Your browser doesn't support javascript.
loading
Early distribution of18 F-labeled AAV9 vectors in the cerebrospinal fluid after intracerebroventricular or intracisternal magna infusion in non-human primates.
Kumagai, Shinichi; Nakajima, Takeshi; Shimazaki, Kuniko; Kakiuchi, Takeharu; Harada, Norihiro; Ohba, Hiroyuki; Onuki, Yoshiyuki; Takino, Naomi; Ito, Mika; Sato, Makoto; Nakamura, Sachie; Osaka, Hitoshi; Yamagata, Takanori; Kawai, Kensuke; Muramatsu, Shin-Ichi.
Affiliation
  • Kumagai S; Department of Neurosurgery, Jichi Medical University, Tochigi, Japan.
  • Nakajima T; Department of Neurosurgery, Jichi Medical University, Tochigi, Japan.
  • Shimazaki K; Department of Neurosurgery, Jichi Medical University, Tochigi, Japan.
  • Kakiuchi T; Central Research Laboratory, Hamamatsu Photonics K.K., Shizuoka, Japan.
  • Harada N; Central Research Laboratory, Hamamatsu Photonics K.K., Shizuoka, Japan.
  • Ohba H; Central Research Laboratory, Hamamatsu Photonics K.K., Shizuoka, Japan.
  • Onuki Y; Department of Neurosurgery, Jichi Medical University, Tochigi, Japan.
  • Takino N; Division of Neurological Gene Therapy, Jichi Medical University, Tochigi, Japan.
  • Ito M; Division of Neurological Gene Therapy, Jichi Medical University, Tochigi, Japan.
  • Sato M; Department of Neurosurgery, Jichi Medical University, Tochigi, Japan.
  • Nakamura S; Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
  • Osaka H; Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
  • Yamagata T; Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
  • Kawai K; Department of Neurosurgery, Jichi Medical University, Tochigi, Japan.
  • Muramatsu SI; Division of Neurological Gene Therapy, Jichi Medical University, Tochigi, Japan.
J Gene Med ; 25(1): e3457, 2023 01.
Article in En | MEDLINE | ID: mdl-36278965
ABSTRACT

BACKGROUND:

The delivery of adeno-associated virus (AAV) vectors via the cerebrospinal fluid (CSF) has emerged as a valuable method for widespread transduction in the central nervous system. Although infusion into the cerebral ventricles is a common protocol in preclinical studies of small animals, the cisterna magna has been recognized as an alternative target for clinical studies because it can be reached in a less invasive manner using an intrathecal catheter via the subarachnoid space from a lumbar puncture.

METHODS:

We evaluated the early distribution of fluorine-18-labeled AAV9 vectors infused into the lateral ventricle or cisterna magna of four non-human primates using positron emission tomography. The expression of the green fluorescent protein was immunohistochemically determined.

RESULTS:

In both approaches, the labeled vectors diffused into the broad arachnoid space around the brain stem and cervical spinal cord within 30 min. Both infusion routes efficiently transduced neurons in the cervical spinal cord.

CONCLUSIONS:

For gene therapy that primarily targets the cervical spinal cord and brainstem, such as amyotrophic lateral sclerosis, cisterna magna infusion would be a feasible and effective administration method.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord / Genetic Therapy Type of study: Guideline Limits: Animals Language: En Journal: J Gene Med Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2023 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord / Genetic Therapy Type of study: Guideline Limits: Animals Language: En Journal: J Gene Med Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2023 Document type: Article Affiliation country: Japón