Human T-lymphotropic virus type 1 and novel coronavirus disease 2019; More complex than just a simple coinfection

Gene. 2022 Aug 5:834:146550. doi: 10.1016/j.gene.2022.146550. Epub 2022 May 13.

Abstract

The recent coronavirus disease 2019 (COVID-19) significantly affected many people worldwide, especially those with underlying diseases. While some people with underlying illnesses, including cardiovascular diseases, are more vulnerable to develop severe COVID-19, other populations, including people who have autoimmune diseases, may develop severe diseases similar to the general population. The severity and outcome of COVID-19 are reviewed in individuals with underlying viral diseases, including acquired immune deficiency syndrome and hepatitis, however, some infectious diseases, including human T-lymphotropic virus type 1 (HTLV-1) diseases, is under-reported in the literature. HTLV-1 is a sexually transmitted disease that is endemic in some parts of the world. Infected patients may develop clinical symptoms of HTLV-1 associated myelopathy / tropical spastic paraparesis (HAM/TSP) and adult T cell leukemia (ATL) or may remain asymptomatic during their life. To the best of our knowledge, no clinical studies evaluate the severity and outcomes of SARS-CoV-2 infection in HTLV-1 infected patients. We aimed to review the pathogenesis of both of these viral infections and discuss their similarities in provoking immune responses. Although HTLV-1 infected patients may have had variable degrees of inflammation and immune system dysregulation, the available data is limited to conclude that HTLV-1 infected patients may be more vulnerable to developing severe COVID-19 in contrast to the general population.

Keywords: Adult T cell leukemia; Coronavirus disease 2019; Human T-lymphotropic virus type 1; Myelopathy – tropical spastic paraparesis.

Publication types

  • Review

MeSH terms

  • Adult
  • COVID-19*
  • Coinfection*
  • Human T-lymphotropic virus 1*
  • Humans
  • Paraparesis, Tropical Spastic* / diagnosis
  • SARS-CoV-2