Kyverna is on the forefront of developing advanced cellular therapies designed to be selective, potent, and durable with sustained therapeutic effect. Our therapeutic platform leverages T cell engineering to target the underpinnings of autoimmunity, including chimeric antigen receptor T (CAR T) cells.
Creating “smarter” CAR T cells
Leveraging advances in CAR T engineering and insights from the use of conventional CAR T cell therapies for cancer, Kyverna is building a robust collection of cell therapy assets and tools to address multiple targets implicated in the pathogenesis of autoimmune diseases.
Targeted cellular therapies that address the complexities of the immune system and its various disease mechanisms
Using our T cell engineering platform, we are programming immune cells with instructions to eliminate pathogenic cells in the diseased tissues in which they are exerting their deleterious effects. Our product candidates leverage our deep understanding of the pathogenesis of autoimmune diseases to select the appropriate technology for each disease.
CAR T cells with the potential for therapeutic breakthrough in B-cell driven autoimmune diseases.
Kyverna is the exclusive world-wide licensee of a next-generation CAR T construct targeting CD19 for use in autologous (KYV-101) and allogeneic (KYV-201) cell therapies for B-cell driven autoimmune diseases. Designed with favorable characteristics for use in autoimmunity, KYV-101 and KYV-201 combine a fully human anti-CD19 CAR with costimulatory domains designed to minimize cytokine release, maximize B-cell depletion, and improve clinical tolerability.
In a 20-patient Phase 1/2 study in oncology, expected anti-lymphoma activity was associated with a significant reduction of cytokines released. Of note, in patients who received the new construct, a ten-fold reduction in the rate of severe neurological toxicity was observed compared to patients who received T cells transduced with an earlier generation, murine-based construct. The fully human anti-CD19 CAR also translated into reduced immunogenicity that favorably impacted cell persistence at one month.1
Preclinically, CD19-targeted CAR T-cell therapies have been shown to induce deep and complete B cell depletion in both the circulation and tissues resulting in striking efficacy in disease models supporting the promise of a transformative impact for the approach in patients with B-cell driven autoimmune diseases.2 B cells are important for disease pathogenesis, and tissue-based B cells are resistant to depletion by existing agents. Overall, existing approaches to address B-cell driven autoimmune diseases are often limited by either modest effects, leading to resistant and uncontrolled disease, or significant treatment-related morbidity and mortality.
Prior generations of anti-CD19 CAR T cells rely on mouse-derived CD19 binding domains and are associated with high levels of cytokine production. Importantly, high cytokine production has been shown to translate to cytokine release syndrome.3 In contrast, KYV-101 and KYV-201 use a fully human anti-CD19 CAR and costimulatory domains designed to minimize cytokine production. These two combined attributes are of particular importance for use in autoimmune disease patients because (i) autoimmune disease patients are known to mount immune reactions against foreign mouse proteins and (ii) the cytokines released in high amounts by traditional CAR T cells are the same cytokines that can drive autoimmune diseases. The impact our anti-CD19 CAR has had on reducing clinically relevant immunogenicity and on minimizing the production of disease-driving cytokines has been extensively characterized.1
- Brudno J et al. Safety and feasibility of anti-CD19 CAR T cells with fully human binding domains in patients with B-cell lymphoma. Nature Medicine 2020;26:270-280.
- Kansal R et al. Sustained B cell depletion by CD19-targeted CAR T cells is a highly effective treatment for murine lupus. Science Translational Medicine 2019; 11(482):eaav1648.
- Frigault et. al. State of the art in CAR T cell therapy for CD19+ B cell malignancies. JCI 2020; 130(4):1586-1594.