Self-complementary adeno-associated virus (scAAV)

From Wikipedia, the free encyclopedia
Jump to: navigation, search
self-complementary
adeno-associated virus
Virus classification
Group: Group II (ssDNA)
Family: Parvoviridae
Subfamily: Parvovirinae
Genus: Dependovirus
Species: self-complementary adeno-associated virus

Self-complementary adeno-associated virus (scAAV) is a viral vector engineered from the naturally occurring adeno-associated virus (AAV) to be used as a tool for gene therapy.[1] Use of recombinant AAV (rAAV) has been successful in clinical trials addressing a variety of diseases.[2] This lab-made progeny of rAAV is termed "self-complementary" because the coding region has been designed to form an intra-molecular double-stranded DNA template. A rate-limiting step for the standard AAV genome involves the second-strand synthesis since the typical AAV genome is a single-stranded DNA template.[3][4] However, this is not the case for scAAV genomes. Upon infection, rather than waiting for cell mediated synthesis of the second strand, the two complementary halves of scAAV will associate to form one double stranded DNA (dsDNA) unit that is ready for immediate replication and transcription. The caveat of this construct is that instead of the full coding capacity found in rAAV (4.7-6kb)[5] scAAV can only hold about half of that amount (≈2.4kb).[6]

In gene therapy application utilizing rAAV, the virus transduces the cell with a single stranded DNA (ssDNA) flanked by two Inverted Terminal Repeats (ITRs). These ITRs form hairpins at the end of the sequence to serve as primers to initiate synthesis of the second strand before subsequent steps of infection can begin. The second strand synthesis is considered to be one of several blocks to efficient infection.[7] Additional advantages of scAAV include increased and prolonged transgene expression in vitro and in vivo, as well as "higher in vivo DNA stability and more effective circularization."[8]

scAAV in Gene Therapy[edit]

scAAV is an attractive vector for use in gene therapy for many reasons. Its parent vector, AAV, is already being used in clinical trials.[9] Due to a variety of scAAV serotypes available, scientists can choose a serotype which has properties desirable for their therapy. Selecting only a subset of cells improves specificity and lowers the risk of being inhibited by the immune system. Different scAAV and AAV serotypes can efficiently transfect a variety of cellular targets.[10][11] Like all vector-based approaches to gene therapy, one obstacle in translating therapies from pre-clinical trials into a human clinical application will be the production of large quantities of highly concentrated virus [12] One disadvantage that scAAV faces is that due to robust gene expression, transgene products delivered via scAAV elicit a stronger immune response than those same transgenes delivered via a single-stranded AAV vector.[13]

Virus Classification[edit]

Like AAV, scAAV is a member of the family Parvoviridae, commonly known as parvoviruses. These viruses are nonenveloped, single-strand DNA (ssDNA) viruses. Within Parvoviridae, scAAV further belongs to the Dependovirus genus, characteristically defined by an inability to replicate on their own. In nature, these viruses depend on another virus to provide replication machinery; adeno-associated virus can only replicate during an active infection of adenovirus or some types of herpesvirus. In lab use, this obstacle is overcome by addition of the helper plasmids, which exogenously expresses replication genes which AAV itself lacks.[14]

Viral Replication[edit]

As a dependovirus, scAAV remains in a latent state within the cell until the cell experiences certain permissive conditions. These can include presence of a helper virus infection (such as adenovirus) or other toxic events such as exposure to UV light or carcinogens.[14] Because the endogenous rep ORF has been replaced with transgene, exogenously provided rep genes encode the proteins required for genome replication and other viral life cycle components. The ITRs located 5' and 3' of the viral genome serve as the origin of replication.[15]

Viral Packaging[edit]

Like the rep ORF, scAAV's cap ORF has been replaced by transgene and therefore is provided exogenously in a lab environment. The genes encoded in this ORF build capsid proteins and are responsible (along with intracellular processing) for conveying target specificity. Rep proteins participate in the integration of the genome into preformed capsids.[15] Despite the fact that scAAV is designed to form dsDNA upon infection, the two complementary strands are not packaged in a double stranded manner. Parvoviruses package their viral genome such that the ssDNA bases come in contact with the amino acids on the inside of the viral capsid. Thus the sequence of scAAV is likely unwound by a virally encoded DNA helicase before being packaged into viral protein capsid.[7]

References[edit]

  1. ^ McCarty, D M; Monahan, P E; Samulski, R J (2001). "Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis". Gene Therapy 8 (16): 1248–54. doi:10.1038/sj.gt.3301514. PMID 11509958. 
  2. ^ http://www.wiley.com//legacy/wileychi/genmed/clinical/
  3. ^ Ferrari, FK; Samulski, T; Shenk, T; Samulski, RJ (1996). "Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors". Journal of Virology 70 (5): 3227–34. PMC 190186. PMID 8627803. 
  4. ^ Fisher, KJ; Gao, GP; Weitzman, MD; Dematteo, R; Burda, JF; Wilson, JM (1996). "Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis". Journal of Virology 70 (1): 520–32. PMC 189840. PMID 8523565. 
  5. ^ Grieger, J. C.; Samulski, R. J. (2005). "Packaging Capacity of Adeno-Associated Virus Serotypes: Impact of Larger Genomes on Infectivity and Postentry Steps". Journal of Virology 79 (15): 9933–44. doi:10.1128/JVI.79.15.9933-9944.2005. PMC 1181570. PMID 16014954. 
  6. ^ Wu, J; Zhao, W; Zhong, L; Han, Z; Li, B; Ms, W; Weigel-Kelley, KA; Warrington, KH; Srivastava, A (Feb 2007). "Self-complementary recombinant adeno-associated viral vectors: packaging capacity and the role of rep proteins in vector purity". Hum Gene Therapy 18 (2): 171–82. doi:10.1089/hum.2006.088. PMID 17328683. 
  7. ^ a b McCarty, Douglas M (2008). "Self-complementary AAV Vectors; Advances and Applications". Molecular Therapy 16 (10): 1648–56. doi:10.1038/mt.2008.171. PMID 18682697. 
  8. ^ Wang, Z; Ma, H-I; Li, J; Sun, L; Zhang, J; Xiao, X (2003). "Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo". Gene Therapy 10 (26): 2105–11. doi:10.1038/sj.gt.3302133. PMID 14625564. 
  9. ^ Aalbers, Caroline J.; Tak, Paul P.; Vervoordeldonk, Margriet J. (2011). "Advancements in adeno-associated viral gene therapy approaches: Exploring a new horizon". F1000 Medicine Reports 3. doi:10.3410/M3-17. 
  10. ^ Hillestad ML, Guenzel AJ, Nath KA, Barry MA. A vector-host system to fingerprint virus tropism. Hum Gene Ther. 2012 Oct;23(10):1116-26. doi:10.1089/hum.2011.116. PubMed PMID 22834781; PubMed Central PMCID: PMC3472556.
  11. ^ Zincarelli C, Soltys S, Rengo G, Rabinowitz JE. Analysis of AAV serotypes 1-9 mediated gene expression and tropism in mice after systemic injection. Mol Ther. 2008 Jun;16(6):1073-80. doi:10.1038/mt.2008.76. Epub 2008 Apr 15. PubMed PMID 18414476.
  12. ^ Clément N, Knop DR, Byrne BJ. Large-scale adeno-associated viral vector production using a herpesvirus-based system enables manufacturing for clinical studies. Hum Gene Ther. 2009 Aug;20(8):796-806. doi:10.1089/hum.2009.094. Review. PubMed PMID 19569968; PubMed Central PMCID: PMC2861951
  13. ^ Wu T, Töpfer K, Lin SW, Li H, Bian A, Zhou XY, High KA, Ertl HC. Self-complementary AAVs induce more potent transgene product-specific immune responses compared to a single-stranded genome. Mol Ther. 2012 Mar;20(3):572-9. doi:10.1038/mt.2011.280. Epub 2011 Dec 20. PubMed PMID 22186792; PubMed Central PMCID: PMC3293612.
  14. ^ a b Berns KI. Parvovirus replication. Microbiol Rev. 1990 Sep;54(3):316-29. Review. PubMed PMID 2215424; PubMed Central PMCID: PMC372780.
  15. ^ a b Büning H, Perabo L, Coutelle O, Quadt-Humme S, Hallek M. Recent developments in adeno-associated virus vector technology. J Gene Med. 2008 Jul;10(7):717-33. doi:10.1002/jgm.1205. Review. PubMed PMID 18452237.