Chimeric Antigen Receptor and Car-T Cells That Bind Cxcr5

Publication: WO2019038368A1
Published: 2019-02-28
Family Size: 13
Granted: Yes (4/13)

Simple SummaryContent extracted from patent full text and abstract with AI.

This invention relates to a novel chimeric antigen receptor (CAR) that specifically binds the human CXC chemokine receptor type 5 (CXCR5). The invention includes the design of an antibody-based CAR (including nucleic acid constructs) and the generation of genetically modified immune cells, preferably CAR-T cells, that can recognize and destroy cells expressing CXCR5. These CAR-T cells are intended for the treatment of diseases involving CXCR5-positive pathogenic cells, such as certain types of lymphomas (especially mature B cell non-Hodgkin's lymphoma), some autoimmune diseases, and possibly HIV reservoirs.

Use CasesContent extracted from patent full text and abstract with AI.

  • Targeted immunotherapy for mature B cell non-Hodgkin’s lymphoma (B-NHL), including difficult-to-treat or relapsed cases.
  • Treatment of other B cell lymphoproliferative disorders such as acute lymphoblastic leukemia (B-ALL), chronic lymphocytic leukemia (CLL), follicular lymphoma, mantle cell lymphoma, and diffuse large B cell lymphoma.
  • Targeted therapy for T cell non-Hodgkin's lymphoma and other T cell lymphoproliferative disorders expressing CXCR5.
  • Adoptive cell therapy for autoantibody-dependent autoimmune diseases, including systemic lupus erythematosus (SLE) and rheumatoid arthritis.
  • Potential treatment of HIV infection by targeting CXCR5-positive T follicular helper cell reservoirs of the virus.

BenefitsContent extracted from patent full text and abstract with AI.

  • Provides a new therapeutic option for cancers and autoimmune diseases that express CXCR5, especially where current treatments fail or cause significant side effects.
  • Effective against tumors or pathogenic cells even when traditional targets like CD19 are lost due to resistance or mutation.
  • Spares normal hematopoietic cells, reducing off-target toxicity compared to existing CAR-T therapies.
  • Applicable to patients who cannot tolerate chemotherapy or stem cell transplantation, such as elderly or fragile individuals.
  • Can be used as a salvage therapy or as a bridging treatment before other interventions.
  • High specificity and avidity for CXCR5 minimizes risk of harming healthy (CXCR5-negative) tissues.
  • Flexible CAR design allows adaptation to different patient needs or disease circumstances.

Technical Classifications (CPCs)

Main Classifications

Chemistry & Materials Science

Health, Food & Consumer Tech

Sub Classifications

Biochemistry, Beer & Spirits

Medical & Vet Science

Organic Chemistry

CPC Codes

A61K40/11A61K40/31A61K40/4211A61K40/4219A61P35/00C07K14/7051C07K14/70517C07K14/70521C07K14/70578C07K16/2866C12N5/0636C12N5/0646

Inventors & Applicants

Applicants

Max Delbrueck Centrum Fuer Molekulare Medizin Helmholtz Gemeinschaft

Humboldt Univ zu Berlin

Patent Abstract

The invention relates to an isolated chimeric antigen receptor polypeptide (CAR), wherein the CAR comprises an extracellular antigen-binding domain, comprising an antibody or antibody fragment that binds a human CXC chemokine receptor type 5 (CXCR5) protein. The invention further relates to a nucleic acid molecule encoding the CAR of the invention, a genetically modified immune cell, preferably a T cell, expressing the CAR of the invention and the use of said cell in the treatment of a medical disorder associated with the presence of pathogenic cells expressing CXCR5, preferably pathogenic mature B cells and/or memory B cells, and/or pathogenic T cells and/or T follicular helper cells, in particular mature B cell non-Hodgkin's lymphoma (B-NHL), T cell non-Hodgkin's lymphoma, or autoantibody-dependent autoimmune disease, preferably selected from systemic lupus erythematosus (SLE) or rheumatoid arthritis.

Key Information

Publication No.

WO2019038368A1

Family ID

59713849

Publication Date

2019-02-28

Application No.

EP2018072750W

Application Date

2018-08-23

Priority Date

2017-08-23

Granted

Yes (4/13)

Possible Cooperation

For further information please contact the transfer office.