Immunometric assays using monoclonal antibodies

• US 4,376,110 A
• Filed: 08/04/1980
• Issued: 03/08/1983
• Est. Priority Date: 08/04/1980
• Status: Expired due to Term

• Current Assignee: Hybritech, Inc. (Danaher Corporation)
• Original Assignee: Hybritech, Inc. (Danaher Corporation)
• Inventors: David, Gary S., Greene, Howard E.
• Primary Examiner(s): Marantz, Sidney
• Application Number:
  US06/175,133
• Time in Patent Office: 946 Days
• Field of Search: 23/230 B, 424/12, 424/1, 424/8, 435/7
• US Class Current: 435/5
• CPC Class Codes: G01N 2470/04 Sandwich assay format
• CPC Class Codes: G01N 33/576 for hepatitis
• CPC Class Codes: G01N 33/577 involving monoclonal antibodies binding reaction mechanisms characterised by the use of monoclonal antibodies; monoclonal antibodies per se are classified with their corresponding antigens; G01N33/53 - G01N33/576 take precedence
• CPC Class Codes: G01N 33/58 involving labelled substances G01N33/53 takes precedence
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
• CPC Class Codes: Y10S 435/971 Capture of complex after antigen-antibody reaction

Abstract

"Two-site" or "sandwich" immunometric assay techniques for determination of the presence and/or concentration of antigenic substances in fluids using monoclonal antibodies. One monoclonal antibody is presented in a soluble labeled form and a second monoclonal antibody is presented bound to a solid carrier; the soluble and bound monoclonal antibodies may be the products of either the same or different cell lines. Each monoclonal antibody has an affinity for the antigenic substances of at least about 10⁸ liters/mole.

Claims

1. A process for the determination of the presence of concentration of an antigenic substance in a fluid comprising the steps:

(a) contacting a sample of the fluid with a measured amount of a soluble first monoclonal antibody to the antigenic substance in order to form a soluble complex of the antibody and antigenic substance present in said sample, said first monoclonal antibody being labelled;

(b) contacting the soluble complex with a second monoclonal antibody to the antigenic substance, said second monoclonal antibody being bound to a solid carrier, said solid carrier being insoluble in said fluid, in order to form an insoluble complex of said first monoclonal antibody, said antigenic substance and said second monoclonal antibody bound to said solid carrier;

(c) separating said solid carrier from the fluid sample and unreacted labelled antibody;

(d) measuring either the amount of labelled antibody associated with the solid carrier or the amount of unreacted labelled antibody; and

(e) relating the amount of labelled antibody measured with the amount of labelled antibody measured for a control sample prepared in accordance with steps (a)-(d), said control sample being known to be free of said antigenic substance, to determine the presence of antigenic substance in said fluid sample, or relating the amount of labelled antibody measured with the amount of labelled antibody measured for samples containing known amounts of antigenic substance prepared in accordance with steps (a)-(d) to determine the concentration of antigenic substance in said fluid sample, the first and second monoclonal antibodies having an affinity for the antigenic substance of at least about 10⁸ liters/mole.

2. A process according to claim 1 wherein said first monoclonal antibody is the product of a different cell line than said second monoclonal antibody.

3. A process according to claim 1 wherein said antigen has at least two identical binding sites and said first and second monoclonal antibodies are the product of the same cell line.

4. A process according to claims 1, 2 or 3 wherein the affinity is at least about 10⁹ liters/mole.

5. A process according to any of claims 1, 2 or 3 wherein said solid carrier resulting from step (d) is washed to separate the fluid sample from the carrier.

6. A process according to claim 5 wherein the solid carrier is washed with phosphate buffered saline.

7. A process according to claims 1, 2 or 3 wherein the antigenic substance is selected from the group consisting of IgE, hepatitis A, hepatitis B, hepatitis Non A/Non B, alphafetoprotein, carcinoembryonic antigen, insulin and human thyroid stimulating hormone.

8. A process according to claims 1, 2 or 3 wherein the labelled antibody is labelled with a member selected from the group consisting of a radioactive isotope, an enzyme and a fluorogenic material and said examination is by means selected from the group consisting of radiometric means, enzymatic means and fluorometric means.

9. A process according to claim 8 wherein said label is the radioactive isotope ¹²⁵ I.

10. A process for the determination of the presence of an antigenic substance in a fluid comprising the steps:

(a) simultaneously contacting a sample of the fluid with first and second monoclonal antibodies to said antigenic substance, each monoclonal antibody having an affinity for the antigenic substance of at least about 10⁸ liters/mole, said first monoclonal antibody being labelled and soluble in said fluid and being provided for in a measured amount and said second monoclonal antibody being bound to a solid carrier insoluble in said fluid, in order to form an insoluble complex of said first monoclonal antibody, said antigenic substance and said second antibody;

(b) separating said solid carrier from the fluid sample and unreacted labelled antibody;

(c) measuring either the amount of labelled antibody associated with the solid carrier or the amount of unreacted labelled antibody; and

(d) relating the amount of labelled antibody measured with the amount of labelled antibody measured for a control sample prepared in accordance with steps (a)-(c), said control sample being known to be free of said antigenic substance, to determine the presence of antigenic substance in said fluid sample, or relating the amount of labelled antibody measured with the amount of labelled antibody measured for samples containing known amounts of antigenic substance prepared in accordance with steps (a)-(d) to determine the concentration of antigenic substance in said fluid sample.

11. A process according to claim 10 wherein said first monoclonal antibody is the product of a different cell line than said second monoclonal antibody.

12. A process according to claim 10 wherein said antigenic substance has at least two identical binding sites and said first and second monoclonal antibodies are the product of the same cell line.

13. A process according to claims 10, 11 or 12 wherein the affinity is at least about 10⁹ liters/mole.

14. A process according to any of claims 10, 11 or 12 wherein said solid carrier resulting from step (b) is washed to separate the fluid sample from the carrier.

15. A process according to claim 14 wherein the solid carrier is washed with phosphate buffered saline.

16. A process according to claims 10, 11 or 12 wherein the antigenic substance is selected from the group consisting of IgE, hepatitis A, hepatitis B, hepatitis Non A/Non B, alphafetoprotein, carcinoembryonic antigen, insulin and human thyroid stimulating hormone.

17. A process according to claims 10, 11 or 12 wherein the labelled antibody is labelled with a member selected from the group consisting of a radioactive isotope, an enzyme and a fluorogenic material and said examination is by means selected from the group consisting of radiometric means, enzymatic means and fluorometric means.

18. A process according to claim 17 wherein said label is the radioactive isotope ¹²⁵ I.

19. In an immunometric assay to determine the presence or concentration of an antigenic substance in a sample of a fluid comprising forming a ternary complex of a first labelled antibody, said antigenic substance, and a second antibody said second antibody being bound to a solid carrier insoluble in said fluid wherein the presence of the antigenic substance in the samples is determined by measuring either the amount of labelled antibody bound to the solid carrier or the amount of unreacted labelled antibody, the improvement comprising employing monoclonal antibodies having an affinity for the antigenic substance of at least about 10⁸ liters/mole for each of said labelled antibody and said antibody bound to a solid carrier.

20. A process according to claim 19 wherein the fluid sample is first contacted with the second monoclonal antibody to form a binary complex of the antigenic substance and said second monoclonal antibody insoluble in the fluid and then contacted with said first labelled monoclonal antibody to form the ternary complex.

21. A process according to claim 19 wherein the fluid sample is first contacted with the second monoclonal antibody to form a binary complex of the antigenic substance and said second monoclonal antibody insoluble in the fluid;

the sample separated from the solid carrier and the solid carrier contacted with a solution of said first labelled monoclonal antibody to form said ternary complex.

22. A process according to claim 21 wherein said solid carrier after formation of the ternary complex is washed to separate the fluid sample from the carrier.

23. A process according to claim 22 wherein the solid carrier is washed with phosphate buffered saline.

24. A process according to claims 19, 20 or 21 wherein said first monoclonal antibody is the product of a different cell line than said second monoclonal antibody.

25. A process according to claims 19, 20 or 21 wherein said antigen has at least two identical binding sites and said first and second monoclonal antibodies are the product of the same cell line.

26. A process according to claims 19, 20 or 21 wherein the affinity is at least about 10⁹ liters/mole.

27. A process according to claims 19, 20 or 21 wherein the antigen is selected from the group consisting of IgE, hepatitis A, hepatitis B, hepatitis None A/Non B, alphafetoprotein, carcinoembryonic antigen, insulin and human thyroid stimulating hormone.

28. A process according to claims 19, 20 or 21 wherein the labelled antibody is labelled with a member selected from the group consisting of a radioactive isotope, an enzyme and a fluorogenic material.

29. A process according to claim 28 wherein said label is the radioactive isotope ¹²⁵ I.