US2004146505A1PendingUtilityA1
Substances
Priority: Jan 26, 2001Filed: Jan 28, 2002Published: Jul 29, 2004
Est. expiryJan 26, 2021(expired)· nominal 20-yr term from priority
A61P 35/00A61K 2039/53A61P 37/04C07K 16/00C07K 16/4266C07K 2317/52A61K 2039/505Y10S530/806C07K 2317/74A61K 39/00A61K 39/395
36
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Claims
Abstract
The invention relates to the use of a polypeptide which comprises i) a first portion comprising the part of human Fc which binds to CD64, and ii) a second portion comprising one or more heterologous T cell epitopes for stimulating a cytotoxic T cell response. The polypeptide may be an antibody which may be used to stimulate an cytotoxic T cell response against pathogens and tumour cells in patients in need of such treatment.
Claims
exact text as granted — not AI-modified1 . The use of a polypeptide which comprises (i) a first portion comprising the part of human Fc which binds to CD64, and (ii) a second portion comprising one or more heterologous T cell epitopes in the manufacture of a medicament for stimulating a cytotoxic T cell response.
2 . The use as claimed in claim 1 , wherein the first portion comprises the Fc segment of human IgG.
3 . The use as claimed in claim 2 , wherein the IgG is human IgG1.
4 . The use as claimed in claim 3 , wherein the first portion comprises human FcγI.
5 . The use as claimed in any one of claims 1 to 4 , wherein the second portion is a Fab fragment.
6 . The use as claimed in claim 5 , wherein the Fab fragment is non-human, preferably from mouse.
7 . The use as claimed claim 5 , wherein the Fab fragment is from human.
8 . The use as claimed in any preceding claim wherein the heterologous T cell epitope is a pathogen epitope.
9 . The use as claimed in any of claims 1 to 7 , wherein the heterologous T cell epitope is a non-pathogen epitope.
10 . The use as claimed in claim 9 , wherein the non-pathogen epitope is a tumour epitope.
11 . The use as claimed in any preceding claim, wherein the polypeptide is a monoclonal antibody.
12 . The use as claimed in any one of claims 1 to 10 , wherein the polypeptide is a protein domain-Fc construct.
13 . The use as claimed in any preceding claim, wherein the medicament stimulates cytotoxic and helper T cell responses.
14 . The use as claimed in any preceding claim, wherein the medicament is for the treatment and/or prophylaxis of cancer.
15 . The use as claimed in any preceding claim, wherein the medicament is for intramuscular and/or intradermal administration.
16 . The use as claimed in any preceding claim further comprising the use of a nucleic acid which encodes a polypeptide which comprises (i) a first portion comprising the part of human Fc which binds to CD64, and (ii) a second portion comprising one or more heterologous T cell epitopes in the manufacture of a medicament for stimulating a cytotoxic T cell response.
17 . The use as claimed in any preceding claim, wherein the medicament further comprises an adjuvant
18 . A method for stimulating a cytotoxic T cell response in a patient such as a mammal, including human, comprising administering to the patient a therapeutically effective amount of a polypeptide which comprises (i) a first portion comprising the part of human Fc which binds to CD64, and (ii) a second portion comprising one or more heterologous T cell epitopes.
19 . A method as claimed in claim 18 modified by the features of any one of claims 1 to 17 .
20 . The constant region of a human antibody capable of binding CD64 fused to a polypeptide comprising one or more T cell.
21 . The constant region of a human antibody as claimed in claim 20 , modified by the features of any one of claims 2 - 10 .
22 . A nucleic acid encoding the constant region of a human antibody as claimed in claim 20 or claim 21.Cited by (0)
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