US2016208011A1PendingUtilityA1
Ccr3 modulation in the treatment of aging-associated impairments, and compositions for practicing the same
Assignee: UNIV LELAND STANFORD JUNIORPriority: Jan 28, 2010Filed: Jan 8, 2016Published: Jul 21, 2016
Est. expiryJan 28, 2030(~3.5 yrs left)· nominal 20-yr term from priority
C07K 16/24C12Y 207/10001C12N 15/1138C12N 15/1136A61K 2039/505A61K 38/19C07K 16/2896C07K 2317/76A61K 38/45C12N 2310/14C12Q 2600/136A61K 31/7088C12N 2799/06C12N 2799/022C12Q 2600/158A61K 31/00C07K 16/28C12Q 1/6883
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Claims
Abstract
Methods of treating an adult mammal for an aging-associated impairment are provided. Aspects of the methods include modulating CCR3, e.g., by modulating eotaxin-1/CCR3 interaction, in the mammal in a manner sufficient to treat the mammal for the aging-associated impairment. A variety of aging-associated impairments may be treated by practice of the methods, which impairments include cognitive impairments.
Claims
exact text as granted — not AI-modified1 . A method of treating an adult mammal for an aging-associated impairment, the method comprising:
modulating CCR3 in the mammal in a manner sufficient to treat the adult mammal for the aging-associated impairment.
2 . The method according to claim 1 , wherein modulating CCR3 comprising modulating eotaxin-1/CCR3 interaction.
3 . The method according to claim 2 , wherein eotaxin-1/CCR3 interaction is modulated by reducing active systemic eotaxin-1 in the mammal.
4 . The method according to claim 3 , wherein the active systemic eotaxin-1 is reduced in the mammal by administering to the mammal an effective amount of an active systemic eotaxin-1 reducing agent.
5 . The method according to claim 4 , wherein the active systemic eotaxin-1 reducing agent is an eotaxin-1 binding agent.
6 . The method according to claim 5 , wherein the eotaxin-1 binding agent comprises an antibody or binding fragment thereof.
7 . The method according to claim 5 , wherein the eotaxin-1 binding agent comprises a small molecule.
8 . The method according to claim 4 , wherein the active systemic eotaxin-1 reducing agent comprises an eotaxin-1 expression inhibitory agent.
9 . The method according to claim 8 , wherein the eotaxin-1 expression inhibitory agent comprises a nucleic acid.
10 . The method according to claim 1 , wherein eotaxin-1/CCR3 interaction is modulated by reducing CCR3 activity in the mammal.
11 . The method according to claim 10 , wherein the CCR3 activity is reduced in the mammal by administering to the mammal an effective amount of an active CCR3 reducing agent.
12 . The method according to claim 11 , wherein the active CCR3 reducing agent is a CCR3 binding agent.
13 . The method according to claim 12 , wherein the CCR3 binding agent comprises an antibody or binding fragment thereof.
14 . The method according to claim 12 , wherein the CCR3 binding agent comprises a small molecule.
15 . The method according to claim 11 , wherein the active CCR3 reducing agent comprises a CCR3 expression inhibitory agent.
16 . The method according to claim 15 , wherein the CCR3 expression inhibitory agent comprises a nucleic acid.
17 . The method according to claim 1 , wherein the mammal is a primate.
18 . The method according to claim 17 , wherein the primate is a human.
19 . The method according to claim 1 , wherein the adult mammal is an elderly mammal.
20 . The method according to claim 19 , wherein the elderly mammal is a human that is 60 years or older.
21 . The method according to claim 1 , wherein the aging-associated impairment comprises a cognitive impairment.
22 . The method according to claim 1 , wherein the adult mammal suffers from an aging associated disease condition.
23 . The method according to claim 1 , wherein the aging associated disease condition is a cognitive decline disease condition.Join the waitlist — get patent alerts
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