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Title: NANBV diagnostics and vaccines
United States Patent: 6,346,375
Inventors: Chien; David Y. (Alamo, CA)
Assignee: Chiron Corporation (Emeryville, CA)
Appl. No.: 403590
Filed: March 14, 1995
Abstract
We have discovered epitopes of the HCV viral proteins which are
immunoreactive with immune serum. The epitopes are useful in
immunodiagnostic assays and as immunogens.
DISCLOSURE OF THE INVENTION
The invention pertains to the isolation and
characterization of a newly discovered etiologic agent of NANBH, hepatitis
C virus (HCV), its nucleotide sequences, its protein sequences and
resulting polynucleotides, polypeptides and antibodies derived therefrom.
The inventions described herein were made possible by the discovery of
cDNA replicas isolated by a technique which included a novel step of
screening expression products from cDNA libraries created from a
particulate agent in infected tissue with sera from patients with NANBH to
detect newly synthesized antigens derived from the genome of the
heretofore unisolated and uncharacterized viral agent, and of selecting
clones which produced products which reacted immunologically only with
sera from infected individuals as compared to non-infected individuals.
Studies of the nature of the genome of the HCV, utilizing probes derived
from the HCV cDNA, as well as sequence information contained within the
HCV cDNA, are suggestive that HCV is a positive-stranded RNA virus which
appears to be distantly related to the flaviviridae family, and to the
pestiviruses.
Portions of the cDNA sequences derived from HCV are useful as probes to
diagnose the presence of virus in samples, and to isolate naturally
occurring variants of the virus. These cDNAs also make available
polypeptide sequences of HCV antigens encoded within the HCV genome(s) and
permits the production of polypeptides which are useful as standards or
reagents in diagnostic tests and/or as components of vaccines. Antibodies,
including for example both polyclonal and monoclonal, directed against HCV
epitopes contained within these polypeptide sequences are also useful for
diagnostic tests, as therapeutic agents, for screening of antiviral
agents, and for the isolation of the NANBV agent from which these cDNAs
derive. In addition, by utilizing probes derived from these cDNAs it is
possible to isolate and sequence other portions of the HCV genome, thus
giving rise to additional probes and polypeptides which are useful in the
diagnosis and/or treatment, both prophylactic and therapeutic, of NANBH.
Accordingly with respect to polynucleotides, some aspects of the invention
are: a purified HCV polynucleotide; a recombinant HCV polynucleotide; a
recombinant polynucleotide comprising a sequence derived from an HCV
genome or from HCV cDNA; a recombinant polynucleotide encoding an epitope
of HCV; a recombinant vector containing any of the above recombinant
polynucleotides, and a host cell transformed with any of these vectors.
Other aspects of the invention are: a recombinant expression system
comprising an open reading frame (ORF) of DNA derived from an HCV genome
or from HCV cDNA, wherein the ORF is operably linked to a control sequence
compatible with a desired host, a cell transformed with the recombinant
expression system, and a polypeptide produced by the transformed cell.
Still other aspects of the invention are: purified HCV, a preparation of
polypeptides from the purified HCV; a purified HCV polypeptide; a purified
polypeptide comprising an epitope which is immunologically identifiable
with an epitope contained in HCV.
Included aspects of the invention are a recombinant HCV polypeptide; a
recombinant polypeptide comprised of a sequence derived from an HCV genome
or from HCV cDNA; a recombinant polypeptide comprised of an HCV epitope;
and a fusion polypeptide comprised of an HCV polypeptide.
Also included in the invention are a monoclonal antibody directed against
an HCV epitope; and a purified preparation of polyclonal antibodies
directed against an HCV epitope; and an anti-idiotype antibody comprising
a region which mimics an HCV epitope.
Another aspect of the invention is a particle which is immunogenic against
HCV infection comprising a non-HCV polypeptide having an amino acid
sequence capable of forming a particle when said sequence is produced in a
eukaryotic host, and an HCV epitope.
Still another aspect of the invention is a polynucleotide probe for HCV.
Aspects of the invention which pertain to kits are those for: analyzing
samples for the presence of polynucleotides derived from HCV comprising a
polynucleotide probe containing a nucleotide sequence from HCV of about 8
or more nucleotides, in a suitable container; analyzing samples for the
presence of an HCV antigen comprising an antibody directed against the HCV
antigen to be detected, in a suitable container; analyzing samples for the
presence of an antibodies directed against an HCV antigen comprising a
polypeptide containing an HCV epitope present in the HCV antigen, in a
suitable container.
Other aspects of the invention are: a polypeptide comprising an HCV
epitope, attached to a solid substrate; and an antibody to an HCV epitope,
attached to a solid substrate.
Still other aspects of the invention are: a method for producing a
polypeptide containing an HCV epitope comprising incubating host cells
transformed with an expression vector containing a sequence encoding a
polypeptide containing an HCV epitope under conditions which allow
expression of said polypeptide; and a polypeptide containing an HCV
epitope produced by this method.
The invention also includes a method for detecting HCV nucleic acids in a
sample comprising reacting nucleic acids of the sample with a probe for an
HCV polynucleotide under conditions which allow the formation of a
polynucleotide duplex between the probe and the HCV nucleic acid from the
sample; and detecting a polynucleotide duplex which contains the probe.
Still other aspects are also included in the invention. These include an
immunoassay for detecting an HCV antigen comprising incubating a sample
suspected of containing an HCV antigen with a probe antibody directed
against the HCV antigen to be detected under conditions which allow the
formation of an antigen-antibody complex; and detecting an
antigen-antibody complex containing the probe antibody. An immunoassay for
detecting antibodies directed against an HCV antigen comprising incubating
a sample suspected of containing anti-HCV antibodies with a probe
polypeptide which contains an epitope of the HCV, under conditions which
allow the formation of an antibody-antigen complex; and detecting the
antibody-antigen complex containing the probe antigen.
Also included in the invention are vaccines for treatment of HCV infection
comprising an immunogenic peptide containing an HCV epitope, or an
inactivated preparation of HCV, or an attenuated preparation of HCV.
Another aspect of the invention is a tissue culture grown cell infected
with HCV.
Yet another aspect of the invention is a method for producing antibodies
to HCV comprising administering to an individual an isolated immunogenic
polypeptide containing an HCV epitope in an amount sufficient to produce
an immune response.
Claim 1 of 9 Claims
What is claimed is:
1. An octamer polypeptide immunoreactive with an HCV antibody, wherein the
octamer has the amino acid sequence shown at positions 2280 to 2287
(AA2280-AA2287) as set forth in FIG. 72 (SEQ ID NOS:137-138).
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