IP Library Granted Patent US 8,969,315
Granted Patent B2
US 8,969,315 · App. 13/340,589 · Granted Mar 3, 2015

Enhancement of placental stem cell potency using modulatory RNA molecules

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Quick Facts
Patent No.
US 8,969,315
App. No.
13/340,589
Granted
Mar 3, 2015
Kind
B2
Abstract

Provided herein are methods of producing enhanced placental stem cells by modulatory RNA molecules. Also provided herein are methods of using enhanced placental stem cells, for example, to treat individuals having a disease, disorder or condition caused by, or relating to, an unwanted or harmful immune response. Further provided herein are compositions comprising said enhanced placental stem cells.

Claims (12)

1. A method of treating an individual having or at risk of developing a disease, disorder or condition having an inflammatory component, comprising administering to the individual a therapeutically effective amount of enhanced placental stem cells,

wherein said enhanced placental stem cells comprise or have been contacted with an effective amount of modulatory RNA molecules that decrease expression of one or more human nuclear receptors in said enhanced placental stem cells, resulting in suppression of soluble IL-23 protein produced by peripheral blood mononuclear cells (PBMCs) in the presence of said enhanced placental stem cells compared to placental stem cells not contacted with said modulatory RNA molecules,

wherein said modulatory RNA molecules are small interfering RNAs (siRNAs), microRNA inhibitors (miR inhibitors), or micro RNA mimics (miR mimics),

wherein said one or more human nuclear receptors is selected from the group consisting of: vitamin D receptor (VDR); nuclear receptor subfamily 4, group A, member 3 (NR4A3); nuclear receptor subfamily 0, group B, member 2 (NR0B2); nuclear receptor subfamily 1, group 1, member 2 (NR1I2); nuclear receptor subfamily 1, group H, member 3 (NR1H3); and deoxynucleotidyltransferase, terminal, interacting protein 1 (DNTTIP1), and

wherein the therapeutically effective amount is an amount sufficient to cause a detectable improvement in one or more symptoms of said disease, disorder or condition.

2. The method of claim 1 , wherein said modulatory RNA molecules are siRNAs.

3. The method of claim 1 , wherein said modulatory RNA molecules are selected from a library.

4. The method of claim 3 , wherein said library is a human nuclear receptor library, human phosphatase siRNA library, or an anti-miR library.

5. The method of claim 1 , wherein said placental stem cells are CD10 − , CD34 − , CD105 + , CD200 + placental stem cells.

6. The method of claim 1 , wherein said placental stem cells express CD200 and do not express HLA-G, or express CD73, CD105, and CD200, or express CD200 and OCT-4, or express CD73 and CD105 and do not express HLA-G.

7. The method of claim 5 , wherein said placental stem cells are additionally CD90 + and CD45 − .

8. The method of claim 5 , wherein said placental stem cells are additionally CD80 − and CD86 − .

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2025
From: CELULARITY INC.
To: CELENIV PTE. LTD.
Reel/Frame 073705/0109 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2017
From: CLARITY ACQUISITION II LLC
To: CELULARITY, INC.
Reel/Frame 044780/0261 →
MERGER Recorded Nov 8, 2017
From: ANTHROGENESIS CORPORATION
To: CLARITY ACQUISITION II LLC
Reel/Frame 044413/0680 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2015
From: ABBOT, STEWART; KARASIEWICZ-MENDEZ, KATHY E.; VOSKINARIAN-BERSE, VANESSA; ZHANG, XIAOKUI
To: ANTHROGENESIS CORPORATION
Reel/Frame 034712/0710 →