不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A case report of prolonged viral shedding of SARS-CoV-2 in a patient who receive ibrutinib for CLL therapy.
A case report of prolonged viral shedding of SARS-CoV-2 in a patient who receive ibrutinib for CLL therapy.
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接受B细胞免疫抑制治疗的患者已被证明存在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的持续感染。在本报告中,一名因慢性淋巴细胞白血病接受ibrutinib治疗的女性经历了超过40天的2019冠状病毒病(COVID-19)感染。出乎意料的是,她的外周血实验显示SARS-CoV-2特异性抗体水平正常,CD19+ B细胞百分比相对升高,而NK细胞、CD4+ T细胞和CD8+ T细胞百分比明显下降。对该患者进一步的SARS-CoV-2特异性T细胞分析表明,产生SARS-CoV-2特异性IFN-γ、TNF-α或IL-2的CD4+ T细胞或CD8+ T细胞百分比显著下降。最值得注意的是,停用ibrutinib十天后,SARS-CoV-2 PCR转为阴性,外周血CD4+ T细胞和CD8+ T细胞比例降低也得到恢复。
我们的研究预测,耗竭B细胞功能的治疗可能在长COVID-19的发生中发挥相当重要的作用,而T细胞亚群分布异常可能是其潜在机制。
Patients on B cell immunosuppressive treatments have been shown to have persistent infection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In this report, a woman treated with ibrutinib for chronic lymphocytic leukemia experienced more than 40 days of coronavirus disease 2019 (COVID-19) infection.
Unexpectedly, her peripheral blood experiments showed a normal SARS-CoV-2-specific antibody level and a relatively elevated percentage of CD19 + B cells, while an obvious decrease in the percentages of NK cells, CD4 + T cells and CD8 + T cells.
Further SARS-CoV-2-specific T cell analysis in this patient indicated a significant decrease in the percentage of SARS-CoV-2-specific IFN-γ, TNF-α or IL-2 producing CD4 + T or CD8 + T cells. Most notably, ten days after the cease of ibrutinib, the PCR for SARS-CoV-2 turned negative and the reduced proportions of peripheral CD4 + T cells and CD8 + T cells recovered.
Our research predicted that the depleted B-cell function therapies may play considerable role in the development of long COVID-19 and the abnormal T-cell subset distribution might be the underlying mechanism.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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