US2006134706A1PendingUtilityA1
Atopic dermatitis inducer
Est. expiryJul 9, 2023(expired)· nominal 20-yr term from priority
A61P 37/08A61P 17/00C07K 16/4291A61K 2039/505C07K 14/47C07K 16/18C07K 16/42
46
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Claims
Abstract
An atopic dermatitis inducer binding to a human own IgE antibody and activating mast cells and basophiles, which includes a purified human secretion fraction, or an antigenic molecule or an antigenic determinant in the purified fraction, and obtained through the following steps of: filtering a human secretion, removing insoluble matters and collecting the filtrate; mixing the filtrate with a ConA-affinity carrier and collecting the supernatant; and separating a component having a histamine-releasing activity from the supernatant by column chromatography. This inducer is effective in diagnosing and treating human atopic dermatitis.
Claims
exact text as granted — not AI-modified1 - 8 . (canceled)
9 . A composition activating mast cells and basophils upon binding to a human own IgE antibody and having an atopic dermatitis inducing activity, which is obtained from a human secretion through the following steps of:
filtering a human secretion, removing insoluble matters and collecting the filtrate; mixing the filtrate with a ConA-affinity carrier and collecting the supernatant; and separating a component having an histamine-releasing activity from the supernatant by column chromatography.
10 . The composition of claim 9 , wherein the column chromatography is anion exchange column chromatography and/or reverse phase column chromatography.
11 . An antibody prepared by using the composition of claim 9 as an antigen, and specifically binding to the composition of claim 9 .
12 . An antibody prepared by using the composition of claim 10 as an antigen, and specifically binding to the composition of claim 10 .
13 . A method of diagnosing atopic dermatitis, which comprises testing whether or not an IgE antibody binding to the composition of claim 9 exists in the serum of a subject and determining that the subject whose serum contains the IgE antibody is a patient with atopic dermatitis or a high-risk individual for atopic dermatitis.
14 . A method of diagnosing atopic dermatitis, which comprises testing whether or not an IgE antibody binding to the composition of claim 10 exists in the serum of a subject and determining that the subject whose serum contains the IgE antibody is a patient with atopic dermatitis or a high-risk individual for atopic dermatitis.
15 . A method of diagnosing atopic dermatitis, which comprises adding the composition of claim 9 to a leukocyte fraction collected from the blood of a subject, and determining that the subject is a patient with atopic dermatitis or a high-risk individual for atopic dermatitis from the degree of histamine release in the leukocyte fraction.
16 . A method of diagnosing atopic dermatitis, which comprises adding the composition of claim 10 to a leukocyte fraction collected from the blood of a subject, and determining that the subject is a patient with atopic dermatitis or a high-risk individual for atopic dermatitis from the degree of histamine release in the leukocyte fraction.
17 . A method of diagnosing atopic dermatitis, which comprises testing whether or not a substance binding to an antibody of claim 11 exists in a biological sample of a subject, and determining that the subject whose sample contains the substance is a patient with atopic dermatitis or a high-risk individual for atopic dermatitis.
18 . A reagent for determining a high-risk individual for atopic dermatitis, which comprises a patch test material having the composition of claim 9 .
19 . A reagent for determining a high-risk individual for atopic dermatitis, which comprises a patch test material having the composition of claim 10 .
20 . A drug for desensitization therapy of atopic dermatitis, which contains the composition of claim 9 as an active ingredient.
21 . A drug for desensitization therapy of atopic dermatitis, which contains the composition of claim 10 as an active ingredient.
22 . A kit for diagnosing atopic dermatitis, which contains the composition of claim 9 as an active ingredient.
23 . A kit for diagnosing atopic dermatitis, which contains the composition of claim 10 as an active ingredient.
24 . A method of preparing a composition, which is derived from a human secretion, activates mast cells and basophils upon binding to a human own IgE antibody, and has an atopic dermatitis inducing activity, comprising the following steps of:
filtering a human secretion, removing insoluble matters and collecting the filtrate; mixing the filtrate with a ConA-affinity carrier and collecting the supernatant; and separating a component having an histamine-releasing activity from the supernatant by column chromatography.Cited by (0)
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