Case Report: Fatal cytomegalovirus pneumonia after CAR-T cell therapy in the long-term follow-up

Front Immunol. 2023 Oct 2:14:1226148. doi: 10.3389/fimmu.2023.1226148. eCollection 2023.

Abstract

Introduction: The rapidly developed CAR-T cell therapy has a unique profile of side effects, which perhaps has not been totally realized and understood, especially the late-phase toxicity. CMV is prevalent world-wide and establishes a life-long latency infection. It can lead to life-threatening complications in immunocompromised host, and little is known about CMV disease in patients after CAR-T cell therapy. Here, we report a patient who developed possible CMV-pneumonia three months after anti-CD19 and anti-CD22 CAR-T cell therapy for relapsed B-ALL, contributing to the understanding of severe side-effects mediated by virus infection or reactivation in patients receiving CAR-T cell infusion.

Case presentation: A 21-year old male patient with relapsed B-ALL received anti-CD19/22 CAR-T cell therapy, and achieved complete remission 2 weeks after the infusion. However, three months later, the patient was hospitalized again with a 10-day history of fever and cough and a 3-day history of palpitations and chest tightness. He was diagnosed with possible CMV pneumonia. Under treatment with antiviral medicine (ganciclovir/penciclovir), intravenous gamma globulin and methylprednisolone and the use of BiPAP ventilator, his symptoms improved, but after removing penciclovir his symptoms went out of control, and the patient died of respiratory failure 22 days after admission.

Conclusion: CMV infection/reactivation can occur in patients long after receiving anti-CD19/22 CAR-T cell therapy, and induce fatal pneumonia, which reminds us of the late side effects associated with immunosuppression after CAR-T cell infusion.

Keywords: B-ALL; CAR-T cell therapy; CMV disease; CMV pneumonia; case report.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell- and Tissue-Based Therapy
  • Cytomegalovirus
  • Cytomegalovirus Infections* / etiology
  • Cytomegalovirus Infections* / therapy
  • Follow-Up Studies
  • Humans
  • Male
  • Pneumonia* / etiology
  • Receptors, Chimeric Antigen*
  • Young Adult

Substances

  • Receptors, Chimeric Antigen

Grants and funding

This work was supported by the Key Program of the National Natural Science Foundation of China (81830008 and 81630006), the National Natural Science Foundation of China (81600120 and 81670152) and the Key program of Technological Innovation fund of Hubei Province (2018ACA140).