US2021324339A1PendingUtilityA1
Cell-derived particles presenting heterologous cd24 and use thereof in therapy
Est. expiryApr 16, 2040(~13.8 yrs left)· nominal 20-yr term from priority
C12N 2501/599C12N 2500/90C12N 5/0656A61K 35/407C12N 2510/00C12N 5/0686A61K 35/33A61P 37/02A61K 9/5068C07K 14/70596C12N 2501/33C12N 2501/998C07K 14/71
56
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
A method of producing cell derived particles is disclosed. The method comprising isolating cell-derived particles from a biological sample comprising cells modified to present CD24 so as to obtain a preparation of the cell-derived particles substantially devoid of intact cells. Cell derived particles, a culture medium and a cell culture are also disclosed.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of producing cell derived particles, the method comprising isolating cell-derived particles from a biological sample comprising cells modified to present CD24 so as to obtain a preparation of the cell-derived particles substantially devoid of intact cells.
2 . The method of claim 1 , further comprising modifying cells to present CD24 to obtain said cells modified to present CD24 prior to said isolating cell-derived particles from a biological sample.
3 . The method of claim 2 , further comprising culturing the cells modified to present CD24 prior to said isolating cell-derived particles from a biological sample.
4 . The method of claim 1 , wherein the cells are cultured in a serum-free culture medium.
5 . The method of claim 4 , wherein said culture medium comprises Expi medium.
6 . The method of claim 1 , wherein the cells are cultured in a suspension culture.
7 . The method of claim 6 , wherein the suspension culture is in the absence of insulin and albumin.
8 . The method of claim 1 , wherein the cells are cultured in a 2D culture.
9 . The method of claim 8 , wherein said 2D culture comprises insulin and albumin.
10 . The method of claim 1 , wherein said preparation of the cell-derived particles comprises about 1×10 10 -1×10 15 cell derived particles per liter.
11 . The method of claim 6 , wherein when said cells are cultured in a suspension culture, said preparation of the cell-derived particles comprises at least about 3 times more cell derived particles as compared to cells cultured in a 2D culture.
12 . A culture medium comprising Expi medium, insulin and albumin.
13 . A cell culture comprising cells and the medium of claim 12 .
14 . Cell-derived particles presenting heterologous CD24 produced according to the method of claim 1 .
15 . The method of claim 1 , wherein said CD24 is as set forth in SEQ ID NO: 9 or encodable by SEQ ID NO: 8.
16 . The method of claim 1 , wherein said cell-derived particles are selected from the group consisting of exosomes, ARMM, microvesicles, exomeres, membrane particles, membrane vesicles and ectosomes.
17 . The method of claim 1 , wherein said cell-derived particles have a mean particle diameter of about 80 to about 220 nm.
18 . The method of claim 1 , wherein said cell-derived particles are exosomes.
19 . The method of claim 1 , wherein said cells are cells of an animal or a human tissue.
20 . The method of claim 1 , wherein said cells are healthy cells.
21 . The method of claim 1 , wherein said cells are genetically modified cells.
22 . The method of claim 1 , wherein said cells are fibroblast cells or kidney cells.
23 . The method of claim 1 , wherein said cells are HEK-293 cells.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.