Measuring circulating therapeutic antibody, antigen and antigen/antibody complexes using ELISA assays
US-9157916-B2 · Oct 13, 2015 · US
US10018638B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10018638-B2 |
| Application number | US-201715606877-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 26, 2017 |
| Priority date | Sep 20, 2001 |
| Publication date | Jul 10, 2018 |
| Grant date | Jul 10, 2018 |
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The present invention relates to the field of immunology and hyperproliferative diseases. More specifically, the present invention relates to a method of detecting and monitoring therapeutic antibody:antigen complex, soluble antigen and soluble therapeutic antibody, wherein a patient has undergone at least one course of immunotherapy. Yet further, levels of therapeutic antibody:antigen complexes, soluble antigens or soluble therapeutic antibodies may be measured and used to stage or monitor a hyperproliferative disease.
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What is claimed is: 1. A method for determining a dosage of a therapeutic anti-CD20 antibody for treating B cell hyperproliferative disease, the method comprising testing a sample from a human to measure the level of soluble CD20, and determining the dosage of the therapeutic anti-CD20 antibody according to the level of soluble CD20. 2. The method of claim 1 , wherein said sample is selected from the group consisting of plasma, serum, and cell lysate. 3. The method of claim 1 , wherein said therapeutic anti-CD20 antibody is Rituximab. 4. The method of claim 1 , wherein said B-cell hyperproliferative disease is chronic lymphocytic leukemia, acute lymphoblastic leukemia, myelodysplastic syndrome, chronic myelomonocytic leukemia, juvenile myelomonocyte leukemia, multiple myeloma, hairy cell leukemia, prolymphocytic leukemia, or lymphoma. 5. The method of claim 4 , wherein said B-cell hyperproliferative disease is chronic lymphocytic leukemia. 6. The method of claim 1 , further comprising administering said therapeutic anti-CD20 antibody to said human. 7. The method of claim 3 , further comprising administering said Rituximab to said human.
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