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Adeno-associated virus vectors and neurotoxicity—lessons from preclinical and human studies

Abstract

Over 15 years after hepatotoxicity was first observed following administration of an adeno-associated virus (AAV) vector during a hemophilia B clinical trial, recent reports of treatment-associated neurotoxicity in animals and humans have brought the potential impact of AAV-associated toxicity back to prominence. In both pre-clinical studies and clinical trials, systemic AAV administration has been associated with neurotoxicity in peripheral nerve ganglia and spinal cord. Neurological signs have also been seen following direct AAV injection into the brain, both in non-human primates and in a clinical trial for late infantile Batten disease. Neurotoxic events appear variable across species, and preclinical animal studies do not fully predict clinical observations. Accumulating data suggest that AAV-associated neurotoxicity may be underdiagnosed and may differ between species in terms of frequency and/or severity. In this review, we discuss the different animal models that have been used to demonstrate AAV-associated neurotoxicity, its potential causes and consequences, and potential approaches to blunt AAV-associated neurotoxicity.

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Fig. 1: AAV delivery routes into the nervous system.

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No datasets were generated for this review. All works reviewed in this study are referenced in the published article.

References

  1. Colon-Thillet R, Jerome KR, Stone D. Optimization of AAV vectors to target persistent viral reservoirs. Virol J. 2021;18:85.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Wang D, Tai PWL, Gao G. Adeno-associated virus vector as a platform for gene therapy delivery. Nat Rev Drug Discov. 2019;18:358–78.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Hudry E, Vandenberghe LH. Therapeutic AAV gene transfer to the nervous system: a clinical reality. Neuron. 2019;101:839–62.

    Article  CAS  PubMed  Google Scholar 

  4. Morris JA, Boshoff CH, Schor NF, Wong LM, Gao G, Davidson BL. Next-generation strategies for gene-targeted therapies of central nervous system disorders: a workshop summary. Mol Ther. 2021;29:3332–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Schuster DJ, Dykstra JA, Riedl MS, Kitto KF, Belur LR, McIvor RS, et al. Biodistribution of adeno-associated virus serotype 9 (AAV9) vector after intrathecal and intravenous delivery in mouse. Front Neuroanat. 2014;8:42.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Hinderer C, Katz N, Buza EL, Dyer C, Goode T, Bell P, et al. Severe toxicity in nonhuman primates and piglets following high-dose intravenous administration of an adeno-associated virus vector expressing human SMN. Hum Gene Ther. 2018;29:285–98.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Hordeaux J, Buza EL, Dyer C, Goode T, Mitchell TW, Richman L, et al. Adeno-associated virus-induced dorsal root ganglion pathology. Hum Gene Ther. 2020;31:808–18.

    Article  CAS  PubMed  Google Scholar 

  8. Hordeaux J, Buza EL, Jeffrey B, Song C, Jahan T, Yuan Y, et al. MicroRNA-mediated inhibition of transgene expression reduces dorsal root ganglion toxicity by AAV vectors in primates. Sci Transl Med. 2020;12:eaba9188.

    Article  CAS  PubMed  Google Scholar 

  9. Hordeaux J, Hinderer C, Buza EL, Louboutin JP, Jahan T, Bell P, et al. Safe and sustained expression of human iduronidase after intrathecal administration of adeno-associated virus serotype 9 in infant Rhesus monkeys. Hum Gene Ther. 2019;30:957–66.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Hordeaux J, Hinderer C, Goode T, Buza EL, Bell P, Calcedo R, et al. Toxicology study of intra-cisterna magna adeno-associated virus 9 expressing iduronate-2-sulfatase in Rhesus macaques. Mol Ther Methods Clin Dev. 2018;10:68–78.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Hordeaux J, Hinderer C, Goode T, Katz N, Buza EL, Bell P, et al. Toxicology study of intra-cisterna magna adeno-associated virus 9 expressing human alpha-L-iduronidase in Rhesus macaques. Mol Ther Methods Clin Dev. 2018;10:79–88.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Hordeaux J, Wang Q, Katz N, Buza EL, Bell P, Wilson JM. The neurotropic properties of AAV-PHP.B are limited to C57BL/6J mice. Mol Ther. 2018;26:664–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Bolt MW, Brady JT, Whiteley LO, Khan KN. Development challenges associated with rAAV-based gene therapies. J Toxicol Sci. 2021;46:57–68.

    Article  CAS  PubMed  Google Scholar 

  14. EMA. Zolgensma assessment report. https://www.ema.europa.eu/en/documents/assessment-report/zolgensma-epar-public-assessment-report_en.pdf, 2020.

  15. Palazzi X, Pardo ID, Sirivelu MP, Newman L, Kumpf SW, Qian J, et al. Biodistribution and tolerability of AAV-PHP.B-CBh-SMN1 in wistar han rats and cynomolgus macaques reveal different toxicologic profiles. Hum Gene Ther. 2022;33:175–87.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Hinderer C, Bell P, Louboutin JP, Katz N, Zhu Y, Lin G, et al. Neonatal tolerance induction enables accurate evaluation of gene therapy for MPS I in a canine model. Mol Genet Metab. 2016;119:124–30.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Marco S, Haurigot V, Jaen ML, Ribera A, Sanchez V, Molas M, et al. Seven-year follow-up of durability and safety of AAV CNS gene therapy for a lysosomal storage disorder in a large animal. Mol Ther Methods Clin Dev. 2021;23:370–89.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Hordeaux J, Jeffrey BA, Jian J, Choudhury GR, Michalson K, Mitchell TW, et al. Efficacy and safety of a krabbe disease gene therapy. Hum Gene Ther. 2022.

  19. Buss N, Lanigan L, Zeller J, Cissell D, Metea M, Adams E, et al. Characterization of AAV-mediated dorsal root ganglionopathy. Mol Ther Methods Clin Dev. 2022;24:342–54.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Fader KA, Pardo ID, Kovi RC, Somps CJ, Wang HH, Vaidya VS, et al. Circulating neurofilament light chain as a promising biomarker of AAV-induced dorsal root ganglia toxicity in nonclinical toxicology species. Mol Ther Methods Clin Dev. 2022;25:264–77.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Johnston S, Parylak SL, Kim S, Mac N, Lim C, Gallina I, et al. AAV ablates neurogenesis in the adult murine hippocampus. Elife. 2021;10:e59291.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Ciesielska A, Hadaczek P, Mittermeyer G, Zhou S, Wright JF, Bankiewicz KS, et al. Cerebral infusion of AAV9 vector-encoding non-self proteins can elicit cell-mediated immune responses. Mol Ther. 2013;21:158–66.

    Article  CAS  PubMed  Google Scholar 

  23. Klein RL, Dayton RD, Leidenheimer NJ, Jansen K, Golde TE, Zweig RM. Efficient neuronal gene transfer with AAV8 leads to neurotoxic levels of tau or green fluorescent proteins. Mol Ther. 2006;13:517–27.

    Article  CAS  PubMed  Google Scholar 

  24. Samaranch L, Sebastian WS, Kells AP, Salegio EA, Heller G, Bringas JR, et al. AAV9-mediated expression of a non-self protein in nonhuman primate central nervous system triggers widespread neuroinflammation driven by antigen-presenting cell transduction. Mol Ther. 2014;22:329–37.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Zerah M, Piguet F, Colle MA, Raoul S, Deschamps JY, Deniaud J, et al. Intracerebral gene therapy using AAVrh.10-hARSA recombinant vector to treat patients with early-onset forms of metachromatic leukodystrophy: preclinical feasibility and safety assessments in nonhuman primates. Hum Gene Ther Clin Dev. 2015;26:113–24.

    Article  CAS  PubMed  Google Scholar 

  26. Crystal R. Clinical and nonclinical consequences of direct CNS parenchymal administration of AAV vectors: https://www.fda.gov/media/151998/download, 2021.

  27. Rosenberg JB, Chen A, De BP, Dyke JP, Ballon DJ, Monette S, et al. Safety of direct intraparenchymal AAVrh.10-mediated central nervous system gene therapy for metachromatic leukodystrophy. Hum Gene Ther. 2021;32:563–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Golebiowski D, van der Bom IMJ, Kwon CS, Miller AD, Petrosky K, Bradbury AM, et al. Direct intracranial injection of AAVrh8 encoding monkey beta-N-acetylhexosaminidase causes neurotoxicity in the primate brain. Hum Gene Ther. 2017;28:510–22.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Keiser MS, Ranum PT, Yrigollen CM, Carrell EM, Smith GR, Muehlmatt AL, et al. Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain. Nat Med. 2021;27:1982–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Davidson MK, Lindsey JR, Davis JK. Requirements and selection of an animal model. Isr J Med Sci. 1987;23:551–5.

    CAS  PubMed  Google Scholar 

  31. Eaton SL, Wishart TM. Bridging the gap: large animal models in neurodegenerative research. Mamm Genome. 2017;28:324–37.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Manno CS, Pierce GF, Arruda VR, Glader B, Ragni M, Rasko JJ, et al. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response. Nat Med. 2006;12:342–7.

    Article  CAS  PubMed  Google Scholar 

  33. Kuzmin DA, Shutova MV, Johnston NR, Smith OP, Fedorin VV, Kukushkin YS, et al. The clinical landscape for AAV gene therapies. Nat Rev Drug Discov. 2021;20:173–4.

    Article  CAS  PubMed  Google Scholar 

  34. Chand DH, Zaidman C, Arya K, Millner R, Farrar MA, Mackie FE, et al. Thrombotic microangiopathy following onasemnogene abeparvovec for spinal muscular atrophy: a case series. J Pediatr. 2021;231:265–8.

    Article  CAS  PubMed  Google Scholar 

  35. Feldman AG, Parsons JA, Dutmer CM, Veerapandiyan A, Hafberg E, Maloney N, et al. Subacute liver failure following gene replacement therapy for spinal muscular atrophy type 1. J Pediatr. 2020;225:252–8 e1.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. High-dose AAV gene therapy deaths. Nat Biotechnol. 2020; 38:910. https://doi.org/10.1038/s41587-020-0642-9

  37. Morales L, Gambhir Y, Bennett J, Stedman HH. Broader implications of progressive liver dysfunction and lethal sepsis in two boys following systemic high-dose AAV. Mol Ther. 2020;28:1753–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Astellas. Astellas reports update to September 1 announcement on the ASPIRO clinical trial of AT132 in patients with X-linked myotubular myopathy. https://newsroom.astellas.us/2021-09-14-Astellas-Reports-Update-to-September-1-Announcement-on-the-ASPIRO-Clinical-Trial-of-AT132-in-Patients-with-X-linked-Myotubular-Myopathy.

  39. Bonnemann C. AAV Related immunological safety and toxicity: preliminary clinical observations in the GAN and MTM1 trials. In Proceedings of virtual workshop on systemic immunogenicity considerations of AAV-mediated gene therapy, NIH, NCATS: https://videocast.nih.gov/watch=3854, 2020.

  40. Mueller C, Berry JD, McKenna-Yasek DM, Gernoux G, Owegi MA, Pothier LM, et al. SOD1 suppression with adeno-associated virus and MicroRNA in familial ALS. N Engl J Med. 2020;383:151–8.

    Article  CAS  PubMed  Google Scholar 

  41. Mullard A. Gene therapy community grapples with toxicity issues, as pipeline matures. Nat Rev Drug Discov. 2021;20:804–5.

    Article  CAS  PubMed  Google Scholar 

  42. Sondhi D, Kaminsky SM, Hackett NR, Pagovich OE, Rosenberg JB, De BP, et al. Slowing late infantile Batten disease by direct brain parenchymal administration of a rh.10 adeno-associated virus expressing CLN2. Sci Transl Med. 2020;12:eabb5413.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Reinhold AK, Rittner HL. Barrier function in the peripheral and central nervous system-a review. Pflugers Arch. 2017;469:123–34.

    Article  CAS  PubMed  Google Scholar 

  44. Weerasuriya A, Mizisin AP. The blood-nerve barrier: structure and functional significance. Methods Mol Biol. 2011;686:149–73.

    Article  CAS  PubMed  Google Scholar 

  45. Montague-Cardoso K, Malcangio M. Changes in blood-spinal cord barrier permeability and neuroimmune interactions in the underlying mechanisms of chronic pain. Pain Rep. 2021;6:e879.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Liu D, Zhu M, Zhang Y, Diao Y. Crossing the blood-brain barrier with AAV vectors. Metab Brain Dis. 2021;36:45–52.

    Article  PubMed  Google Scholar 

  47. Penaud-Budloo M, Francois A, Clement N, Ayuso E. Pharmacology of recombinant adeno-associated virus production. Mol Ther Methods Clin Dev. 2018;8:166–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Rumachik NG, Malaker SA, Poweleit N, Maynard LH, Adams CM, Leib RD, et al. Methods matter: standard production platforms for recombinant AAV produce chemically and functionally distinct vectors. Mol Ther Methods Clin Dev. 2020;18:98–118.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Robert MA, Chahal PS, Audy A, Kamen A, Gilbert R, Gaillet B. Manufacturing of recombinant adeno-associated viruses using mammalian expression platforms. Biotechnol J. 2017;12:1600193.

  50. Kondratova L, Kondratov O, Ragheb R, Zolotukhin S. Removal of endotoxin from rAAV samples using a simple detergent-based protocol. Mol Ther Methods Clin Dev. 2019;15:112–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Schnodt M, Buning H. Improving the quality of adeno-associated viral vector preparations: the challenge of product-related impurities. Hum Gene Ther Methods. 2017;28:101–8.

    Article  PubMed  Google Scholar 

  52. Wright JF. Codon modification and PAMPs in clinical AAV vectors: the tortoise or the hare? Mol Ther. 2020;28:701–3.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  53. Bevan AK, Duque S, Foust KD, Morales PR, Braun L, Schmelzer L, et al. Systemic gene delivery in large species for targeting spinal cord, brain, and peripheral tissues for pediatric disorders. Mol Ther. 2011;19:1971–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Foust KD, Nurre E, Montgomery CL, Hernandez A, Chan CM, Kaspar BK. Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes. Nat Biotechnol. 2009;27:59–65.

    Article  CAS  PubMed  Google Scholar 

  55. Pattali R, Mou Y, Li XJ. AAV9 Vector: a Novel modality in gene therapy for spinal muscular atrophy. Gene Ther. 2019;26:287–95.

    Article  CAS  PubMed  Google Scholar 

  56. Lykken EA, Shyng C, Edwards RJ, Rozenberg A, Gray SJ. Recent progress and considerations for AAV gene therapies targeting the central nervous system. J Neurodev Disord. 2018;10:16.

    Article  PubMed  PubMed Central  Google Scholar 

  57. Adachi K, Enoki T, Kawano Y, Veraz M, Nakai H. Drawing a high-resolution functional map of adeno-associated virus capsid by massively parallel sequencing. Nat Commun. 2014;5:3075.

    Article  PubMed  Google Scholar 

  58. Earley LF, Conatser LM, Lue VM, Dobbins AL, Li C, Hirsch ML, et al. Adeno-associated virus serotype-specific inverted terminal repeat sequence role in vector transgene expression. Hum Gene Ther. 2020;31:151–62.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Pan X, Yue Y, Boftsi M, Wasala LP, Tran NT, Zhang K, et al. Rational engineering of a functional CpG-free ITR for AAV gene therapy. Gene Ther. 2022;29:333–45.

  60. Ansari AM, Ahmed AK, Matsangos AE, Lay F, Born LJ, Marti G, et al. Cellular GFP toxicity and immunogenicity: potential confounders in in vivo cell tracking experiments. Stem Cell Rev Rep. 2016;12:553–9.

    Article  CAS  PubMed  Google Scholar 

  61. Hagedorn C, Schnodt-Fuchs M, Boehme P, Abdelrazik H, Lipps HJ, Buning H. S/MAR element facilitates episomal long-term persistence of adeno-associated virus vector genomes in proliferating cells. Hum Gene Ther. 2017;28:1169–79.

    Article  CAS  PubMed  Google Scholar 

  62. Powell SK, Rivera-Soto R, Gray SJ. Viral expression cassette elements to enhance transgene target specificity and expression in gene therapy. Discov Med. 2015;19:49–57.

    PubMed  PubMed Central  Google Scholar 

  63. Sun X, Yu X, Zhang L, Zhao W, Wang M, Zhang Y, et al. Comparison of the expression and toxicity of AAV2/9 carrying the human A53T alpha-synuclein gene in presence or absence of WPRE. Heliyon. 2021;7:e06302.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Favre D, Blouin V, Provost N, Spisek R, Porrot F, Bohl D, et al. Lack of an immune response against the tetracycline-dependent transactivator correlates with long-term doxycycline-regulated transgene expression in nonhuman primates after intramuscular injection of recombinant adeno-associated virus. J Virol. 2002;76:11605–11.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Ertl HCJ. T cell-mediated immune responses to AAV and AAV vectors. Front Immunol. 2021;12:666666.

    Article  PubMed  PubMed Central  Google Scholar 

  66. Herzog RW. Complexity of immune responses to AAV transgene products—example of factor IX. Cell Immunol. 2019;342:103658.

    Article  PubMed  Google Scholar 

  67. Muhuri M, Maeda Y, Ma H, Ram S, Fitzgerald KA, Tai PW, et al. Overcoming innate immune barriers that impede AAV gene therapy vectors. J Clin Investig. 2021;131:e143780.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Nathwani AC, Tuddenham EG, Rangarajan S, Rosales C, McIntosh J, Linch DC, et al. Adenovirus-associated virus vector-mediated gene transfer in hemophilia B. N Engl J Med. 2011;365:2357–65.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  69. Perez BA, Shutterly A, Chan YK, Byrne BJ, Corti M. Management of neuroinflammatory responses to AAV-mediated gene therapies for neurodegenerative diseases. Brain Sci. 2020;10:119.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  70. Suriano CM, Verpeut JL, Kumar N, Ma J, Jung C, Boulanger LM. Adeno-associated virus (AAV) reduces cortical dendritic complexity in a TLR9-dependent manner. bioRxiv.org 2021. https://doi.org/10.1101/2021.09.28.462148.

  71. Martino AT, Suzuki M, Markusic DM, Zolotukhin I, Ryals RC, Moghimi B, et al. The genome of self-complementary adeno-associated viral vectors increases Toll-like receptor 9-dependent innate immune responses in the liver. Blood. 2011;117:6459–68.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  72. Faust SM, Bell P, Cutler BJ, Ashley SN, Zhu Y, Rabinowitz JE, et al. CpG-depleted adeno-associated virus vectors evade immune detection. J Clin Investig. 2013;123:2994–3001.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  73. Xiang Z, Kurupati RK, Li Y, Kuranda K, Zhou X, Mingozzi F, et al. The Effect of CpG sequences on capsid-specific CD8(+) T cell responses to AAV vector gene transfer. Mol Ther. 2020;28:771–83.

    Article  CAS  PubMed  Google Scholar 

  74. Bertolini TB, Shirley JL, Zolotukhin I, Li X, Kaisho T, Xiao W, et al. Effect of CpG depletion of vector genome on CD8(+) T cell responses in AAV gene therapy. Front Immunol. 2021;12:672449.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Chan YK, Wang SK, Chu CJ, Copland DA, Letizia AJ, Costa Verdera H, et al. Engineering adeno-associated viral vectors to evade innate immune and inflammatory responses. Sci Transl Med. 2021;13:eabd3438.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  76. Konkle BA, Walsh CE, Escobar MA, Josephson NC, Young G, von Drygalski A, et al. BAX 335 hemophilia B gene therapy clinical trial results: potential impact of CpG sequences on gene expression. Blood. 2021;137:763–74.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  77. Ghemrawi R, Khair M. Endoplasmic reticulum stress and unfolded protein response in neurodegenerative diseases. Int J Mol Sci. 2020;21:6127.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  78. Prasad V, Greber UF. The endoplasmic reticulum unfolded protein response—homeostasis, cell death and evolution in virus infections. FEMS Microbiol Rev. 2021;45:fuab016.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Zolotukhin I, Markusic DM, Palaschak B, Hoffman BE, Srikanthan MA, Herzog RW. Potential for cellular stress response to hepatic factor VIII expression from AAV vector. Mol Ther Methods Clin Dev. 2016;3:16063.

    Article  PubMed  PubMed Central  Google Scholar 

  80. Balakrishnan B, Sen D, Hareendran S, Roshini V, David S, Srivastava A, et al. Activation of the cellular unfolded protein response by recombinant adeno-associated virus vectors. PLoS One. 2013;8:e53845.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  81. Buning H, Srivastava A. Capsid modifications for targeting and improving the efficacy of AAV vectors. Mol Ther Methods Clin Dev. 2019;12:248–65.

    Article  PubMed  PubMed Central  Google Scholar 

  82. Domenger C, Grimm D. Next-generation AAV vectors-do not judge a virus (only) by its cover. Hum Mol Genet. 2019;28:R3–14.

    Article  CAS  PubMed  Google Scholar 

  83. Monteys AM, Hundley AA, Ranum PT, Tecedor L, Muehlmatt A, Lim E, et al. Regulated control of gene therapies by drug-induced splicing. Nature. 2021;596:291–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. Geisler A, Fechner H. MicroRNA-regulated viral vectors for gene therapy. World J Exp Med. 2016;6:37–54.

    Article  PubMed  PubMed Central  Google Scholar 

  85. Sinnett SE, Boyle E, Lyons C, Gray SJ. Engineered microRNA-based regulatory element permits safe high-dose miniMECP2 gene therapy in Rett mice. Brain. 2021;144:3005–19.

    Article  PubMed  PubMed Central  Google Scholar 

  86. Watson ZL, Ertel MK, Lewin AS, Tuli SS, Schultz GS, Neumann DM, et al. Adeno-associated virus vectors efficiently transduce mouse and rabbit sensory neurons coinfected with herpes simplex virus 1 following peripheral inoculation. J Virol. 2016;90:7894–901.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  87. Fooden J. Systematic review of the rhesus macaque, Macaca mulatta (Zimmermann, 1780). In: Fieldiana, vol. 96. Field Museum of Natural History, 2000, pp 1-180.

  88. Amato R, Gardin JF, Tooze JA, Cline JM. Organ weights in relation to age and sex in Cynomolgus Monkeys (Macaca fascicularis). Toxicol Pathol. 2022;50:574–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  89. Herndon JG, Tigges J, Klumpp SA, Anderson DC. Brain weight does not decrease with age in adult rhesus monkeys. Neurobiol Aging. 1998;19:267–72.

    Article  CAS  PubMed  Google Scholar 

  90. Dearing J, Conte A, Brooks C, AZImina A, Rivas R, Brich SM, et al. Characterization of enterovirus D68 infection in four nonhuman primate species. bioRxiv.org 2022. https://doi.org/10.1101/2022.04.16.487524

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Acknowledgements

We thank the members of the Jerome lab for thoughtful discussions.

Funding

Research in our laboratory is funded by NIH grants R21AI117519, R01AI132599, UM1 AI126623, amfAR, the Caladan Foundation, over 1600 individual donors, and, in part, by a developmental grant from the University of Washington Center for AIDS Research (CFAR), an NIH-funded program under award number P30 AI 027757, which is supported by the following NIH Institutes and Centers (NIAID, NCI, NIMH, NIDA, NICHD, NHLBI, NIA, NIGMS, and NIDDK), and in part by NIH/NCI Cancer Center Support Grant P30 CA015704.

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DS, MA, and KRJ conceived and wrote the paper.

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Correspondence to Daniel Stone, Martine Aubert or Keith R. Jerome.

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KRJ is a paid advisor and holds equity in Excision Biosciences, has sponsored research agreements with Excision Biosciences and Emendo Biotherapeutics, and is co-inventor of patents held by Fred Hutch regarding AAV-delivered gene therapy. DS and MA have sponsored research agreements with Excision Biosciences.

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Stone, D., Aubert, M. & Jerome, K.R. Adeno-associated virus vectors and neurotoxicity—lessons from preclinical and human studies. Gene Ther (2023). https://doi.org/10.1038/s41434-023-00405-1

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