US2018311328A1PendingUtilityA1
Peptide Selection Method
Assignee: APITOPE TECH BRISTOL LIMITEDPriority: Aug 21, 2000Filed: Mar 20, 2018Published: Nov 1, 2018
Est. expiryAug 21, 2020(expired)· nominal 20-yr term from priority
A61P 37/00A61P 37/08A61P 37/06A61P 37/02A61K 38/10G01N 33/505C07K 14/4713A61K 39/0008A61K 38/17C07K 14/47A61P 25/00C07K 7/00
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Claims
Abstract
There is provided a method for selecting a tolerogenic peptide by selecting a peptide which is capable of binding to an MHC class I or H molecule without further processing. There is also provided a peptide selected by such a method and its use in a pharmaceutical composition and a method to treat and/or prevent a disease.
Claims
exact text as granted — not AI-modified1 . A method for selecting a tolerogenic peptide which comprises the step of selecting a peptide which is capable of binding to an MHC class I or II molecule without further processing.
2 . A method according to claim 1 , wherein the peptide is capable of binding to an MHC class II molecule without further processing.
3 . A method according to claim 1 , wherein the peptide is selected from a plurality of peptides each comprising a T cell epitope.
4 . A method according to claim 3 , wherein the plurality of peptides is eluted from the MHC class II molecules of an antigen presenting cell.
5 . A method according to claim 3 , wherein each peptide in the plurality of peptides is capable of inducing a disease associated with the antigen in a subject when administered to the subject with adjuvant.
6 . A method according to claim 1 , wherein the peptide is selected from a nested set of truncated peptides.
7 . A method claim 1 , wherein the peptide comprises a T cell epitope and presence of a T cell epitope is determined by:
(i) treating: a sample of cells from a subject having the disease, and a sample of cells from a subject not having the disease with the peptide; and (ii) comprising the T cell responses between the cell samples.
8 . A method according to claim 1 which comprises the following steps:
(i) treating an antigen processing independent presentation system (APIPS) with a peptide; and
(ii) analyzing binding of the peptide to MHC class I or II molecules within the APIPS.
9 . A method according to claim 8 , wherein binding of the peptide to MHC class I or II molecules is analysed by adding T cells and measuring T cell activation.
10 . A method according to claim 8 , wherein the APIPS comprises:
(i) fixed antigen presenting cells (ii) lipid membranes comprising MHC class I or II molecules; or (iii) plate-bound MHC class I or II molecules.
11 . A peptide selected by the method according to claim 1 .
12 . A peptide according to claim 11 , which is selected from the following myelin basic protein peptides: 30-44, 80-94, 83-99, 81-95, 82-96, 83-97, 84-98, 110-124, 130-144, 131-145, 132-146 and 133-147.
13 - 14 . (canceled)
15 . A pharmaceutical composition comprising a plurality of peptides according to claim 11 , each peptide comprising a T cell epitope for the disease.
16 . A method for treating and/or preventing a disease in a subject in need of same which comprises the step of administering a peptide according to claim 11 to the subject.
17 . A method according to claim 16 , which comprises the following steps:
(i) identifying an antigen for the disease (ii) identifying an apitope for the antigen; and (iii) administering the apitope to the subject.
18 . A method according to claim 16 wherein the peptide or apitope is administered in multiple doses.
19 . A method according to claim 16 , wherein the peptide or apitope is administered intranasally.Join the waitlist — get patent alerts
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