with this subacute course and patients with the chronic clinical course were compared in terms of their HTLV-I proviral loads (PLs) using real-time polymerase chain reaction (PCR). Seven out of 88 patients (7.9%) had a subacute progression. All patients were women and 5/7 acquired HTLV-I through sexual contact. There was no significant difference in the real-time PLs between the group with subacute evolution (mean 8.5 copies/100 cells, range 6.03 to 12.09) and those patients with a typical course of disease (mean 11.34 copies/100 cells, range 0.4 to 67.72) (P = .68), suggesting that factors other than the number of infected cells are implicated in the development of such an aggressive course of disease. Early recognition of this subgroup is important because immunosuppressive treatment might be beneficial if instituted promptly.
Insights
A rare subacute form of human T-lymphotropic virus type I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) affects 7.9% of patients. This aggressive HAM/TSP progression is not linked to higher HTLV-I proviral loads.
Area of Science:
- Neurology
- Infectious Diseases
- Virology
Background:
- Human T-lymphotropic virus type I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is typically a chronic neurological disorder.
- However, a rapid, subacute disease course has been observed in a subset of patients.
Purpose of the Study:
- To describe the clinical characteristics of HAM/TSP in a Brazilian cohort.
- To determine the prevalence of subacute HAM/TSP, defined by wheelchair dependency within 2 years of symptom onset.
- To compare HTLV-I proviral loads between patients with subacute and chronic HAM/TSP.
Main Methods:
- Retrospective analysis of a Brazilian cohort of HAM/TSP patients.
- Definition of subacute progression: wheelchair requirement within 2 years of symptom onset.
- Quantification of HTLV-I proviral loads using real-time polymerase chain reaction (PCR).
Main Results:
- Seven out of 88 patients (7.9%) exhibited a subacute HAM/TSP progression.
- All patients with subacute progression were female, with 5/7 acquiring HTLV-I sexually.
- No significant difference in HTLV-I proviral loads was found between the subacute and chronic HAM/TSP groups (P = .68).
Conclusions:
- A distinct subgroup of HAM/TSP patients experiences rapid disease progression, independent of HTLV-I proviral load.
- Early identification of subacute HAM/TSP is crucial for timely intervention.
- Prompt immunosuppressive treatment may offer benefits for patients with aggressive HAM/TSP.
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