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Review
. 2007;21(1):9-15.
doi: 10.2165/00063030-200721010-00002.

Therapeutic and prophylactic potential of small interfering RNAs against severe acute respiratory syndrome: progress to date

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Review

Therapeutic and prophylactic potential of small interfering RNAs against severe acute respiratory syndrome: progress to date

Zhijie Chang et al. BioDrugs. 2007.

Abstract

Severe acute respiratory syndrome (SARS), caused by the novel coronavirus SARS-CoV, produced a scare when it appeared in 2003 in China and later quickly spread to other countries around the world. Although it has since disappeared, its threat to human health remains. Therefore, studies on the prevention and treatment of SARS are important for dealing with epidemics of this and other infectious diseases. The most promising newly developed technology for intervention in SARS may be RNA interference, an endogenous cellular process for the inhibition of gene expression mediated by sequence-specific double-stranded RNAs. Numerous studies have reported the therapeutic potential of RNA interference for the treatment of various human diseases ranging from cancers to infectious diseases such as HIV and hepatitis. To date, most studies on inhibition of SARS-CoV replication using small interfering RNAs (siRNAs) have been conducted in cell lines in vitro. One study using siRNAs to inhibit SARS-CoV infection in Rhesus macaques demonstrated that siRNAs were effective both prophylactically and therapeutically with no adverse effects in the animals. Challenges remaining for the application of siRNA in vivo for SARS prevention and treatment include the specificity of the siRNAs and the efficiency of delivery. However, with improvements in siRNA design and delivery methods, RNA interference has the potential to become another major weapon for combating dangerous infections due to viruses such as SARS-CoV.

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Table I
Table I
A summary of the small interfering RNAs designed to target sequences of the severe acute respiratory syndrome-associated coronavirus (SARS-CoV)

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References

    1. Parry J. SARS virus identified, but the disease is still spreading. BMJ. 2003;326(7395):897. doi: 10.1136/bmj.326.7395.897. - DOI - PMC - PubMed
    1. Skowronski D.M., Astell C., Brunham R.C., et al. Severe acute respiratory syndrome (SARS): a year in review. Annu Rev Med. 2005;56:357–81. doi: 10.1146/annurev.med.56.091103.134135. - DOI - PubMed
    1. Cinatl J, Jr, Michaelis M., Hoever G., et al. Development of antiviral therapy for severe acute respiratory syndrome. Antiviral Res. 2005;66(2–3):81–97. doi: 10.1016/j.antiviral.2005.03.002. - DOI - PMC - PubMed
    1. Holmes K.V. SARS-associated coronavirus. N Engl J Med. 2003;348(20):1948–51. doi: 10.1056/NEJMp030078. - DOI - PubMed
    1. Drosten C., Gunther S., Preiser W., et al. Identification of a novel coronavirus in patients with severe acute respiratory syndrome. N Engl J Med. 2003;348(20):1967–76. doi: 10.1056/NEJMoa030747. - DOI - PubMed

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