US2023226153A1PendingUtilityA1
Stem cells for transplantation and manufacturing method therefor
Assignee: NAT CENTER NEUROLOGY & PSYCHIATRYPriority: May 22, 2013Filed: Jan 30, 2023Published: Jul 20, 2023
Est. expiryMay 22, 2033(~6.8 yrs left)· nominal 20-yr term from priority
A61K 38/2066C12N 5/0663A61L 27/3834A61K 35/28C07K 14/5428C12N 5/0662C12N 7/00C12N 15/86C12N 2501/231C12N 2510/02A61K 48/00A61P 37/06A61K 39/001A61K 2039/577A61K 2039/552A61P 1/16A61P 19/04A61P 21/00A61P 25/00A61P 9/00C12N 2510/00C12N 2750/14143C12N 2750/14171
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Claims
Abstract
It is intended to provide MSCs for transplantation that have an improved post-transplantation cell survival rate and engraftment rate and are highly safe with fewer adverse reactions, and a method for conveniently producing MSCs for transplantation having a high cell survival rate and engraftment rate. As means therefor, the present invention provides a stem cell for transplantation comprising an MSC capable of overexpressing IL-10.
Claims
exact text as granted — not AI-modified1 - 11 . (canceled)
12 . A composition comprising human mesenchymal stem cells (hMSCs) and a viral immunogen, wherein, when the composition is administered to a subject, it suppresses the subject's immune response to the viral immunogen.
13 . The composition according to claim 12 , wherein the viral immunogen is from an adenovirus, adeno-associated virus (AAV), retrovirus, or lentivirus.
14 . The composition according to claim 13 , wherein the viral immunogen is from an AAV or adenovirus.
15 . The composition according to claim 12 , wherein the viral immunogen is a recombinant viral immunogen.
16 . The composition according to claim 15 , wherein the recombinant viral immunogen is a recombinant virus for expression of IL-10.
17 . The composition according to claim 12 , wherein the composition induces tolerance to the viral immunogen when administered to the subject.
18 . The composition according to claim 12 , wherein the hMSCs are recombinant hMSCs.
19 . The composition according to claim 18 , wherein the recombinant hMSCs overexpress exogenous IL-10.
20 . The composition according to claim 12 , further comprising recombinant IL-10.
21 . A method for reducing an immune response to a viral immunogen in a subject in need thereof, the method comprising:
administering to the subject: (i) human mesenchymal stem cells (hMSCs); and (ii) the viral immunogen, whereby the immune response to the viral immunogen is suppressed.
22 . The method according to claim 21 , wherein the viral immunogen is from an adenovirus, adeno-associated virus (AAV), retrovirus, or lentivirus.
23 . The method according to claim 21 , wherein the viral immunogen is a recombinant viral immunogen.
24 . The method according to claim 23 , wherein the recombinant viral immunogen is a recombinant virus for expression of IL-10.
25 . The method according to claim 22 , wherein the viral immunogen is from an AAV or adenovirus.
26 . The method according to claim 21 , wherein suppression of the immune response comprises induction of tolerance to the viral immunogen.
27 . The method according to claim 21 , wherein the hMSCs are recombinant hMSCs.
28 . The method according to claim 27 , wherein the recombinant hMSCs overexpress exogenous IL-10.
29 . The method according to claim 21 , wherein the hMSCs and the viral immunogen are co-administered at the same time.
30 . The method according to claim 21 , wherein the hMSCs and the viral immunogen are administered sequentially.
31 . The method according to claim 21 , further comprising administering recombinant IL-10.Join the waitlist — get patent alerts
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