Relevance of HTLV-1 proviral load in asymptomatic and symptomatic patients living in endemic and non-endemic areas of Argentina

PLoS One. 2019 Nov 22;14(11):e0225596. doi: 10.1371/journal.pone.0225596. eCollection 2019.

Abstract

HTLV-1 proviral load (pVL) in peripheral blood mononuclear cell (PBMCs) is proposed as a marker of disease progression but its role still remains controversial. The aim of this study was to evaluate the levels of HTLV-1 pVL in symptomatic patients and asymptomatic HTLV-1 carriers. In this cross-sectional study the pVL was measured by Real Time PCR in 102 asymptomatic carriers and 22 symptomatic patients (5ATLL, 15 TSP and 2 uveitis). We observed that the HTLV-1 pVL was significantly higher in symptomatic patients (median = 4.99 log10 HTLV-1 copies /106 PBMCs) compared to asymptomatic HTLV-1 carriers (median = 4.38 log10 HTLV-1 copies /106 PBMCs; p = 0.0030). A wide variation on the HTLV-1 pVL levels among asymptomatic HTLV-1 carriers was observed with some pVL as high as those observed in symptomatic patients. The asymptomatic HTLV-1 carriers were divided according to the place of birth and the highest levels of pVL were detected among patients from endemics areas from the North of Argentina. Our results reinforce the usefulness of the proviral load would be a prognostic marker of HTLV-1 disease progression. Moreover, host, viral or socio-environmental factors cannot be excluded as determinant of high proviral load.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Argentina / epidemiology
  • Cross-Sectional Studies
  • Endemic Diseases
  • Female
  • HTLV-I Infections / epidemiology
  • HTLV-I Infections / pathology*
  • Human T-lymphotropic virus 1 / genetics
  • Human T-lymphotropic virus 1 / isolation & purification
  • Human T-lymphotropic virus 1 / physiology*
  • Humans
  • Leukocytes, Mononuclear / virology
  • Male
  • Middle Aged
  • RNA, Viral / metabolism
  • Real-Time Polymerase Chain Reaction
  • Viral Load*

Substances

  • RNA, Viral

Grants and funding

This work was supported by Fondo Nacional para Ciencia y Tecnología (FONCYT) [grant number PICT 2010-0502], http://www.agencia.mincyt.gob.ar/foncyt.php. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.