IP Library Granted Patent US 10,960,071
Granted Patent B2
US 10,960,071 · App. 16/902,420 · Granted Mar 30, 2021

Platform for generating safe cell therapeutics

Inventors: Richard Klemke (La Jolla, CA); Huawei Wang (San Diego, CA)
Assignee: The Regents of the University of California
A61K39/215A61K35/12A61K39/001102A61K2039/515A61K2039/545
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Quick Facts
Patent No.
US 10,960,071
App. No.
16/902,420
Granted
Mar 30, 2021
Kind
B2
Abstract

Provided herein are cytoplasts, compositions comprising cytoplasts, methods of using cytoplasts, and methods of treating a subject, such as providing benefits to a healthy or unhealthy subject, or treating or diagnosing a disease or condition in a subject. In some embodiments, methods of treating a subject include: administering to the subject a therapeutically effective amount of a composition comprising a cytoplast. Also, provided herein are compositions (e.g., pharmaceutical compositions) that include a cytoplast. Also, provided herein are kits comprising instructions for using the compositions or methods.

Claims (17)

1. A cell without a nucleus, the cell comprising: a homing receptor that is specific to a ligand expressed on one or more cells in lymph tissue and one or more intracellular organelles for synthesis or secretion of a vaccine composition in an absence of the nucleus.

2. The cell of claim 1 , wherein the cell is not a red blood cell.

3. The cell of claim 1 , wherein the cell without the nucleus is derived from a nucleated parent cell to which the one or more intracellular organelles is endogenous.

4. The cell of claim 1 , wherein the vaccine composition is against a coronavirus or an influenza virus.

5. The cell of claim 4 , wherein the coronavirus is a Severe Acute Respiratory Syndrome coronavirus.

6. The cell of claim 1 , wherein the vaccine composition is a RNA, or an antigenic peptide or protein, or a combination thereof.

7. The cell of claim 1 , wherein the vaccine composition is secretory.

8. The cell of claim 1 , wherein the homing receptor comprises C—X—C chemokine receptor type 3.

9. The cell of claim 1 , wherein the homing receptor comprises CD44 antigen.

10. The cell of claim 1 , wherein the homing receptor comprises C—C chemokine receptor type 7.

11. The cell of claim 1 , wherein the cell has a diameter that is between about 1 micrometer (μm) to about 100 μm.

12. The cell of claim 1 , wherein the cell is viable for at least 24 hours following removal from cryohibernation or cryopreservation.

13. The cell of claim 1 , that is cryopreserved or cryohybernated.

14. The cell of claim 1 , wherein the synthesis or the secretion of the vaccine composition in the absence of the nucleus is performed by the cell for greater than or equal to about 3 days.

15. The cell of claim 1 , wherein the cell is in a pharmaceutically acceptable carrier.

16. The cell of claim 1 , wherein the cell is isolated and purified.

17. A population of cells comprising a plurality of the cell of claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2020
From: KLEMKE, RICHARD; WANG, HUAWEI
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 053014/0009 →
Continuity (3)
Continuation 16636249
Provisional Application 62542133 · Aug 7, 2017
Related Publication 20200306366A1 · Oct 1, 2020
Cited By (3)
US 12,264,336 US 12,467,037 US 12,559,723