Anna Paula Silva Olak
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Anna Paula Silva Olak has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Bruna Carolina Gonçalves
Laboratory of Basic and Applied Bacteriology, State University of Londrina, P.O. Box 10.011, Londrina 86057-970, Brazil
1 shared publication - Daniele Zendrini Rechenchoski
Departamento de Microbiologia, CCB, Universidade Estadual de Londrina, 86051–990, Londrina, PR, Brasil
1 shared publication Leticia Nishi
Departamento de Ciências Patológicas Centro de Ciências Biológicas Universidade Estadual de Londrina Londrina 86057‐970 Brazil
1 shared publication- Ligia Carla Faccin-Galhardi
Departamento de Microbiologia, CCB, Universidade Estadual de Londrina, Londrina, Paraná, CEP 86057-970, Brazil
1 shared publication - Maria Angelica Ehara Watanabe
Department of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, PR, 86057-970, Brazil.
1 shared publication - Mario Gabriel Lopes Barboza
Laboratório de Virologia Clínica e Molecular—LVCM, Departamento de Microbiologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo 05508-000, SP, Brazil
1 shared publication
Latest Publications
- 4 October 2020
- Published by Wiley in Fundamental & Clinical Pharmacology
- Vol. 35 (2) , 305-320
Antiviral therapies: advances and perspectives
Viral infections cause high morbidity and mortality, threaten public health, and impose a socioeconomic burden. We have seen the recent emergence of SARS‐CoV‐2 (Severe Acute Respiratory Syndrome Coronavirus 2), the causative agent of COVID‐19 that has already infected more than 29 million people, with more than 900 000 deaths since its identification in December 2019. Considering the significant impact of viral infections, research and development of new antivirals and control strategies are essential. In this paper, we summarize 96 antivirals approved by the Food and Drug Administration between 1987 and 2019. Of these, 49 (51%) are used in treatments against human immunodeficiency virus (HIV), four against human papillomavirus, six against cytomegalovirus, eight against hepatitis B virus, five against influenza, six against herpes simplex virus, 17 against hepatitis C virus and one against respiratory syncytial virus. This review also describes future perspectives for new antiviral therapies such as nanotechnologies, monoclonal antibodies and the CRISPR‐Cas system. These strategies are suggested as inhibitors of viral replication by various means, such as direct binding to the viral particle, blocking the infection, changes in intracellular mechanisms or viral genes, preventing replication and virion formation. We also observed that a large number of viral agents have no therapy available and the majority of those approved in the last 32 years are restricted to some groups, especially anti‐HIV. Additionally, the emergence of new viruses and strains resistant to available antivirals has necessitated the formulation of new antivirals.
- 4 October 2020
- Published by Wiley in Fundamental & Clinical Pharmacology
- Vol. 35 (2) , 305-320
Antiviral therapies: advances and perspectives
Viral infections cause high morbidity and mortality, threaten public health, and impose a socioeconomic burden. We have seen the recent emergence of SARS‐CoV‐2 (Severe Acute Respiratory Syndrome Coronavirus 2), the causative agent of COVID‐19 that has already infected more than 29 million people, with more than 900 000 deaths since its identification in December 2019. Considering the significant impact of viral infections, research and development of new antivirals and control strategies are essential. In this paper, we summarize 96 antivirals approved by the Food and Drug Administration between 1987 and 2019. Of these, 49 (51%) are used in treatments against human immunodeficiency virus (HIV), four against human papillomavirus, six against cytomegalovirus, eight against hepatitis B virus, five against influenza, six against herpes simplex virus, 17 against hepatitis C virus and one against respiratory syncytial virus. This review also describes future perspectives for new antiviral therapies such as nanotechnologies, monoclonal antibodies and the CRISPR‐Cas system. These strategies are suggested as inhibitors of viral replication by various means, such as direct binding to the viral particle, blocking the infection, changes in intracellular mechanisms or viral genes, preventing replication and virion formation. We also observed that a large number of viral agents have no therapy available and the majority of those approved in the last 32 years are restricted to some groups, especially anti‐HIV. Additionally, the emergence of new viruses and strains resistant to available antivirals has necessitated the formulation of new antivirals.