Soukaina Sabir, Odelaisy León-Triana, Sergio Serrano, Roberto Barrio, Victor M. Pérez-García
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引用次数: 0
Abstract
CAR-T cell therapies have demonstrated significant success in treating B-cell
leukemia in children and young adults. However, their effectiveness in treating
B-cell lymphomas has been limited. Unlike leukemia, lymphoma often manifests as
solid masses of cancer cells in lymph nodes, glands, or organs, making these
tumors harder to access thus hindering treatment response. In this paper we
present a mathematical model that elucidates the dynamics of diffuse large
B-cell lymphoma and CAR-T cells in a lymph node. The mathematical model aids in
understanding the complex interplay between the cell populations involved and
proposes ways to identify potential underlying dynamical causes of treatment
failure. We also study the phenomenon of immunosuppression induced by tumor
cells and theoretically demonstrate its impact on cell dynamics. Through the
examination of various response scenarios, we underscore the significance of
product characteristics in treatment outcomes.
CAR-T 细胞疗法在治疗儿童和年轻人的 B 细胞白血病方面取得了巨大成功。然而,它们在治疗 B 细胞淋巴瘤方面的效果有限。与白血病不同,淋巴瘤通常表现为淋巴结、腺体或器官中的癌细胞团块,这使得肿瘤更难进入,从而阻碍了治疗反应。在本文中,我们提出了一个数学模型,该模型阐明了弥漫大B细胞淋巴瘤和CAR-T细胞在淋巴结中的动态变化。该数学模型有助于理解相关细胞群之间复杂的相互作用,并提出了识别治疗失败潜在潜在动态原因的方法。我们还研究了肿瘤细胞诱导的免疫抑制现象,并从理论上证明了它对细胞动力学的影响。通过对各种反应情况的研究,我们强调了产品特性在治疗结果中的重要性。