AAV2-mediated gene delivery to monkey putamen: evaluation of an infusion device and delivery parameters - PubMed (original) (raw)

. 2005 Aug;194(2):476-83.

doi: 10.1016/j.expneurol.2005.03.007.

Jurg M Sommer, Brian M Suzuki, Peter H Smith, Sharmila Vijay, Joseph A Vargas, John R Forsayeth, Janet Cunningham, Krys S Bankiewicz, Haihwa Kao, Jan Bernal, Glenn F Pierce, Kirk W Johnson

Affiliations

AAV2-mediated gene delivery to monkey putamen: evaluation of an infusion device and delivery parameters

Laura M Sanftner et al. Exp Neurol. 2005 Aug.

Abstract

In this study, a modified infusion procedure and a novel infusion device designed for use in humans (Clinical Device B) were evaluated for delivery of recombinant adeno-associated virus (AAV2) to brain. The device is composed of 1.2 m of fused silica inserted through a 24.6-cm surgical steel cannula designed to fit a standard Leksell clinical stereotaxic frame and micro-infusion syringe pump. AAV2 encoding the human aromatic l-amino acid decarboxylase gene (AAV-hAADC-2) was infused into the putamen of 4 normal rhesus monkeys as a supportive study for a clinical trial in Parkinson's disease (PD) patients. Two infusion protocols were tested: a ramped procedure (slow stepwise increases in rate from 0.2 muL/min to 1 muL/min), thought to be essential for convection-enhanced delivery (CED), and a non-ramped infusion at a constant rate of 1 muL/min. The primary endpoints were safety evaluation of the infusion procedures and assessment of transgene expression at 5.5 weeks post-infusion. Clinical observations after vector infusions revealed no behavioral abnormalities during the study period. No differences in gross pathology with either the ramped or non-ramped infusion procedure were observed. Histopathology of the putamen was comparable with both procedures, and revealed only minimal localized inflammatory tissue reaction along the needle track in response to cannula placement and vector infusion. AADC immunohistochemistry demonstrated that vector was distributed throughout the putamen, with no significant difference in volume of immunostaining with either infusion procedure. Serum antibody levels against AAV2 vector exhibited a minor increase after infusion. These results validate the clinical utility of this new infusion device and non-ramped infusion conditions for intraputamenal gene therapy, and have the potential to impact a number of human diseases in which delivery of therapeutics to brain is indicated.

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Figures

Fig. 1

Fig. 1

AAV vector infusion device designed for human clinical use. The cannula (formula image) is composed of 4 layers of 304 surgical steel fused together by laser welding in a step design, ending in 23-gauge tubing. The steel cannula is lined with fused silica of 100 Am inner diameter (formula image, red) which also forms the tip of the delivery device by extending 1 cm beyond the steel. Approximately 1.2 m of additional fused silica covered with Teflon tubing (formula image, blue) connect to a Luer hub (formula image). A 1-in., 23-gauge steel spacer (formula image) between the fused silica and Teflon tubing is sealed and attached to the Luer hub with medical grade cyanoacrylate glue. Dimensions are in centimeters.

Fig. 2

Fig. 2

Immunohistochemistry for AADC in whole mounted brain sections. Brains are shown in coronal section through the infusion site at 5.5 weeks post-infusion. Panels A, B, C, and D represent the four different monkey brains analyzed in this study [MR15102M (A), MR15109M (B), R23700M (C), and R211101M (D)]. All left hemispheres received ramped infusion and all right hemispheres received non-ramped infusion. The black arrow indicates the putamen region.

Fig. 3

Fig. 3

Immunohistochemistry for AADC at high magnification within the putamen. Immunostaining is localized to the medium spiny neurons in the putamen at 5.5 weeks post-infusion. A representative section from the hemisphere that received ramped infusion is shown in Panel A and one from the hemisphere that received non-ramped infusion is shown in Panel B. Scale bar = 100 μm.

Fig. 4

Fig. 4

H&E-stained sections within the putamen from a representative animal, R211101M, at 5× magnification. Animal R211101M received bilateral CED of AAV-hAADC-2 using the non-ramped infusion procedure in the right hemisphere (Panel A) and the ramped infusion procedure in the left hemisphere (Panel B). Images illustrate the area adjacent to the cannula track, and were taken at the mid-caudal putamen level. Scale bar = 400 μm.

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