Detection of glucuronidated and 3-bromotyrosine
The present invention to provides methods, kits, and compositions for: i) detecting the level of 3-bromotyrosine in a sample that has been treated to liberate 3-bromotyrosine from 4-O-glucuronide-3-bromotyrosine, and/or ii) detecting the level of 4-O-glucuronide-3-bromotyrosine, and/or the combined level of both 4-O-glucuronide-3-bromotyrosine and 3-bromotyrosine, in a sample that has not been treated to liberate 3-bromotyrosine from 4-O-glucuronide-3-bromotyrosine. In certain embodiments, such detected levels are used to: i) identify the presence, severity, or risk of an eosinophilic disorder (e.g., asthma or a TH2-high eosinophilic disorder); ii) identify therapy effective for treating asthma or an eosinophilic disorder; or iii) identify patients suitable for treatment with therapeutic agents targeted to asthma or an eosinophilic disorder.
1. A method of testing a sample comprising:
testing a sample from a human subject to determine the level of 3-bromotyrosine, wherein said sample has been treated to liberate 3-bromotyrosine from 4-O-glucuronide-3-bromotyrosine; and
wherein said sample is selected from the group consisting of: urine, saliva, serum, plasma, tissue biopsy, and whole blood.
2. The method of claim 1 , wherein said sample is from a human subject with, or suspected of having, asthma.
3. The method of claim 1 , wherein said sample has been treated with a de-glucuronidation agent and/or procedure.
4. The method of claim 3 , wherein said de-glucuronidating agent comprises β-glucuronidase.
5. The method of claim 1 , wherein said testing said sample comprises performing a detection method selected from the group consisting of: mass spectrometry, an immunological assay, HPLC-UV/VIS, LC-Electrochemical detection, or LC-Ampimetric detection method.
6. The method of claim 1 , wherein said sample comprises urine.
7. A method of identifying the presence, severity, risk of, or risk of exacerbation of asthma in a human subject comprising:
testing a sample from a human subject to determine the level of 3-bromotyrosine, wherein said sample has been treated to liberate 3-bromotyrosine from 4-O-glucuronide-3-bromotyrosine, and wherein said sample is selected from the group consisting of: urine, saliva, serum, plasma, tissue biopsy, and whole blood;
b) identifying the presence, severity, risk of, or risk of exacerbation of asthma in said subject based on:
i) an elevated level of 4-O-glucuronide-3-bromotyrosine in said sample compared to a control; and/or
ii) an elevated combined level of 4-O-glucuronide-3-bromotyrosine and 3-bromotyrosine in said sample compared to a control.
8. The method of claim 7 , wherein the presence of asthma is identified in said subject.
9. The method of claim 7 , wherein the severity of asthma is identified in said subject.
10. The method of claim 7 , wherein said subject, prior to step a) is identified as having or being at risk of asthma.
11. The method of claim 7 , further comprising: c) treating said subject with a therapeutic agent used to treat asthma.
12. The method of claim 7 , further comprising: c) generating, transmitting, and/or graphically displaying a report that indicates said 4-O-glucuronide-3-bromotyrosine from said second sample, and/or said combined level of both 4-O-glucuronide-3-bromotyrosine and 3-bromotyrosine from said sample, are elevated compared to corresponding controls, and/or that said subject is in need of a therapeutic agent used to treat asthma.
13. The method of claim 7 , further comprising: c) generating, transmitting, and/or graphically displaying a report that indicates said 4-O-glucuronide-3-bromotyrosine from said sample, and/or said combined level of both 4-O-glucuronide-3-bromotyrosine and 3-bromotyrosine from said sample, are elevated compared to corresponding controls, and/or that said subject has or is at risk of asthma.
14. The method of claim 7 , wherein said sample is from a human subject with, or suspected of having, asthma.
15. The method of claim 7 , wherein said sample has been treated with a de-glucuronidation agent.
16. The method of claim 15 , wherein said de-glucuronidation agent comprises β-glucuronidase.
17. The method of claim 7 , wherein said testing said sample comprises performing a detection method selected from the group consisting of: mass spectrometry, an immunological assay, HPLC-UV/VIS, LC-Electrochemical detection, or LC-Ampimetric detection method.