CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:SARS-CoV-2 vaccine response in CAR T-cell therapy recipients: A systematic review and preliminary observations.
SARS-CoV-2 vaccine response in CAR T-cell therapy recipients: A systematic review and preliminary observations.
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不断演变的数据表明,SARS-CoV-2 疫苗应答在异基因造血细胞移植(HCT)受者中减弱。CAR-T 细胞治疗中的疫苗应答尚不清楚,且可能更为减弱。
我们手动检索了重要数据库,并确定了 5 项研究,这些研究迄今共报告了 70 例 CAR-T 受者的 COVID-19 疫苗应答。所有 5 项研究的累计体液缓解率为 31%。
然而,由于体液应答测量单位不统一且缺乏外部验证,结果无法推广。各研究在 CAR-T 后接种疫苗的时间、疫苗剂量之间的间隔、应答评估平台、疫苗平台以及接种前免疫状态方面存在异质性。本文进一步综述了独立影响预防 COVID-19 疫苗应答的 CAR-T 相关因素。
我们得出结论,鉴于样本量小、免疫测定方法不同、缺乏标准定义和 SARS-CoV-2 免疫应答的临床相关性以及缺乏细胞应答等局限性,必须谨慎解读这些结果。在大规模、同质性前瞻性数据可用之前,这些初步观察结果将有助于移植和感染性疾病临床医生在为这一深度免疫抑制患者群体提供诊疗时进行决策。
Evolving data suggest that SARS-CoV-2 vaccine responses are blunted in allogeneic hematopoeitic cell transplant (HCT) recipients. Responses to the vaccine in chimeric antigen receptor T-cell (CAR-T) therapy are unknown and are likely to be even more diminished.
We manually searched vital databases and identified 5 studies that have so far reported COVID-19 vaccine response in a total of 70 CAR-T recipients. The cumulative humoral response rate across all 5 studies was 31%.
However, the results are not generalizable due to non-standardized units of humoral response measurement and a lack of external validation. Heterogeneity existed in studies regarding the timing of vaccination post-CAR-T, intervals between the vaccine doses, platforms of response assessment, vaccine platforms, and pre-vaccine immune status. CAR-T-related factors that independently impact vaccine response to prevent COVID-19 have further been reviewed.
We conclude that the results must be interpreted with caution given the limitations of small sample sizes, differences in immunoassays, lack of standard definitions and clinical correlates of SARS-CoV-2 immune response, and lack of cellular responses. Until large-scale, homogenous prospective data become available, these preliminary observations will help transplant and infectious disease clinicians with their decision-making while providing care to this profoundly immunosuppressed cohort of patients.
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