IP Library Granted Patent US 11,613,786
Granted Patent B2
US 11,613,786 · App. 16/858,085 · Granted Mar 28, 2023

Clonal haematopoiesis

Inventors: Steven A. McCarroll (Cambridge, MA); Giulio Genovese (Cambridge, MA)
Assignees: President and Fellows of Harvard College; The Broad Institute, Inc.
C12Q1/6886C12Q1/6883C12Q2600/118C12Q2600/156G01N2333/91017
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Quick Facts
Patent No.
US 11,613,786
App. No.
16/858,085
Granted
Mar 28, 2023
Kind
B2
Abstract

The present invention relates to clonal expansion of somatic cells in subjects, and acquired selective advantage of cell clones during the lifetime of a subject. In particular, the invention relates to methods for predicting the development of cancer based on the observation of specific genetic mutations in somatic cell clones, as well as to methods for treating or preventing cancer in a subject, in which clonal expansion of cells comprising specific modifications is observed.

Claims (33)

1. A method of detecting DNMT3A mis-sense mutations in hematopoietic stem cells (HSCs), the method comprising the steps of:

(a) obtaining a blood sample from a human subject

(b) isolating HSCs from the blood sample;

(c) sequencing DNMT3A nucleic acids from one or more of the isolated HSCs;

(d) detecting the presence of a mis-sense mutation in the sequenced DNMT3A nucleic acids, wherein the mis-sense mutation is G543C, F732C, Y735C, R749C, F751C, W753C, or L889C; and

(e) reducing the incidence of HSCs comprising said mutations in the subject and administering to the subject HSCs in which the mutations are absent.

2. The method of claim 1 , wherein the subject is at least 50 years of age.

3. The method of claim 1 , wherein the subject is or has been exposed to a human carcinogen in sufficient amount and/or frequency for such carcinogen to be a potential cause of hematological malignancy.

4. The method of claim 3 , wherein the carcinogen comprises a tobacco product, an organic solvent, a virus, a compound found in grilled red meat, ionizing radiation, a heavy metal or compound thereof, or any combination thereof.

5. The method of claim 1 , wherein the HSCs in which the mutations are absent are administered in a bone marrow transplantation.

6. The method of claim 1 , wherein the HSCs in which the mutations are absent are administered in a blood transfusion.

7. A method of determining whether a subject is predisposed to a hematological malignancy, the method comprising the steps of:

(a) obtaining a blood sample from a human subject

(b) isolating hematopoietic stem cells (HSCs) from the blood sample;

(c) sequencing DNMT3A nucleic acids from one or more of the isolated HSCs;

(d) detecting the presence of a mis-sense mutation in the sequenced DNMT3A nucleic acids, wherein the mis-sense mutation is G543C, F732C, Y735C, R749C, F751C, W753C, or L889C;

(e) determining that the subject is predisposed to a hematological malignancy if the mis-sense mutation is detected; and

(f) reducing the incidence of HSCs comprising said mutations in the subject and administering to the subject HSCs in which the mutations are absent.

8. The method of claim 7 , wherein the hematological malignancy is a myeloproliferative neoplasm, a myelodysplastic syndrome, acute myeloid leukemia or chronic lymphocytic leukemia.

9. The method of claim 7 , wherein the human subject is at least 50 years of age.

10. The method of claim 7 , wherein the human subject has been exposed to a human carcinogen in sufficient amount and/or frequency for such carcinogen to be a potential cause of hematological malignancy.

11. The method of claim 10 , wherein the carcinogen comprises a tobacco product, an organic solvent, a virus, a compound found in grilled red meat, ionizing radiation, a heavy metal or compound thereof, or any combination thereof.

12. The method of claim 7 , wherein the HSCs in which the mutations are absent are administered in a bone marrow transplantation.

13. The method of claim 7 , wherein the HSCs in which the mutations are absent are administered in a blood transfusion.

14. A method of selecting hematopoietic cells for transplantation, the method comprising the steps of:

(a) obtaining a sample comprising hematopoietic cells from a human subject;

(b) sequencing DNMT3A nucleic acids from one or more of the hematopoietic cells;

(c) detecting the absence of G543C, F732C, Y735C, R749C, F751C, W753C, and L889C mis-sense mutations in the sequenced DNMT3A nucleic acids; and

(d) collecting the remaining hematopoietic cells in the sample for transplantation.

15. The method of claim 14 , wherein the hematopoietic cells are collected for autologous transplantation.

16. The method of claim 14 , wherein the hematopoietic cells are collected for allogenic transplantation.

17. The method of claim 14 , wherein the sample is obtained from the human subject prior to diagnosis of a hematological malignancy.

18. The method of 14 , wherein the sample is derived from cord blood.

Assignments (3)
LICENSE Recorded Mar 21, 2025
From: BROAD INSTITUTE, INC.
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 070589/0127 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2020
From: MCCARROLL, STEVEN ANDREW
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 053038/0685 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2020
From: GENOVESE, GIULIO
To: THE BROAD INSTITUTE, INC.
Reel/Frame 053038/0689 →
Continuity (3)
Continuation 15528807
Provisional Application 62084112 · Nov 25, 2014
Related Publication 20210123105A1 · Apr 29, 2021
Cited By (1)
US 12,503,733