Detection of surface-associated human leukocyte elastase
AssigneeRonald Winston
InventorCynthia Bristow
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AssigneeRonald Winston
InventorCynthia Bristow
Estimating the term…
In order to accurately and reliably quantitate HLE on the plasma membranes of the lymphocytes and mononuclear phagocytes, a test sample containing the lymphocytes and mononuclear phagocytes is initially treated with a first antiserum specific for CD4 receptors on the plasma membrane or with a second antiserum specific for chemokine receptors on the plasma membrane. Once the CD4 or chemoline receptors have been rendered non-reactive (competitive) relative to the HLE receptors (also “binding sites”) on the plasma membrane, the test sample is contacted with an immunoreagent specific for interaction with one or more of the HLE receptors on the plasma membranes of the lymphocytes and mononuclear phagocytes. The immunoreagent forms a complex with the HLE binding sites and produces a characteristic physical change in the lymphocytes and mononuclear phagocytes that can be monitored by anyone of a number of standard techniques, (e.g., confocal laser scanning microscopy and flow cytometry).
A method for monitoring the disease progression and pathological phenomena of individuals that experience mylogenous disorders involving leukemia and lymphomas, that correlate with density of Human Leukocyte Elastase (HLE) associated with plasma membranes of lymphocytes and mononuclear phagocytes, said method comprising
The method of claim 6, wherein immunocomplex is monitored by isolation thereof with a solid phase and said reporter or indicator molecule measured immunochromatographic analysis, radial partition immunoassay, or microparticle capture immunoassay.
Dependencies are inferred from the claim text.