IP Library Granted Patent US 12,681,016
Granted Patent B2
US 12,681,016 · App. 18/530,800 · Granted Jul 14, 2026

Compositions and methods for detecting autoantibodies

Inventors: Yunsheng Li (Athens, OH); Paul D. Olivo (St. Louis, MO); Hannah Jaekyung Kim (Athens, OH)
Assignee: ORTHO-CLINICAL DIAGNOSTICS, INC.
G01N33/564G01N33/566G01N33/76G01N2333/723G01N2333/726G01N2800/046
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Quick Facts
Patent No.
US 12,681,016
App. No.
18/530,800
Granted
Jul 14, 2026
Kind
B2
Abstract

The invention provides compositions and methods for detecting thyroid hormone blocking immunoglobulin (TBI). The invention's methods are sensitive and specific for TBI, and may be used for the dual detection of both TBI and TSI. The invention's compositions and methods are useful for the diagnosis of diseases that are associated with the presence of TBI and/or TSI, for monitoring the progress of disease and/or treatment regimens, therapeutics, vaccines, etc., and for assisting clinicians in making treatment decisions.

Claims (44)

1 . A method for detecting thyroid hormone blocking immunoglobulin (TBI) in a sample, comprising:

a) combining each of a biological sample from a subject and a control sample with

i) transgenic cells stably or transiently transfected with one or more expression vectors comprising

1) A first nucleic acid sequence that encodes a reporter, wherein said first nucleotide sequence is operably linked to a CAMP-inducible promoter, and

2) The nucleotide sequence of SEQ ID NO: 2 that encodes a chimeric TSH receptor (TSHR), wherein said SEQ ID NO: 2 is operably linked to a constitutive promoter,

wherein said cells express said chimeric TSHR on the cell membrane, and

ii) a thyroid stimulating polypeptide that stimulates said chimeric TSHR upon binding to said TSHR, wherein said thyroid stimulating polypeptide is selected from the group consisting of thyroid stimulating hormone (TSH), a thyroid stimulating monoclonal antibody, and thyroid stimulating polyclonal antibody,

wherein said combining said transgenic cells and said thyroid stimulating polypeptide with

A) said control sample produces a first sample, and

B) said biological sample produces a second sample, and

is under conditions for binding of said thyroid stimulating polypeptide to said chimeric TSHR, and

b) measuring the level of expression of said reporter in said first sample and in said second sample, wherein a reduced level of expression of said reporter in said second sample compared to said first sample indicates the presence of TBI in said test sample.

2 . The method of claim 1 , wherein the IC 50 for TBI is from 5 fold to 15 fold smaller than the IC 50 for TBI when the method is performed with said transgenic cells in which chimeric TSHR is substituted with wild type TSHR.

3 . The method of claim 1 , wherein the IC 50 for TBI is from 10 fold to 30 fold smaller when the thyroid stimulating polypeptide is TSH than when the thyroid stimulating polypeptide is an anti-TBI monoclonal antibody.

4 . The method of claim 1 , wherein said method further comprises detecting a reduced level of expression of said reporter in said second sample compared to said first sample.

5 . The method of claim 1 , wherein said method further comprises determining the level of TBI in said test sample by comparing

a) the level of expression of said reporter after said contacting with said biological sample, with

b) the level of expression of said reporter after contacting said transgenic cells with one or more standard samples, each containing a known concentration of TSH.

6 . The method of claim 1 , wherein said thyroid stimulating polypeptide is TSH.

7 . The method of claim 6 , wherein said TSH is bovine TSH.

8 . The method of claim 1 , wherein said reporter comprises a bioluminescence protein.

9 . The method of claim 1 , wherein said transgenic cells are Chinese hamster ovary (CHO) cells or human Rhabdomyosarcoma (RD) cells.

10 . The method of claim 1 , wherein said biological sample is a serum sample.

11 . A method for detecting thyroid hormone blocking immunoglobulin (TBI) and thyroid hormone stimulating immunoglobulin (TSI) in a biological sample, comprising:

a) combining each of a biological sample and a control sample with

i) transgenic cells stably or transiently transfected with one or more expression vectors comprising a

1) A first nucleic acid sequence that encodes a reporter, wherein said first nucleic acid sequence is operably linked to a cAMP-inducible promoter, and

2) The nucleotide sequence of SEQ ID NO: 2 that encodes a chimeric TSH receptor (TSHR), wherein said SEQ ID NO: 2 is operably linked to a constitutive promoter,

wherein said cells express said chimeric TSHR on the cell membrane, and

ii) a thyroid stimulating polypeptide,

wherein said combining said transgenic cells and said thyroid stimulating polypeptide with

A) said control sample produces a first sample, and

B) said biological sample produces a second sample, and

is under conditions for binding of said thyroid stimulating polypeptide to said chimeric TSHR, and

b) measuring the level of expression of said reporter in said transgenic cells before said combining and after said combining, wherein

i) a reduced level of expression of said reporter in said second sample compared to said first sample indicates the presence of TBI in said test sample,

and

ii) an increased level of expression of said reporter in said second sample compared to said first sample indicates the presence of TSI in said test sample.

12 . The method of claim 11 , wherein said method further comprises detecting a reduced level of expression of said reporter in said second sample compared to said first sample, wherein said detecting of a reduced level of expression of said reporter indicates the presence of TBI in said biological sample.

13 . The method of claim 11 , wherein said transgenic cells are Chinese hamster ovary (CHO) cells or human Rhabdomyosarcoma (RD) cells.

14 . The method of claim 11 , wherein said thyroid stimulating polypeptide is TSH.

15 . The method of claim 14 , wherein said TSH is bovine TSH.

16 . The method of claim 11 , wherein said reporter comprises a bioluminescence protein.

17 . The method of claim 11 , wherein said biological sample is a serum sample.

Assignments (3)
SECURITY AGREEMENT Recorded Aug 22, 2025
From: CRIMSON INTERNATIONAL ASSETS LLC; MICRO TYPING SYSTEMS, INC.; ORTHO-CLINICAL DIAGNOSTICS, INC.; QUIDEL CARDIOVASCULAR INC.
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 072526/0643 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 15, 2024
From: QUIDEL CORPORATION
To: ORTHO-CLINICAL DIAGNOSTICS, INC.
Reel/Frame 068657/0827 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2024
From: LI, YUNSHENG; OLIVO, PAUL D.; KIM, JACKYUNG
To: QUIDEL CORPORATION
Reel/Frame 067856/0990 →
Continuity (4)
Continuation 16871554 · May 11, 2020
Division 14625086 · Feb 18, 2015
Continuation 13228705 · Sep 9, 2011
Related Publication 20240133882A1 · Apr 25, 2024
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