﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Advanced Pharmaceutical Bulletin</JournalTitle>
      <Issn>2228-5881</Issn>
      <Volume>8</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2018</Year>
        <Month>11</Month>
        <DAY>29</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>The Impact of CRISPR-Cas System on Antiviral Therapy</ArticleTitle>
    <FirstPage>591</FirstPage>
    <LastPage>597</LastPage>
    <ELocationID EIdType="doi">10.15171/apb.2018.067</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hadi</FirstName>
        <LastName>Bayat</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-4069-3529</Identifier>
      </Author>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Naderi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-4093-6041</Identifier>
      </Author>
      <Author>
        <FirstName>Amjad Hayat</FirstName>
        <LastName>Khan</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-3656-5727</Identifier>
      </Author>
      <Author>
        <FirstName>Arash</FirstName>
        <LastName>Memarnejadian</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-4005-8787</Identifier>
      </Author>
      <Author>
        <FirstName>Azam</FirstName>
        <LastName>Rahimpour</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-3296-5881</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/apb.2018.067</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>01</Month>
        <Day>17</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>09</Month>
        <Day>29</Day>
      </PubDate>
    </History>
    <Abstract>Clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein nuclease (Cas) is identified as an adaptive immune system in archaea and bacteria. Type II of this system, CRISPR-Cas9, is the most versatile form that has enabled facile and efficient targeted genome editing. Viral infections have serious impacts on global health and conventional antiviral therapies have not yielded a successful solution hitherto. The CRISPR-Cas9 system represents a promising tool for eliminating viral infections. In this review, we highlight 1) the recent progress of CRISPR-Cas technology in decoding and diagnosis of viral outbreaks, 2) its applications to eliminate viral infections in both pre-integration and provirus stages, and 3) various delivery systems that are employed to introduce the platform into target cells. </Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">CRISPR-Cas</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Antiviral therapy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Genome editing</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Latent viruses</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Delivery system</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>