1. Neurologic, clinical, and immunologic features in a cohort of HTLV-1 carriers with high proviral loads
- Author
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Thiago Hebert, Mariele Guerra, Gabriela F. Costa, S. Ferraz, Edgar M. Carvalho, Cassius José Vitor de Oliveira, Lívia M. A. Oliveira, and José Abraão Carneiro Neto
- Subjects
Male ,0301 basic medicine ,Proviral load ,Myelopathy ,Gene Expression ,Gastroenterology ,Pathogenesis ,Erectile Dysfunction ,Proviruses ,immune system diseases ,Tropical spastic paraparesis ,HTLV-1 carriers ,Longitudinal Studies ,Prospective cohort study ,Human T-lymphotropic virus 1 ,Incidence (epidemiology) ,virus diseases ,Middle Aged ,Viral Load ,Interleukin-10 ,Sjogren's Syndrome ,Neurology ,Carrier State ,Cohort ,Female ,Nocturia ,Adult ,medicine.medical_specialty ,030106 microbiology ,Article ,Interferon-gamma ,03 medical and health sciences ,Cellular and Molecular Neuroscience ,Virology ,Sicca syndrome ,Internal medicine ,medicine ,Humans ,Risk factor ,Aged ,Tumor Necrosis Factor-alpha ,business.industry ,medicine.disease ,HTLV-I Infections ,030104 developmental biology ,HTLV-1 ,Leukocytes, Mononuclear ,Neurology (clinical) ,business ,HTLV-1-associated myelopathy - Abstract
A high proviral load (PVL) is recognized as a risk factor for human T cell leukemia virus-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP), but there is a lack of prospective studies evaluating whether or not HTLV-1 carriers with high PVL are at risk of developing HAM/TSP or other HTLV-1-related diseases. Here, we compare the incidence of clinical manifestations and the cytokine levels in 30 HTLV-1 carriers with high (> 50,000 copies/106 PBMC) and an equal number of subjects with low proviral load. Participants were followed for 3 to 16 years (median of 11 years). The PVL, IFN-γ, TNF, and IL-10 levels were quantified at entry and at the end of the follow-up. Among the self-reported symptoms in the initial evaluation, only the presence of paresthesia on the hands was more frequent in the group with high PVL (p p
- Published
- 2020