IP Library Granted Patent US 7,514,229
Granted Patent B2
US 7,514,229 · App. 11/528,890 · Granted Apr 7, 2009

Methods for diagnosing and evaluating treatment of blood disorders

Assignee: The Board of Trustees of the Leland Stanford Junior University
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Quick Facts
Patent No.
US 7,514,229
App. No.
11/528,890
Granted
Apr 7, 2009
Kind
B2
Abstract

Methods, systems and kits are provided for the clinical staging of blood disorders including myelodysplastic syndrome, myeloproliferative diseases and leukemias by differential analysis of hematologic samples for the distribution of one or more hematopoietic stem or progenitor cell subsets. Additional functional, genetic, gene expression, proteomic or other molecular analyses of the hematopoietic stem and progenitor cells from the patients can also be employed in the staging methods of the invention.

Claims (11)

1. A method of staging a blood disorder comprising:

combining a hematologic sample from a patient suspected of having a blood disorder selected from the group consisting of polycythemia vera (PV); chronic myelogenous leukemia (CML); essential thrombocythemia (ET); acute myelogenous leukemia (AML); chronic myelomonocytic leukemia (CMML); post-polycythemic myeloid metaplasia (PPMM); and angiogenic myeloid metaplasia with myelofibrosis (AMM) with specific binding members that are sufficient to distinguish the distribution of hematopoietic stem and progenitor cell subsets between hematopoietic stem cells (HSC); common myeloid progenitors (CMP); megakaryocyte erythroid progenitors (MEP; granulocyte macrophage progenitors (GMP), wherein said binding members include at least one of CD47, IL-3Rα and CD45RA; and

determining the distribution of hematopoietic stem and progenitor cells between said subsets;

wherein the distribution of hematopoietic stem and progenitor cells is indicative of the phenotype of said blood disorder.

2. The method according to claim 1 , wherein said determining step includes flow cytometric analysis.

3. The method according to claim 1 , wherein said specific binding members are antibodies.

4. The method according to claim 3 , wherein said antibodies include specificities for CD34 and CD38.

5. The method according to claim 1 , further comprising antibodies specific for a lineage panel.

6. The method according to claim 1 , further comprising determining a characteristic of at least one of said hematopoietic stem and progenitor cell subsets.

7. The method according to claim 6 , wherein said characteristic is the expression level of at least one gene.

8. The method of claim 7 , wherein said gene encodes a transcription factor.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 23, 2008
From: STANFORD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021879/0186 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2007
From: JAMIESON, CATRIONA HELEN M.; WEISSMAN, IRVING L.
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 019017/0207 →
Continuity (2)
Provisional Application 6072237100 · Sep 29, 2005
Related Publication 20070111238A1 · May 17, 2007