US2006073126A1PendingUtilityA1
Cytotoxic T lymphocyte
Est. expiryOct 1, 2024(expired)· nominal 20-yr term from priority
A61P 31/00A61P 35/00A61P 37/04A61K 48/00A61K 2039/5158A61K 40/46A61K 40/45A61K 40/428A61K 40/24A61K 40/42A61K 40/11A61K 2039/5156A61K 2039/5154C12N 5/0636A61K 39/0011A61K 39/00
50
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Claims
Abstract
The present invention relates to a T lymphocyte having an activity to induce a T lymphocyte recognizing an antigen and a technique to use the T lymphocyte.
Claims
exact text as granted — not AI-modified1 . An RNA-introduced T lymphocyte into which an RNA encoding an antigen of interest is introduced, which has an activity to induce a T lymphocyte which recognizes the antigen.
2 . The RNA-introduced T lymphocyte according to claim 1 , which is a CD4-positive cell activated with phytohemagglutinin.
3 . A method for inducing a T lymphocyte, comprising using, as an antigen-presenting cell, an RNA-introduced T lymphocyte into which an RNA encoding an antigen of interest is introduced, to induce a T lymphocyte which recognizes the antigen.
4 . The method according to claim 3 , wherein the RNA-introduced T lymphocyte is a CD4-positive cell activated with phytohemagglutinin.
5 . The method according to claim 3 , wherein the T lymphocyte which recognizes the antigen is a cytotoxic T lymphocyte positive to CD8.
6 . The method according to any one of claims 3 to 5 , wherein the antigen is a tumor-associated antigen or an antigen of an infectious microorganism.
7 . The method according to claim 6 , wherein the RNA is an RNA prepared from a cancer tissue.
8 . The method according to claim 6 , wherein the antigen is EBNA3A and/or CMVpp65.
9 . An immune inducer containing the RNA-introduced T lymphocyte as defined in claim 1 or 2 .
10 . A therapeutic agent for cancer or infectious disease, containing the T lymphocyte obtained by the method of any one of claims 3 to 8 as an active ingredient.
11 . A cytotoxic T lymphocyte which recognizes a cell presenting on the surface thereof a complex of a human major histo-compatibility antigen (HLA)-A24-restricted antigen peptide represented by SEQ ID NO: 1 or 2 and an HLA-A24 molecule or a complex of a functional derivative of the HLA-A24-restricted antigen peptide and an HLA-A24 molecule, and which is CD8-positive.
12 . A therapeutic agent for cancer, containing the cytotoxic T lymphocyte of claim 11 .
13 . An inducer of the cytotoxic T lymphocyte of claim 11 , containing at least one peptide selected from the group consisting of a human major histo-compatibility antigen (HLA)-A24-restricted antigen peptide represented by SEQ ID NO: 1 or 2 and a functional derivative thereof as an active ingredient.
14 . A therapeutic agent for cancer, containing a human major histo-compatibility antigen (HLA)-A24-restricted antigen peptide represented by SEQ ID NO: 1 or 2 and a functional derivative thereof as an active ingredient.
15 . A tetramer for detecting a T cell receptor possessed by the cytotoxic T lymphocyte of claim 11 , comprising a human major histo-compatibility antigen (HLA)-A24-restricted antigen peptide represented by SEQ ID NO: 1 or 2 or a functional derivative thereof.Join the waitlist — get patent alerts
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