Methods for identifying subjects at risk of thrombosis or malignancy
AssigneeThe Johns Hopkins University
InventorsEduardo Gómez-Bañuelos, Felipe Andrade
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Abstract
Disclosed herein are methods for detecting or determining an amount, quantity, concentration and/or level of an anti-transcription factor A, mitochondrial (TFAM) antibody, such as an anti-human TFAM antibody, in one or more biologics samples obtained from a subject. In some aspects, the methods relate to identifying a subject suffering from systemic lupus erythematosus (SLE) and/or antiphospholipid syndrome that is at risk of thrombosis, malignancy, death or any combination thereof.
Claims16
A method of identifying a subject suffering from systemic lupus erythematosus (SLE) that is at risk of thrombosis or malignancy, the method comprising the steps of:
- a. contacting at least one biological sample obtained from a subject suffering from SLE with:
- i. at least one first specific binding partner, wherein the at least one first specific binding partner comprises a polypeptide comprising amino acids 43 to 246 of mature human transcription factor A, mitochondrial (TFAM), and further wherein at least one anti-TFAM antibody in the sample specifically binds to the polypeptide, and
- ii. at least one type of second specific binding partner comprising a detectable label, wherein the second specific binding partner specifically binds to at least one anti-TFAM antibody in the sample, thereby producing one or more types of first complexes comprising the first specific binding partner-anti-TFAM antibody-second specific binding partner;
- b. assessing a signal from one or more types of first complexes, wherein the amount of detectable signal from the detectable label indicates the amount of at least one anti-TFAM antibody in the sample;
- and
- c. identifying the subject as at risk of thrombosis or for malignancy if the amount of first complexes in the sample higher than a reference level or not at risk of thrombosis or for malignancy if the amount of first complexes in the sample is equal to or lower than a reference level, wherein the reference level is based on the amount of first complexes detected in a control group of human subjects who do not suffer from SLE.
Dependencies are inferred from the claim text.