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IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis

HTLV-1 infections are persistent and frequently latent; however, productive infections trigger different types of immunological responses that utilize cytokines to control infection. The present study investigated the role of IFNG +874A/T polymorphisms among 153 HTLV-1-infected individuals (33 clini...

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Autores principales: Queiroz, Maria A. F., Azevedo, Vânia N., Amoras, Ednelza da S. G., Moura, Tuane C. F., Guimarães Ishak, Marluísa de O., Ishak, Ricardo, Vallinoto, Antonio C. R., Martins Feitosa, Rosimar N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968086/
https://www.ncbi.nlm.nih.gov/pubmed/29867783
http://dx.doi.org/10.3389/fmicb.2018.00795
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author Queiroz, Maria A. F.
Azevedo, Vânia N.
Amoras, Ednelza da S. G.
Moura, Tuane C. F.
Guimarães Ishak, Marluísa de O.
Ishak, Ricardo
Vallinoto, Antonio C. R.
Martins Feitosa, Rosimar N.
author_facet Queiroz, Maria A. F.
Azevedo, Vânia N.
Amoras, Ednelza da S. G.
Moura, Tuane C. F.
Guimarães Ishak, Marluísa de O.
Ishak, Ricardo
Vallinoto, Antonio C. R.
Martins Feitosa, Rosimar N.
author_sort Queiroz, Maria A. F.
collection PubMed
description HTLV-1 infections are persistent and frequently latent; however, productive infections trigger different types of immunological responses that utilize cytokines to control infection. The present study investigated the role of IFNG +874A/T polymorphisms among 153 HTLV-1-infected individuals (33 clinically diagnosed with TSP/HAM, 22 with rheumatologic manifestations, 2 with dermatitis, 1 with uveitis, and 95 asymptomatic patients) and 300 healthy control individuals. Genotyping and proviral HTLV-1 load assessment were performed using real-time PCR assays, and the plasma levels of IFN-γ were measured using an enzyme immunoassay (ELISA). Genotype frequencies were not significantly different, but the presence of the T allele was higher (p < 0.0142) among the asymptomatic patients. Plasma levels of IFN-γ were significantly higher (p < 0.0137) among those with the TT genotype. Their proviral load was also higher, although this elevation did not reach statistical significance. There was no difference in the IFN-γ plasma levels among the symptomatic patients, even when ranked according to disease severity (TSP/HAM or rheumatologic manifestations). However, the difference among asymptomatic patients with the T allele was significantly higher (p < 0.0016) and similar to the plasma levels observed among symptomatic individuals. These results suggest that the IFNG +874A/T polymorphism may modulate the plasma levels of IFN-γ during HTLV-1 infection. Asymptomatic carriers of the polymorphic genotypes appear to develop an inflammatory response in a shorter timeframe, triggering progression to HTLV-1-related symptoms and disorders. These results further suggest that HTLV-1-infected asymptomatic individuals expressing the IFNG +874A/T polymorphism should be monitored more closely in order to readily detect the increase in clinical symptoms, as these patients are potentially at risk of a poor prognosis and should therefore start available treatment procedures earlier.
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spelling pubmed-59680862018-06-04 IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis Queiroz, Maria A. F. Azevedo, Vânia N. Amoras, Ednelza da S. G. Moura, Tuane C. F. Guimarães Ishak, Marluísa de O. Ishak, Ricardo Vallinoto, Antonio C. R. Martins Feitosa, Rosimar N. Front Microbiol Microbiology HTLV-1 infections are persistent and frequently latent; however, productive infections trigger different types of immunological responses that utilize cytokines to control infection. The present study investigated the role of IFNG +874A/T polymorphisms among 153 HTLV-1-infected individuals (33 clinically diagnosed with TSP/HAM, 22 with rheumatologic manifestations, 2 with dermatitis, 1 with uveitis, and 95 asymptomatic patients) and 300 healthy control individuals. Genotyping and proviral HTLV-1 load assessment were performed using real-time PCR assays, and the plasma levels of IFN-γ were measured using an enzyme immunoassay (ELISA). Genotype frequencies were not significantly different, but the presence of the T allele was higher (p < 0.0142) among the asymptomatic patients. Plasma levels of IFN-γ were significantly higher (p < 0.0137) among those with the TT genotype. Their proviral load was also higher, although this elevation did not reach statistical significance. There was no difference in the IFN-γ plasma levels among the symptomatic patients, even when ranked according to disease severity (TSP/HAM or rheumatologic manifestations). However, the difference among asymptomatic patients with the T allele was significantly higher (p < 0.0016) and similar to the plasma levels observed among symptomatic individuals. These results suggest that the IFNG +874A/T polymorphism may modulate the plasma levels of IFN-γ during HTLV-1 infection. Asymptomatic carriers of the polymorphic genotypes appear to develop an inflammatory response in a shorter timeframe, triggering progression to HTLV-1-related symptoms and disorders. These results further suggest that HTLV-1-infected asymptomatic individuals expressing the IFNG +874A/T polymorphism should be monitored more closely in order to readily detect the increase in clinical symptoms, as these patients are potentially at risk of a poor prognosis and should therefore start available treatment procedures earlier. Frontiers Media S.A. 2018-05-18 /pmc/articles/PMC5968086/ /pubmed/29867783 http://dx.doi.org/10.3389/fmicb.2018.00795 Text en Copyright © 2018 Queiroz, Azevedo, Amoras, Moura, Guimarães Ishak, Ishak, Vallinoto and Martins Feitosa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Queiroz, Maria A. F.
Azevedo, Vânia N.
Amoras, Ednelza da S. G.
Moura, Tuane C. F.
Guimarães Ishak, Marluísa de O.
Ishak, Ricardo
Vallinoto, Antonio C. R.
Martins Feitosa, Rosimar N.
IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis
title IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis
title_full IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis
title_fullStr IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis
title_full_unstemmed IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis
title_short IFNG +874A/T Polymorphism Among Asymptomatic HTLV-1-Infected Individuals Is Potentially Related to a Worse Prognosis
title_sort ifng +874a/t polymorphism among asymptomatic htlv-1-infected individuals is potentially related to a worse prognosis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968086/
https://www.ncbi.nlm.nih.gov/pubmed/29867783
http://dx.doi.org/10.3389/fmicb.2018.00795
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