Therapeutic vaccine for the treatment of papillomavirus lesions
Abstract
An attenuated vaccinia virus GAB-1 and its use in a vaccine for treatment of papillomavirus lesions is described. In preferred embodiments, the Lederle-Chorioallantoic strain of vaccinia virus is serially passaged in chicken embryo-fibroblast (CEF) cells by at least 100 passages. GAB-1 has reduced virulence and is safe to use without side effects after attenuation by serial passaging, but remains highly immunogenic. Experimentation has found that GAB-1 is much more immunogenic than other strains of vaccinia virus, including Western Reserve (WR) and modified Vaccinia Ankara (MVA). GAB-1 can be used safely in humans for treating tumorous lesions caused by human papillomavirus (HPV).
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A viral preparation, comprising an attenuated Lederle-Chorioallantoic strain of vaccinia virus that has been serially passaged in a host cell.
2 . The viral preparation of claim 1 , wherein the host cell is selected from the group consisting of chicken embryo fibroblast (CEF) cells, a monkey kidney cell line (VERO), and a monkey epithelial cell line (BSC-1).
3 . The viral preparation of claim 1 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus produces more viral particles in an animal cell than does a wildtype Western Reserve strain of vaccinia virus.
4 . The viral preparation of claim 1 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus produces morphologic plaques, but not lytic plaques in chicken embryo fibroblast (CEF).
5 . The viral preparation of claim 1 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus has been passaged in chicken embryo fibroblast (CEF) cells for at least 100 passages.
6 . The viral preparation of claim 5 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus has been serially passaged in CEF cells for at least 200 passages.
7 . The viral preparation of claim 1 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus has lost at least 5000 base pairs of nucleotides after serial passaging.
8 . The viral preparation of claim 7 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus has been passaged in chicken embryo fibroblast (CEF) cells for at least 100 passages.
9 . The viral preparation of claim 7 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus has lost between 8,000 and 12,000 base pairs of nucleotides after serial passaging.
10 . The viral preparation of claim 9 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus has been serially passaged in chicken embryo fibroblast (CEF) cells for at least 200 passages.
11 . The viral preparation of claim 1 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus protects an animal from wildtype Western Reserve strain of vaccinia virus.
12 . The viral preparation of claim 1 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus is at effective in reducing size of cervical intraepithelial neoplasia by at least 80%.
13 . The viral preparation of claim 1 , wherein the attenuated Lederle-Chorioallantoic strain of vaccinia virus generates more viral particles in a host than does modified vaccinia Ankara (MVA) E2 strain of vaccinia virus.
14 . The viral preparation of claim 1 , wherein the Lederle-Chorioallantoic strain of vaccinia virus produces a higher antibody titer than does a modified vaccinia Ankara (MVA) E2 strain of vaccinia virus in a patient.
15 . The viral preparation of claim 1 , wherein the Lederle-Chorioallantoic strain of vaccinia virus produces a higher antibody titer than does wildtype Western Reserve strain of vaccinia virus in an animal.Join the waitlist — get patent alerts
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