US2006188500A1PendingUtilityA1
Methods of predicting therpeutic response in atopic dermatitis to IL-31 antagonists
Individually held — no corporate assignee on recordPriority: Feb 14, 2005Filed: Feb 14, 2006Published: Aug 24, 2006
Est. expiryFeb 14, 2025(expired)· nominal 20-yr term from priority
A61P 43/00A61P 31/22A61P 37/04A61P 35/00A61P 37/08A61P 17/14A61P 17/04A61K 2039/505C07K 2317/76A61K 49/0008G01N 33/6869G01N 33/505A61P 17/10C07K 16/244C07K 16/2803G01N 33/6881C07K 14/52A61P 17/00A61K 49/006A61P 17/02A61K 2039/545A61K 39/3955
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Claims
Abstract
The present invention relates to predicting therapeutic response of treating patients suffering from itching and puritis mediated by cutaneous lymphocyte antigen positive T cells in atopic dermatitis. The invention also includes methods of predicting a therapeutically responsive patient population.
Claims
exact text as granted — not AI-modified1 . A method of treating atopic dermatits skin comprising administering an antagonist molecule to a mammal with the atopic dermatitis skin wherein the skin is characterized by cutaneous lymphocyte antigen positive T cells and the antagonist molecule specifically binds to the polypeptide comprising the amino acid sequence as shown in SEQ ID NO:2 or SEQ ID NO: 4, and whereby administration of the antagonist molecule improves, prevents, inhibits or reduces the diseased skin.
2 . The method according to claim 1 , wherein the mammal is a human.
3 . The method according to claim 2 , wherein the antagonist is an antibody or antibody fragment.
4 . The method according to claim 3 , wherin the antagonist molecule specifically binds to the polypeptide comprising the amino acid sequence as shown in SEQ ID NO:2.
5 . The method according to claim 1 , wherein the atopic dermatitis skin is pruritic.
6 . A method for treating pruritis from atopic dermatitis comprising administering an antagonist molecule to a mammal with the pruritis wherein the pruritis is characterized by cutaneous lymphocyte antigen positive T cells and wherein the antagonist molecule specifically binds to the polypeptide having the amino acid sequence as shown in SEQ ID NO:2 or in SEQ ID NO: 4, and whereby administration of the antagonist molecule improves, prevents, inhibits or reduces the pruritis.
7 . The method according to claim 6 , wherein the mammal is a human.
8 . The method according to claim 6 , wherein the antagonist is an antibody or antibody fragment.
9 . The method according to claim 8 , wherin the antagonist molecule specifically binds to the polypeptide comprising the amino acid sequence as shown in SEQ ID NO:2.
10 . A method for predicting therapeutic response to an IL-31 antagonist in an individual with atopic dermatitis in need of IL-31 antagonist therapy comprising obtaining a biological sample from the patient, isolating circulating cutaneous lymphocyte positive T cells from the biological sample, and detecting IL-31 production from the isolated cutaneous lymphocyte positive T cells.
11 . The method according to claim 10 , wherein the IL-31 is detected by specifically binding to an IL-31 antagonist.
12 . The method according to claim 11 , wherein the IL-31 antagonist is an anti-IL-31 antibody or antibody fragment.
13 . The method according to claim 12 , wherin the antagonist molecule specifically binds to the polypeptide comprising the amino acid sequence as shown in SEQ ID NO:2.
14 . The method according to claim 10 , comprising the additional step of stimulating or activating the cutaneous lymphocyte antigen positive T cells.
15 . The method according to claim 14 , wherein the IL-31 is detected by specifically binding to an IL-31 antagonist.
16 . The method according to claim 15 , wherein the IL-31 antagonist molecule is an anti-IL-31 antibody or antibody fragment.
17 . The method according to claim 16 , wherin the antagonist molecule specifically binds to the polypeptide comprising the amino acid sequence as shown in SEQ ID NO:2.Join the waitlist — get patent alerts
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