Identification and uses of vasculature forming progenitor cells and progenitor cell combinations

US11369641B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11369641-B2
Application numberUS-201716323079-A
CountryUS
Kind codeB2
Filing dateAug 25, 2017
Priority dateAug 26, 2016
Publication dateJun 28, 2022
Grant dateJun 28, 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.

Methods, compositions, and kits for producing functional blood vessels, and progenitors thereof are provided. Human disorders of the vascular system are treated by reconstitution of functional vessels in vivo through co-transplantation with supporting niche stromal cells for treatment of ischemic injury in the peripheral limbs and heart. The cell populations of the invention, when engrafted into a recipient, anastomose with host vasculature and regenerate functional blood vessels.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for generating functional blood vessels in a human individual recipient, the method comprising: a) isolating P1 and P2 cells from human adipose stromal tissue, wherein P1 cells are defined as CD45 − Tie2 + CD105 + PDGFRα − CD31 + and P2 cells are defined as CD45 − Tie2 + CD105 + PDGFRα + CD31 − ; and b) administering to the human individual recipient a composition comprising an effective dose of the isolated P1 and P2 cells of step (a), at a site where regeneration of vessels is desired, wherein the isolated P1 and P2 cells are present in the composition at a ratio of 1:100 to 100:1, and wherein the isolated P1 and P2 cells are autologous with respect to the human individual recipient. 2. The method of claim 1 , wherein the effective dose is from 10 3 to 10 10 total cells. 3. The method of claim 1 , wherein the composition is provided in a matrix. 4. A method for generating functional blood vessels in a human individual recipient, the method comprising: a) isolating P1 and P2 cells from human adipose stromal tissue, wherein P1 cells are defined as CD45 − Tie2 + CD105 + PDGFRα − CD31 + and P2 cells are defined as CD45 − Tier CD105 + PDGFRα + CD31 − ; and b) administering to the human individual recipient a composition comprising an effective dose of the isolated P1 and P2 cells of step (a), at a site where regeneration of vessels is desired, wherein the isolated P1 and P2 cells are present in the composition at a ratio of 1:100 to 100:1, and wherein the isolated P1 and P2 cells are allogeneic with respect to the human individual recipient. 5. The method of claim 1 , wherein the P1 and P2 cells are freshly isolated from lipoaspirate. 6. The method of claim 1 , wherein the P1 and P2 cells are isolated from adult human adipose stromal tissue. 7. The method of claim 1 , wherein the human individual recipient suffers from ischemic cardiovascular disease. 8. The method of 7 , wherein the human individual recipient suffers from coronary artery disease (CAD), peripheral arterial disease (PAD), or stroke. 9. A method for generating adipose tissue in a human individual recipient, the method comprising: a) isolating P2 cells from human adipose stromal tissue, wherein P2 cells are defined as CD45 − Tier CD105 + PDGFRα + CD31 − ; and b) administering to the human individual recipient a composition comprising an effective dose of the isolated P2 cells of step (a), at a site where regeneration of adipose tissue is desired, wherein the isolated P2 cells are autologous with respect to the human individual recipient, wherein the composition lacks P1 cells, and wherein P1 cells are defined as CD45 − Tie2 + CD105 + PDGFRα 31 CD31 + .

Assignees

Inventors

Classifications

  • A61K35/28Primary

    Bone marrow; Haematopoietic stem cells; Mesenchymal stem cells of any origin, e.g. adipose-derived stem cells · CPC title

  • A61K35/35Primary

    Fat tissue; Adipocytes; Stromal cells; Connective tissues (adipose-derived stem cells A61K35/28; collagen A61K38/39) · CPC title

  • for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

  • Adipose-derived stem cells [ADSC]; Adipose stromal stem cells · CPC title

  • Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · 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 US11369641B2 cover?
Methods, compositions, and kits for producing functional blood vessels, and progenitors thereof are provided. Human disorders of the vascular system are treated by reconstitution of functional vessels in vivo through co-transplantation with supporting niche stromal cells for treatment of ischemic injury in the peripheral limbs and heart. The cell populations of the invention, when engrafted int…
Who is the assignee on this patent?
Univ Leland Stanford Junior
What technology area does this patent fall under?
Primary CPC classification A61K35/28. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jun 28 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).