Müllerian inhibiting substance type 2 receptor (MISIIR)-specific CAR T cells for the treatment of ovarian cancer and other gynecologic malignancies

US12559563B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12559563-B2
Application numberUS-202017603539-A
CountryUS
Kind codeB2
Filing dateApr 14, 2020
Priority dateApr 15, 2019
Publication dateFeb 24, 2026
Grant dateFeb 24, 2026

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

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The present disclosure provides modified immune cells or precursors thereof (e.g., modified T cells) comprising a chimeric antigen receptor (CAR) having affinity for Müllerian inhibiting substance type 2 receptor (MISIIR). Compositions and methods of treatment of diseases and disorders, such as ovarian and other gynecologic cancers, are also provided. Additionally provided herein are modified immune cells or precursor cells thereof comprising a nucleic acid encoding a CAR having affinity for Müllerian inhibiting substance type 2 receptor (MISIIR).

First claim

Opening claim text (preview).

What is claimed: 1 . A modified immune cell or precursor cell thereof, comprising: a chimeric antigen receptor (CAR), wherein the CAR comprises an antigen binding domain having affinity for Müllerian inhibiting substance type 2 receptor (MISIIR), a transmembrane domain, and an intracellular domain, wherein the CAR comprises the amino acid sequence set forth in SEQ ID NO: 2, and/or is encoded by the nucleotide sequence set forth in SEQ ID NO: 1. 2 . The modified immune cell or precursor cell of claim 1 , wherein: (a) the cell is an autologous cell; and/or (b) the cell is isolated from a human subject; and/or (c) the cell is a modified T cell. 3 . A method of treating cancer in a subject in need thereof, the method comprising administering to the subject the modified immune or precursor cell of claim 1 . 4 . A method of treating a cancer in a subject in need thereof, comprising administering to the subject a modified T cell comprising: a chimeric antigen receptor (CAR), wherein the CAR comprises an antigen binding domain having affinity for Mullerian inhibiting substance type 2 receptor (MISIIR), a transmembrane domain, and an intracellular domain, wherein the CAR comprises the amino acid sequence set forth in SEQ ID NO: 2, and/or is encoded by the nucleotide sequence set forth in SEQ ID NO: 1. 5 . The method of claim 4 , wherein, (a) the cancer is selected from the group consisting of ovarian cancer, endometrial cancer, uterine sarcoma, cervical carcinoma, breast cancer, lung cancer, prostate cancer, ocular melanoma, a MISIIR-expressing tumor, and ovarian cancer; and/or (b) the modified T cell is human; and/or (c) the modified T cell is autologous; and/or (d) the subject is human.

Assignees

Inventors

Classifications

  • CD19 or B4 · CPC title

  • Receptors, cell surface antigens or cell surface determinants · CPC title

  • Chimeric antigen receptors [CAR] · CPC title

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

  • Reproductive system, e.g. uterus, ovaries, cervix or testes · CPC title

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What does patent US12559563B2 cover?
The present disclosure provides modified immune cells or precursors thereof (e.g., modified T cells) comprising a chimeric antigen receptor (CAR) having affinity for Müllerian inhibiting substance type 2 receptor (MISIIR). Compositions and methods of treatment of diseases and disorders, such as ovarian and other gynecologic cancers, are also provided. Additionally provided herein are modified i…
Who is the assignee on this patent?
Univ Pennsylvania
What technology area does this patent fall under?
Primary CPC classification C07K14/7051. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 24 2026 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).