Combined chimeric antigen receptor targeting CD19 and CD20 and application thereof
US-2024139243-A1 · May 2, 2024 · US
US10196432B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10196432-B2 |
| Application number | US-91267006-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 5, 2006 |
| Priority date | Sep 5, 2005 |
| Publication date | Feb 5, 2019 |
| Grant date | Feb 5, 2019 |
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The present invention relates to immunotherapeutic methods, and molecules and cells for use in immunotherapeutic methods. In particular, the present invention relates to the immunotherapy of cancer. The present invention furthermore relates to tumour-associated T-helper cell peptide epitopes, alone or in combination with other tumour-associated peptides, that serve as active pharmaceutical ingredients of vaccine compositions which stimulate anti-tumour immune responses. In particular, the present invention relates to 49 novel peptide sequences derived from HLA class II molecules of human tumour cell lines which can be used in vaccine compositions for eliciting anti-tumour immune responses.
Opening claim text (preview).
The invention claimed is: 1. A composition comprising an isolated tumor associated peptide consisting of the amino acid sequence selected from the group consisting of SEQ ID NO: 2 to SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 32, and SEQ ID NO: 34 to SEQ ID NO: 48, a pharmaceutically acceptable carrier, and at least one immune-stimulating adjuvant, wherein the immune-stimulating adjuvant is selected from the group consisting of incomplete Freund's adjuvant, complete Freund's adjuvant, liposomal formulations, Bacillus Calmette-Gudrin (BCG), alum, Detox, CpG oligonucleotides, Interleukin-12 (IL-12), Interleukin-2 (IL-2) and stabilized RNA and wherein the peptide is produced by solid phase peptide synthesis and cleaved from a resin support by treatment with trifluoroacetic acid. 2. The composition according to claim 1 , wherein the peptide has the ability to bind human major histocompatibility complex (MHC) class-II molecule HLA-DRB*0101 and has the ability to bind to at least one additional molecule of the human major histocompatibility complex (MHC) class-II. 3. The composition of claim 1 , wherein the composition further comprises at least one excipient selected from a buffer, a binding agent, a blasting agent, a diluent, a flavour and a lubricant. 4. A fusion protein consisting of a tumour associated peptide consisting of the amino acid sequence selected from the group consisting of SEQ ID NO: 2 to SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 32, and SEQ ID NO: 34 to SEQ ID NO: 48 and the 80 N-terminal amino acids of the HLA-DR antigen-associated invariant chain (Ii).
Immunostimulants · CPC title
Immunomodulators · CPC title
Antineoplastic agents · CPC title
from animals; from humans {(enzyme inhibitors A61K38/005)} · CPC title
Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title
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