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The New England journal of medicine · 2024

Aggressive Lymphoma after CD19 CAR T-Cell Therapy.

СтатьяКлинический случайНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Kobbe Guido, Brüggemann Monika, Baermann Ben-Niklas, Wiegand Laura, Trautmann Heiko, Yousefian Schayan, Libertini Silvana, Menssen Hans D, Maier Harald J, Ulrich Peter, Gao Jingbo, Bruch Peter-Martin, Liebers Nora, Radujkovic Aleksandar, Seifert Marc, Schniederjohann Christina, Paramasivam Nagarajan, Fitzgerald Donnacha, Seidel Maximilian, Esposito Irene, Germing Ulrich, Cadeddu Ron-Patrick, Nachtkamp Kathrin, Jäger Paul, Ulrych Thomas, Fischer Johannes C, Rox Jutta M, Giesel Frederik, Koch Raphael, Antoch Gerald, Distler Jörg H W, Meuth Sven G, Jacobsen Malte, Hübschmann Daniel, Lu Junyan, Iaccarino Ingram, Haas Simon, Damm Frederik, Dietrich Sascha

Аннотация

The development of a fatal, clonal, autonomously proliferating CD4-CD8- chimeric antigen receptor (CAR)+ peripheral T-cell lymphoma (PTCL) occurred 1 month after a patient received treatment with tisagenlecleucel for relapsed primary central nervous system lymphoma. The PTCL had a clonal T-cell receptor rearrangement, which was already detectable in the apheresis product for CAR T-cell manufacturing and 7 months earlier for autologous transplantation. Somatic DNMT3A and TET2 mutations in CD34+ stem cells and their progeny were detected in the PTCL, in the apheresis specimen that was obtained for CAR T-cell production, and in the autotransplant. The PTCL harbored an additional somatic TET2 mutation, which was already detectable in the CAR T-cell apheresis product and the final CAR T-cell product at very low frequencies, providing evidence that clonal hematopoiesis had contributed to lymphomagenesis.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты