Rabbit monoclonal antibodies to hepatitis B surface antigens and methods of using the same
View Patent ↗Reagents, methods and immunodiagnostic test kits for the accurate detection of hepatitis B virus (HBV) infection are disclosed. The methods and kits employ novel rabbit monoclonal antibodies directed against HBV surface antigens (HBsAg) with mutations in the “a” determinant region of HBsAg.
1. A method of detecting HBV surface antigens (HBsAgs) in a biological sample, comprising:
(a) contacting said biological sample with at least one rabbit monoclonal antibody, wherein said at least one rabbit monoclonal antibody is produced by Hybridoma 99S6 (ATCC Accession number PTA-6015) or Hybridoma 99S9 (ATCC Accession number PTA-6014) or recognizes the same epitope as an antibody produced by Hybridoma 99S6 (ATTC Accession No. PTA-6015) or Hybridoma 99S9 (ATCC Accession No. PTA-6014), under conditions which allow HBV antigens, when present in the biological sample, to bind to said antibody to form an antibody/HBsAg complex; and
(b) detecting the presence or absence of said antibody/HBsAg complex, thereby detecting the presence or absence of HBV surface antigens in said sample.
2. A method of detecting the presence of HBV surface antigens (HBsAgs) in a biological sample, said method comprising:
(a) providing a biological sample;
(b) providing a solid support comprising at least one rabbit monoclonal antibody or an immunoreactive Fab or F(ab′) 2 fragment thereof, wherein:
said at least one rabbit monoclonal antibody is produced by Hybridoma 99S6 (ATCC Accession number PTA-6015) or Hybridoma 99S9 (ATCC Accession number PTA-6014) or recognizes the same epitope as an antibody produced by Hybridoma 99S6 (ATTC Accession No. PTA-6015) or Hybridoma 99S9 (ATCC Accession No. PTA-6014); and
the immunoreactive fragment thereof recognizes the same epitope as an antibody produced by Hybridoma 99S6 (ATTC Accession No. PTA-6015) or Hybridoma 99S9 (ATCC Accession No. PTA-6014);
(c) contacting said biological sample with said solid support, under conditions which allow HBV surface antigens, if present in the biological sample, to bind with at least one of the rabbit monoclonal antibodies to form an antibody/HBsAg complex; and
(d) detecting the presence of the antibody/HBsAg complex, thereby detecting the presence of HBV surface antigens in the biological sample.
3. A method of detecting the presence of anti-HBsAg antibodies in a biological sample, said method comprising:
(a) providing a solid support comprising at least one rabbit monoclonal antibody or an immunoreactive Fab or F(ab′) 2 fragment thereof, wherein:
said at least one rabbit monoclonal antibody is produced by Hybridoma 99S6 (ATCC Accession number PTA-6015) or Hybridoma 99S9 (ATCC Accession number PTA-6014) or recognizes the same epitope as an antibody produced by Hybridoma 99S6 (ATTC Accession No. PTA-6015) or Hybridoma 99S9 (ATCC Accession No. PTA-6014); and
the immunoreactive fragment thereof recognizes the same epitope as an antibody produced by Hybridoma 99S6 (ATTC Accession No. PTA-6015) or Hybridoma 99S9 (ATCC Accession No. PTA-6014);
(b) contacting said solid support with one or more HBsAgs, under conditions which allow the one or more HBsAgs to bind with at least one of the rabbit monoclonal antibodies to form an antibody/HBsAg complex;
(c) contacting said solid support having said antibody/HBsAg complex with a biological sample, under conditions which allow anti-HBsAg antibodies, if present in the biological sample, to bind with said antibody/HBsAg complex to form an antibody/HBsAg/antibody complex; and
(d) detecting the presence of the antibody/HBsAg/antibody complex, thereby detecting the presence of anti-HBsAg antibodies in the biological sample.
4. The method of claim 1 , 2 or 3 , wherein said at least one rabbit monoclonal antibody is produced by Hybridoma 99S6 (ATCC Accession number PTA-6015) or Hybridoma 99S9 (ATCC Accession number PTA-6014).
5. The method of claim 1 , wherein said at least one rabbit monoclonal antibody is detectably labeled.
6. The method of claim 1 , wherein the method further comprises reacting said biological sample with one or more additional antibodies directed against a wild-type HBsAg or an HBsAg mutant with a mutation in the “a” determinant region.
7. The method of claim 5 , wherein the one or more additional antibodies comprise an additional monoclonal antibody.
8. The method of claim 6 , wherein the one or more additional antibodies comprise a mouse monoclonal antibody.
9. The method of claim 2 , further comprising:
(e) removing unbound HBV antigens;
(f) providing one or more moieties capable of associating with said antibody/antigen complex; and
(g) detecting the presence of said one or more moieties, thereby detecting the presence of HBV surface antigens in the biological sample.
10. The method of claim 9 , wherein said one or more moieties comprises a detectably labeled HBV antibody.
11. The method of claim 10 , wherein said detectably labeled HBV antibody is a rabbit monoclonal antibody that recognizes an HBsAg mutant with a mutation in the “a” determinant region, or an immunoreactive fragment thereof.
12. The method of claim 10 , wherein the detectable label is an enzyme.
13. The method of claim 2 , wherein said biological sample is from a human blood sample.
14. The method of claim 3 , further comprising:
(e) removing unbound antibodies;
(f) providing one or more moieties capable of associating with said antibody/antigen/antibody complex; and
(g) detecting the presence of said one or more moieties, thereby detecting the presence of anti-HBsAg antibodies in the biological sample.
15. The method of claim 14 , wherein said one or more moieties comprises a detectably labeled immunoglobulin molecule.
16. A method of preparing a blood supply comprising whole blood, platelets, plasma or serum, substantially free of HBV comprising:
(a) screening aliquots of whole blood, platelets, plasma or serum from collected blood samples by the method of claim 13 ;
(b) eliminating any samples in which an HBV antigen is detected; and
(c) combining samples in which no HBV antigen is detected to provide a blood supply substantially free of HBV.
17. A method of preparing a blood supply comprising whole blood, platelets, plasma or serum, substantially free of HBV comprising:
(a) screening aliquots of whole blood, platelets, plasma or serum from collected blood samples by the method of claim 14 ;
(b) eliminating any samples in which an anti-HBsAg antibody is detected; and
(c) combining samples in which no anti-HBsAg antibody is detected to provide a blood supply substantially free of HBV.
18. A method of screening a donated tissue or organ prior to transplantation to provide a tissue or organ substantially free of HBV comprising:
(a) screening a sample from said tissue or organ by the method of claim 2 ;
(b) eliminating a tissue or organ in which an HBV antigen is detected to provide a tissue or organ substantially free of HBV.
19. A method of screening a donated tissue or organ prior to transplantation to provide a tissue or organ substantially free of HBV comprising:
(a) screening a sample from said tissue or organ by the method of claim 14 ; and
(b) eliminating a tissue or organ in which an anti-HBsAg antibody is detected to provide a tissue or organ substantially free of HBV.