» Articles » PMID: 9917091

Distribution, Persistency, Toxicity, and Lack of Replication of an E1A-deficient Adenoviral Vector After Intracardiac Delivery in the Cotton Rat

Overview
Date 1999 Jan 23
PMID 9917091
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Adenoviral vectors were inoculated via intracardiac injection into 5- to 1O-week-old cotton rats (Sigmodon hispidus) to evaluate the effects of systemic delivery. Cotton rats were chosen as a model because they are semipermissive to the replication of human adenoviruses. The vector used was AdV.RSV-tk, a replication-deficient adenovirus with a herpes simplex virus thymidine kinase gene inserted in the E1 region. Vector doses were 3 x 10(8), 3 x 10(9), and 3 x 10(10) viral particles per animal with and without ganciclovir at 10 mg/kg twice a day. Animals were sacrificed and necropsied at 24 hours, 7 days, and 14 days postinoculation. Gross and microscopic pathologic observations in dosed groups were compared with an unmanipulated control group. From each animal, 10 different organ systems were analyzed for histopathology and vector distribution. The only significant microscopic lesions observed were epicardial inflammation and splenic hemosiderosis. Vector sequences persisted throughout the 14-day assay with preponderance in the heart, lung, and lymphoid organs. Infectious virions were detected for 24 hours, and these virions were only detected at the site of injection of two animals in the highest dose group. No viral replication was detected. Therefore, systemic delivery of up to 3 x 10(11) viral particles/kg was well tolerated in this semipermissive host model and did not result in any significant pathology.

Citing Articles

Immunotherapy and gene therapy as novel treatments for cancer.

Rangel-Sosa M, Aguilar-Cordova E, Rojas-Martinez A Colomb Med (Cali). 2017; 48(3):138-147.

PMID: 29213157 PMC: 5687866. DOI: 10.25100/cm.v48i3.2997.


A novel immunocompetent murine tumor model for the evaluation of RCAd-enhanced RDAd transduction efficacy.

Wang H, Wei F, Zhang J, Wang F, Li H, Chen X Tumour Biol. 2012; 33(4):1245-53.

PMID: 22627833 DOI: 10.1007/s13277-012-0374-7.


Immunocompetent syngeneic cotton rat tumor models for the assessment of replication-competent oncolytic adenovirus.

Steel J, Morrison B, Mannan P, Abu-Asab M, Wildner O, Miles B Virology. 2007; 369(1):131-42.

PMID: 17727912 PMC: 2104792. DOI: 10.1016/j.virol.2007.07.022.


The combination of adenoviral HSV TK gene therapy and radiation is effective in athymic mouse glioblastoma xenografts without increasing toxic side effects.

Nestler U, Wakimoto H, Siller-Lopez F, Aguilar L, Chakravarti A, Muzikansky A J Neurooncol. 2004; 67(1-2):177-88.

PMID: 15072465 DOI: 10.1023/b:neon.0000021897.53969.ca.


Evolution of a gene therapy clinical trial. From bench to bedside and back.

Aguilar L, Aguilar-Cordova E J Neurooncol. 2003; 65(3):307-15.

PMID: 14682380 DOI: 10.1023/b:neon.0000003659.04633.6e.