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Supportive Oligonucleotide Therapy (SOT) as a Potential Treatment for Viral Infections and Lyme Disease: Preliminary Results

Authors :
Panagiotis Apostolou
Aggelos Iliopoulos
Georgios Beis
Ioannis Papasotiriou
Source :
Infectious Disease Reports, Vol 14, Iss 6, Pp 824-836 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Antisense therapy is widely used as an alternative therapeutic option for various diseases. RNA interference might be effective in infections, through the degradation of messenger RNA and, therefore, translation process. Hence, proteins essential for microorganisms and viruses’ proliferation and metabolism are inhibited, leading to their elimination. The present study aimed to evaluate the use of oligonucleotide in patients infected by Epstein–Barr (EBV) or Herpes Simplex Viruses 1/2 or with Lyme Disease caused by Borrelia burgdorferi. Blood samples were collected from 115 patients and the different species were characterized using molecular biology techniques. Then, SOT molecules (Supportive Oligonucleotide Therapy), which are specific small interfering RNA (siRNA), were designed, produced, and evaluated, for each specific strain. Oligonucleotides were administered intravenously to patients and then a quantitative Polymerase Chain Reaction was used to evaluate the effectiveness of SOT. This study revealed that for Lyme Disease, one or two SOT administrations can lead to a statistically significant decrease in DNA copies, while for viruses, two or three administrations are required to achieve a statistically significant reduction in the genetic material. These preliminary results indicate that antisense SOT therapy can be considered a potential treatment for viral as well as Lyme diseases.

Details

Language :
English
ISSN :
20367449
Volume :
14
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Infectious Disease Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.f2097bade52e41afa47f48ac0c2d3e42
Document Type :
article
Full Text :
https://doi.org/10.3390/idr14060084