Humoral vaccine responses following Chimeric Antigen Receptor T-cell therapy for hematological malignancies - Summary - MDSpire

Humoral vaccine responses following Chimeric Antigen Receptor T-cell therapy for hematological malignancies

  • By

  • Sigrun Einarsdottir

  • Stephanie Lobaugh

  • Danny Luan

  • Marina Gomez-Llobell

  • Padmapriya Subramanian

  • Sean Devlin

  • David Chung

  • Parastoo B. Dahi

  • Lorenzo Falchi

  • Sergio Giralt

  • Heather Landau

  • Alexander M. Lesokhin

  • Richard Lin

  • Jennifer Lue

  • Sham Mailankody

  • M. Lia Palomba

  • Jae H. Park

  • Gilles Salles

  • Michael Scordo

  • Silvia Escribano-Serrat

  • Jaime Sanz

  • Kai Rejeski

  • Roni Shouval

  • Saad Usmani

  • Miguel-Angel Perales

  • Gunjan Shah

  • Zainab Shahid

  • July 2, 2025

  • 0 min

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Objective:

To investigate humoral immunity and vaccine responses to 12 vaccine-preventable infections in patients treated with CAR T-cell therapy, highlighting the significance of these responses in clinical outcomes.

Key Findings:
  • CD19 CAR T-cell therapy leads to nearly universal CD19 + B cell aplasia, while BCMA CAR T-cell therapy specifically depletes plasma cells.
  • Response rates to mRNA vaccines against COVID-19 were 27-34% for CD19 CAR recipients.
  • BCMA CAR T-cell recipients had lower seroprotection rates against vaccine-preventable infections compared to CD19 CAR T-cell recipients.
  • A significant percentage of infections post BCMA CAR T-cell therapy were vaccine preventable.
Interpretation:

The study highlights the distinct humoral deficiencies in patients receiving CD19 versus BCMA CAR T-cell therapies and underscores the need for tailored vaccination strategies.

Limitations:
  • Retrospective design may introduce bias.
  • Variability in clinical testing practices and timing of patient follow-up.
Conclusion:

Vaccination is crucial for infection prevention in CAR T-cell therapy recipients, and further studies are needed to optimize vaccination strategies post-treatment.

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