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Adeno-associated Virus Vectors Efficiently Transduce Mouse and Rabbit Sensory Neurons Coinfected with Herpes Simplex Virus 1 following Peripheral Inoculation.

Watson ZL, Ertel MK, Lewin AS, Tuli SS, Schultz GS, Neumann DM, Bloom DC. Watson ZL, et al. J Virol. 2016 Aug 12;90(17):7894-901. doi: 10.1128/JVI.01028-16. Print 2016 Sep 1. J Virol. 2016. PMID: 27334582 Free PMC article.

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Tyrosine Mutation in AAV9 Capsid Improves Gene Transfer to the Mouse Lung.

Martini SV, Silva AL, Ferreira D, Rabelo R, Ornellas FM, Gomes K, Rocco PR, Petrs-Silva H, Morales MM. Martini SV, et al. Cell Physiol Biochem. 2016;39(2):544-53. doi: 10.1159/000445646. Epub 2016 Jul 7. Cell Physiol Biochem. 2016. PMID: 27384068 Free article.

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Targeting T cell malignancies using CAR-based immunotherapy: challenges and potential solutions.

Fleischer LC, Spencer HT, Raikar SS. Fleischer LC, et al. J Hematol Oncol. 2019 Dec 29;12(1):141. doi: 10.1186/s13045-019-0801-y. J Hematol Oncol. 2019. PMID: 31884955 Free PMC article. Review.

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Serotype survey of AAV gene delivery via subconjunctival injection in mice.

Song L, Llanga T, Conatser LM, Zaric V, Gilger BC, Hirsch ML. Song L, et al. Gene Ther. 2018 Sep;25(6):402-414. doi: 10.1038/s41434-018-0035-6. Epub 2018 Aug 2. Gene Ther. 2018. PMID: 30072815

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Optimizing the transduction efficiency of capsid-modified AAV6 serotype vectors in primary human hematopoietic stem cells in vitro and in a xenograft mouse model in vivo.

Song L, Kauss MA, Kopin E, Chandra M, Ul-Hasan T, Miller E, Jayandharan GR, Rivers AE, Aslanidi GV, Ling C, Li B, Ma W, Li X, Andino LM, Zhong L, Tarantal AF, Yoder MC, Wong KK Jr, Tan M, Chatterjee S, Srivastava A. Song L, et al. Cytotherapy. 2013 Aug;15(8):986-98. doi: 10.1016/j.jcyt.2013.04.003. Cytotherapy. 2013. PMID: 23830234 Free PMC article.

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Efficient modification of CCR5 in primary human hematopoietic cells using a megaTAL nuclease and AAV donor template.

Sather BD, Romano Ibarra GS, Sommer K, Curinga G, Hale M, Khan IF, Singh S, Song Y, Gwiazda K, Sahni J, Jarjour J, Astrakhan A, Wagner TA, Scharenberg AM, Rawlings DJ. Sather BD, et al. Sci Transl Med. 2015 Sep 30;7(307):307ra156. doi: 10.1126/scitranslmed.aac5530. Sci Transl Med. 2015. PMID: 26424571 Free PMC article.

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Gene-edited pseudogene resurrection corrects p47^phox-deficient chronic granulomatous disease.

Merling RK, Kuhns DB, Sweeney CL, Wu X, Burkett S, Chu J, Lee J, Koontz S, Di Pasquale G, Afione SA, Chiorini JA, Kang EM, Choi U, De Ravin SS, Malech HL. Merling RK, et al. Blood Adv. 2016 Dec 28;1(4):270-278. doi: 10.1182/bloodadvances.2016001214. eCollection 2017 Jan 10. Blood Adv. 2016. PMID: 29296942 Free PMC article.

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Optimization of AAV6 transduction enhances site-specific genome editing of primary human lymphocytes.

Rogers GL, Huang C, Clark RDE, Seclén E, Chen HY, Cannon PM. Rogers GL, et al. Mol Ther Methods Clin Dev. 2021 Sep 10;23:198-209. doi: 10.1016/j.omtm.2021.09.003. eCollection 2021 Dec 10. Mol Ther Methods Clin Dev. 2021. PMID: 34703842 Free PMC article.

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AAV Vectors: Are They Safe?

Srivastava A. Srivastava A. Hum Gene Ther. 2020 Jul;31(13-14):697-699. doi: 10.1089/hum.2020.187. Hum Gene Ther. 2020. PMID: 32611206 No abstract available.

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Advances in the gene therapy of monogenic blood cell diseases.

Bueren JA, Quintana-Bustamante O, Almarza E, Navarro S, Río P, Segovia JC, Guenechea G. Bueren JA, et al. Clin Genet. 2020 Jan;97(1):89-102. doi: 10.1111/cge.13593. Epub 2019 Jul 11. Clin Genet. 2020. PMID: 31231794 Review.

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