Universal donor stem cells and related methods

US11492591B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11492591-B2
Application numberUS-202117497927-A
CountryUS
Kind codeB2
Filing dateOct 9, 2021
Priority dateMay 8, 2015
Publication dateNov 8, 2022
Grant dateNov 8, 2022

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Disclosed herein are universal donor stem cells and related methods of their use and production. The universal donor stem cells disclosed herein are useful for overcoming the immune rejection in cell-based transplantation therapies. In certain embodiments, the universal donor stem cells disclosed herein do not express one or more MHC-I and MHC-II human leukocyte antigens. Similarly, in certain embodiments, the universal donor stem cells disclosed herein do not express one or more human leukocyte antigens (e.g., HLA-A, HLA-B and/or HLA-C) corresponding to MHC-I and MHC-II human leukocyte antigens, thereby rendering such cells hypoimmunogenic.

First claim

Opening claim text (preview).

What is claimed is: 1. An isolated T cell comprising reduced expression of MHC-I and MHC-II human leukocyte antigens (HLA) relative to a wild-type cell of the same cell type and increased expression of a tolerogenic factor relative to the wild-type cell of the same cell type, wherein the MHC-I human leukocyte antigens are HLA-A, HLA-B, and HLA-C, wherein the MHC-II human leukocyte antigens are HLA-DP, HLA-DQ, and HLA-DR, and wherein the tolerogenic factor is CD47. 2. The isolated T cell of claim 1 , wherein the reduced expression of the MHC-I human leukocyte antigens results from the MHC-I human leukocyte antigens being deleted from at least one allele of the isolated T cell. 3. The isolated T cell of claim 1 , wherein the reduced expression of the MHC-II human leukocyte antigens results from one or more indels being introduced into class II major histocompatibility complex transactivator (CIITA). 4. The isolated T cell of claim 1 , further comprising reduced expression of CIITA. 5. The isolated T cell of claim 1 , wherein the tolerogenic factor is inserted into a safe harbor locus of at least one allele of the isolated T cell. 6. The isolated T cell of claim 5 , wherein the safe harbor locus comprises an AAVS1 locus. 7. The isolated T cell of claim 1 , wherein the tolerogenic factor inhibits immune rejection. 8. The isolated T cell of claim 1 , wherein the isolated T cell does not express HLA-A, HLA-B, and HLA-C. 9. The isolated T cell of claim 1 , wherein the isolated T cell does not express HLA-DP, HLA-DQ, and HLA-DR. 10. The isolated T cell of claim 1 , wherein the isolated T cell does not express CIITA. 11. The isolated T cell of claim 1 , wherein the isolated T cell further comprises an additional tolerogenic factor selected from the group consisting of HLA-G and PD-L1. 12. The T isolated cell of claim 1 , wherein the isolated T cell is a primary T cell. 13. An isolated T cell that does not express HLA-A, HLA-B, HLA-C, HLA-DP, HLA-DQ, and HLA-DR and expresses CD47. 14. The isolated T cell of claim 13 , wherein the isolated T cell is a CIITA indel/indel , HLA-A−, HLA-B −/− , and HLA-C −/− isolated T cell. 15. The isolated T cell of claim 1 , wherein the reduced expression of the MHC-I human leukocyte antigens results from one or more indels being introduced into β-2 microglobulin (B2M). 16. The isolated T cell of claim 1 , further comprising reduced expression of B2M. 17. The isolated T cell of claim 1 , wherein the isolated T cell does not express B2M. 18. The isolated T cell of claim 13 , wherein the isolated T cell is a B2M −/− , CIITA −/− isolated T cell. 19. The isolated T cell of claim 13 , wherein the isolated T cell is a primary T cell.

Assignees

Inventors

Classifications

  • C12N5/0606Primary

    Pluripotent embryonic cells, e.g. embryonic stem cells [ES] (embryonic germ cells C12N5/0611, induced pluripotent stem cells C12N5/0696) · CPC title

  • Cell markers; Cell surface determinants · CPC title

  • A61K39/001Primary

    Preparations to induce tolerance to non-self, e.g. prior to transplantation · CPC title

  • Proteins not provided for elsewhere · CPC title

  • Genetically modified cells · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11492591B2 cover?
Disclosed herein are universal donor stem cells and related methods of their use and production. The universal donor stem cells disclosed herein are useful for overcoming the immune rejection in cell-based transplantation therapies. In certain embodiments, the universal donor stem cells disclosed herein do not express one or more MHC-I and MHC-II human leukocyte antigens. Similarly, in certain …
Who is the assignee on this patent?
Harvard College
What technology area does this patent fall under?
Primary CPC classification C12N5/0606. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 08 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).