Plasmatic proinflammatory chemokines levels are tricky markers to monitoring HTLV-1 carriers

The human T‐cell leukemia virus type 1 (HTLV‐1) is present throughout the world and is associated with HTLV‐1‐associated myelopathy/tropical spastic paraparesis (HAM/TSP) and other inflammatory conditions. The pathogenesis of HAM/TSP involves a chronic inflammatory response in central nervous system...

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Published in:Journal of medical virology Vol. 88; no. 8; pp. 1438 - 1447
Main Authors: Chaves, Daniel Gonçalves, Sales, Camila Campos, de Cássia Gonçalves, Poliane, da Silva-Malta, Maria Clara Fernandes, Romanelli, Luiz Cláudio, Ribas, João Gabriel, de Freitas Carneiro-Proietti, Anna Bárbara, Martins, Marina Lobato
Format: Journal Article
Language:English
Published: United States Blackwell Publishing Ltd 01-08-2016
Wiley Subscription Services, Inc
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Summary:The human T‐cell leukemia virus type 1 (HTLV‐1) is present throughout the world and is associated with HTLV‐1‐associated myelopathy/tropical spastic paraparesis (HAM/TSP) and other inflammatory conditions. The pathogenesis of HAM/TSP involves a chronic inflammatory response in central nervous system (CNS), with the presence of HTLV‐1 infected cells and HTLV‐1‐specific CD8+ lymphocytes. Chemokines may have a role in the infiltration of these cells into the CNS. In this context, the present study analyzed the level of plasmatic chemokines CCL2 (MCP‐1), CCL5 (RANTES), IL8 (CXCL8), CXCL9 (MIG), and CXCL10 (IP‐10) and HTLV‐1 proviral load from peripheral blood in 162 asymptomatic carriers and 136 HAM/TSP patients to determine the differences that be associated with the clinical status of the HTLV‐1 infection. The results showed that patients with HAM/TSP have significantly higher levels of IL8 and CXCL9, and that the level of IL8, CXCL9 and CXCL10 was significantly greater in HTLV‐1 infected individuals with high (>1%) than those with low proviral load (<1%). However, the levels of the chemokines tested have not showed high sensitivity to discriminate HAM/TSP patients from asymptomatic carriers. In addition, chemokine profiles in asymptomatic carriers and HAM/TSP groups were similar, with no significant increased frequency of higher producers of chemokines in HAM/TSP individuals. Results indicate that the heterogeneity of the individuals in the groups regarding time of infection, duration of disease, proviral load level and other possible confound factors may impair the use of chemokines levels to monitor HTLV‐1 carriers in clinical practice. J. Med. Virol. 88:1438–1447, 2016. © 2016 Wiley Periodicals, Inc.
Bibliography:istex:F628EDBAA950C2ABB354FA3222A022056BA37F5F
ArticleID:JMV24481
CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico)
ark:/67375/WNG-1FWBQD57-F
Fundação Hemominas, FAPEMIG (Fundação de Amparo à Pesquisa do Estado de Minas Gerais)
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0146-6615
1096-9071
DOI:10.1002/jmv.24481