Melatonin as an immunomodulator in CD19-targeting CAR-T cell therapy: managing cytokine release syndrome

J Transl Med. 2024 Jan 14;22(1):58. doi: 10.1186/s12967-023-04779-z.

Abstract

Background: Chimeric antigen receptor CAR-T cell therapies have ushered in a new era of treatment for specific blood cancers, offering unparalleled efficacy in cases of treatment resistance or relapse. However, the emergence of cytokine release syndrome (CRS) as a side effect poses a challenge to the widespread application of CAR-T cell therapies. Melatonin, a natural hormone produced by the pineal gland known for its antioxidant and anti-inflammatory properties, has been explored for its potential immunomodulatory effects. Despite this, its specific role in mitigating CAR-T cell-induced CRS remains poorly understood.

Methods: In this study, our aim was to investigate the potential of melatonin as an immunomodulatory agent in the context of CD19-targeting CAR-T cell therapy and its impact on associated side effects. Using a mouse model, we evaluated the effects of melatonin on CAR-T cell-induced CRS and overall survival. Additionally, we assessed whether melatonin administration had any detrimental effects on the antitumor efficacy and persistence of CD19 CAR-T cells.

Results: Our findings demonstrate that melatonin effectively mitigated the severity of CAR-T cell-induced CRS in the mouse model, leading to improved overall survival outcomes. Remarkably, melatonin administration did not compromise the antitumor effectiveness or persistence of CD19 CAR-T cells, indicating its compatibility with therapeutic goals. These results suggest melatonin's potential as an immunomodulatory compound to alleviate CRS without compromising the therapeutic benefits of CAR-T cell therapy.

Conclusion: The study's outcomes shed light on melatonin's promise as a valuable addition to the existing treatment protocols for CAR-T cell therapies. By attenuating CAR-T cell-induced CRS while preserving the therapeutic impact of CAR-T cells, melatonin offers a potential strategy for optimizing and refining the safety and efficacy profile of CAR-T cell therapy. This research contributes to the evolving understanding of how to harness immunomodulatory agents to enhance the clinical application of innovative cancer treatments.

Keywords: Adoptive immunotherapy; CD19 antigen; Cell- and tissue-based therapy; Chimeric antigen receptors; Cytokine release syndrome; Melatonin; T lymphocytes.

MeSH terms

  • Animals
  • Antigens, CD19
  • Cell- and Tissue-Based Therapy
  • Cytokine Release Syndrome* / therapy
  • Immunologic Factors / pharmacology
  • Immunotherapy, Adoptive* / adverse effects
  • Melatonin* / pharmacology
  • Mice
  • Neoplasm Recurrence, Local
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen

Substances

  • Antigens, CD19
  • Immunologic Factors
  • Melatonin
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen