IP Library Granted Patent US 9,255,926
Granted Patent B2
US 9,255,926 · App. 12/297,389 · Granted Feb 9, 2016

Hematopoietic cell phenotyping using circulating cell-free markers

Inventor: Maher Albitar (Coto De Caza, CA)
Assignee: QUEST DIAGNOSTICS INVESTMENTS INCORPORATED
G01N33/57426G01N33/57488G01N33/6869G01N2333/70596G01N2800/56
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Quick Facts
Patent No.
US 9,255,926
App. No.
12/297,389
Granted
Feb 9, 2016
Kind
B2
Abstract

The present invention provides methods of classifying cluster of differentiation (CD) marker phenotype for hematopoietic cancer cells using multiple circulating cell-free CD markers in bodily fluid. In other aspects, treatment and disease progression of particular hematopoietic cancers can be monitored by measuring the levels of CD and other markers i bodily fluids of a patient.

Claims (9)

1. A method for predicting survival or remission duration in a patient with myelodysplastic syndrome (MDS), the method comprising:

(a) assaying a blood plasma sample from a patient diagnosed as having MDS to determine the level of circulating cell-free CD4 marker in said sample, wherein assaying comprises contacting the blood plasma sample with an antibody specific for CD4,

(b) correlating the level of circulating cell-free CD4 marker determined in step (a) with the patient's predicted survival or remission duration, and

(c) identifying the patient as

(i) having a longer predicted survival or remission duration if the level of cell-free CD4 is determined to be greater than 1029 U/μl, whereby a level greater than 1029 U/μl indicates that the patient will have a longer predicted survival or remission duration than is indicated by a level less than 1029 U/μl; or

(ii) having a shorter predicted survival or remission duration if the level of cell-free CD4 is determined to be less than 1029 U/μl, whereby a level less than 1029 U/μl indicates that the patient will have a shorter survival or remission duration than is indicated by a level greater than 1029 U/μl.

2. The method of claim 1 wherein the antibody has a detectable label.

3. The method of claim 2 wherein the label is selected from the group consisting of a radioisotope, an enzyme, an enzyme substrate, a luminescent substance, a fluorescent substance, biotin, and a colored substance.

4. The method of claim 1 wherein assaying comprises performing a process selected from the group consisting of a sandwich immunoassay, a radioimmunoassay, immunoprecipitation, Western blotting, and an enzyme-linked immunosorbent assay.

Assignments (2)
ENTITY CONVERSION Recorded Nov 14, 2018
From: QUEST DIAGNOSTICS INVESTMENTS INCORPORATED
To: QUEST DIAGNOSTICS INVESTMENTS LLC
Reel/Frame 047532/0890 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2009
From: ALBITAR, MAHER
To: QUEST DIAGNOSTICS INVESTMENTS INCORPORATED
Reel/Frame 023343/0956 →
Continuity (2)
Continuation In Part 11206260 · Aug 17, 2005
Related Publication 20100028930A1 · Feb 4, 2010