Case report: A novel third-generation anti-CD19/CD22 CAR T-cells combined with auto-HSCT for relapsed Burkitt lymphoma

Front Immunol. 2024 Dec 9:15:1497736. doi: 10.3389/fimmu.2024.1497736. eCollection 2024.

Abstract

This study explores a novel therapeutic strategy for relapsed/refractory (R/R) Burkitt lymphoma (BL) by integrating autologous hematopoietic stem cell transplantation (ASCT) with tandem anti-CD19/CD22 chimeric antigen receptor (CAR) T cell therapy. A 20-year-old Asian male with refractory BL, whose lymphoma had not responded to multiple chemoimmunotherapy regimens, received myeloablative ASCT followed three days later by infusion of a novel third-generation CAR T cells engineered with CD28 and CD3ζ signaling domains, along with a TLR2 costimulatory domain. This resulted in sustained complete remission at the 306-day follow-up, without experiencing any severe complications. This case suggests that combining myeloablative ASCT with tandem anti-CD19/CD22 CAR T cell therapy could be an effective approach for R/R BL, warranting further clinical validation.

Keywords: CAR T-cell therapy; CD19/CD22 dual target; autologous hematopoietic stem cell transplantation; immunotherapy; relapsed/refractory Burkitt lymphoma.

Publication types

  • Case Reports

MeSH terms

  • Antigens, CD19* / immunology
  • Burkitt Lymphoma* / immunology
  • Burkitt Lymphoma* / therapy
  • Combined Modality Therapy
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Immunotherapy, Adoptive* / methods
  • Male
  • Neoplasm Recurrence, Local / immunology
  • Neoplasm Recurrence, Local / therapy
  • Receptors, Chimeric Antigen* / genetics
  • Receptors, Chimeric Antigen* / immunology
  • Sialic Acid Binding Ig-like Lectin 2* / immunology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / transplantation
  • Transplantation, Autologous
  • Treatment Outcome
  • Young Adult

Substances

  • Antigens, CD19
  • Receptors, Chimeric Antigen
  • Sialic Acid Binding Ig-like Lectin 2
  • CD22 protein, human
  • CD19 molecule, human

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.