H3.3 ctl peptides and uses thereof

US2025090636A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2025090636-A1
Application numberUS-202418667792-A
CountryUS
Kind codeA1
Filing dateMay 17, 2024
Priority dateMay 5, 2015
Publication dateMar 20, 2025
Grant date

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Abstract

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Peptides that generate an immune response to glioma-related H3.3 proteins and methods of their use are provided.

First claim

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1 - 57 . (canceled) 58 . A polynucleotide sequence encoding TCR or a fragment thereof, which binds to a peptide/major histocompatibility complex (MHC) complex, wherein the TCR or the fragment thereof binds to a histone H3 variant H3.3 peptide, and wherein the TCR or fragment thereof comprises: (a) a TCR alpha chain or fragment thereof comprising complementarity determining regions (CDRs) 1, 2, and 3 comprising SEQ ID NOs: 12, 13, and 14, respectively; and (b) a TCR beta chain or fragment thereof comprising CDRs 1, 2, and 3 comprising SEQ ID NOs: 15, 16, and 17, respectively. 59 . The polynucleotide sequence according to claim 58 , wherein the TCR alpha chain comprises the amino acid sequence set forth in SEQ ID NO: 8, and the TCR beta chain comprises the amino acid sequence set forth in SEQ ID NO: 10. 60 . The polynucleotide sequence according to claim 58 , wherein the polynucleotide sequence comprises one or more heterologous sequences. 61 . The polynucleotide sequence according to claim 60 , wherein the one or more heterologous sequences is a promoter. 62 . The polynucleotide sequence according to claim 60 , wherein the one or more heterologous sequences encodes a self-cleaving peptide. 63 . The polynucleotide sequence according to claim 62 , wherein the self-cleaving peptide is a porcine teschovirus-1 2A (P2A) peptide. 64 . A vector comprising the polynucleotide sequence according to claim 58 . 65 . The vector according to claim 64 , wherein the vector is a viral vector. 66 . The vector according to claim 65 , wherein the viral vector is a lentiviral vector. 68 . A composition comprising the vector according to claim 64 . 69 . The polynucleotide sequence according to claim 58 , wherein the peptide in the peptide/MHC complex comprises the amino acid sequence (R/A) MSAP (S/A) TGGV (SEQ ID NO: 1). 70 . The polynucleotide sequence according to claim 69 , wherein the peptide in the peptide/MHC complex consists of 10-12 amino acids. 71 . The polynucleotide sequence according to claim 70 , wherein the amino acid sequence is RMSAPSTGGV (SEQ ID NO: 2).

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Inventors

Classifications

  • Nervous system antigens · CPC title

  • T-cell receptors [TCR] · CPC title

  • T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells · CPC title

  • Brain; Nervous system · CPC title

  • characterized by the route of administration · CPC title

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What does patent US2025090636A1 cover?
Peptides that generate an immune response to glioma-related H3.3 proteins and methods of their use are provided.
Who is the assignee on this patent?
Univ California
What technology area does this patent fall under?
Primary CPC classification C12N5/0638. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Mar 20 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).