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:Treatment of chronic COVID-19 with convalescent/postvaccination plasma in patients with hematologic malignancies.
Treatment of chronic COVID-19 with convalescent/postvaccination plasma in patients with hematologic malignancies.
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免疫功能低下患者清除SARS-CoV-2失败的风险很高。迁延性COVID-19构成健康风险和管理难题,因为癌症治疗往往不得不中断。随着SARS-CoV-2的演变,出现了新的关注变异株,能够逃逸现有的单克隆抗体。
此外,抗病毒治疗会促进SARS-CoV-2逃逸突变,尤其是在免疫功能低下患者中。这些患者经常遭受迁延性感染。对于持续性COVID-19感染,尚未建立成功的治疗方案。
在此,我们报告了21例免疫功能低下COVID-19患者系列——其中大多数为血液系统恶性肿瘤——接受近期康复者或疫苗接种者血浆或两者联合治疗的情况。重复给予含SARS-CoV-2抗体的血浆可使21例免疫功能低下患者中的16例清除SARS-CoV-2感染,即使COVID-19特异性治疗未能诱导持续病毒清除或改善SARS-CoV-2感染的临床病程。10例患者为主要应答者,定义为首次给予康复者和/或疫苗接种者血浆(C/VP)后delta(d)Ct增加>=5。在主要应答亚组中,SARS-CoV-2 PCR Ct值平均从中位数22.55(IQR=19.10-24.25)升高至中位数29.57(IQR=27.55-34.63;p=<.0001)。
此外,当第二次接受C/VP治疗时,即使初始无应答者中也有5例中的4例显示Ct值从中位数23.13(IQR=17.75-28.05)升高至中位数32.79(IQR=31.75-33.75;p=.013)。
我们的结果表明,C/VP可能是对血液系统恶性肿瘤且对抗病毒治疗无应答患者COVID-19感染的一种可行治疗方法。
Immunocompromised patients are at high risk to fail clearance of SARS-CoV-2. Prolonged COVID-19 constitutes a health risk and a management problem as cancer treatments often have to be disrupted. As SARS-CoV-2 evolves, new variants of concern have emerged that evade available monoclonal antibodies.
Moreover, antiviral therapy promotes SARS-CoV-2 escape mutations, particularly in immunocompromised patients. These patients frequently suffer from prolonged infection. No successful treatment has been established for persistent COVID-19 infection.
Here, we report on a series of 21 immunocompromised patients with COVID-19-most of them hematologic malignancies-treated with plasma obtained from recently convalescent or vaccinated donors or a combination thereof. Repeated dosing of SARS-CoV-2-antibody-containing plasma could clear SARS-CoV-2 infection in 16 out of 21 immunocompromised patients even if COVID-19-specific treatments failed to induce sustained viral clearance or to improve clinical course of SARS-CoV-2 infection.
Ten patients were major responders defined as an increase delta(d)Ct of > = 5 after the first administration of convalescent and/or vaccinated plasma (C/VP). On average, SARS-CoV-2 PCR Ct values increased from a median value of 22. 55 (IQR = 19. 10-24. 25) to a median value of 29. 57 (IQR = 27. 55-34. 63; p = <. 0001) in the major response subgroup.
Furthermore, when treated a second time with C/VP, even 4 out of 5 of the initial nonresponders showed an increase in Ct-values from a median value of 23. 13 (IQR = 17. 75-28. 05) to a median value of 32. 79 (IQR = 31. 75-33. 75; p = . 013).
Our results suggest that C/VP could be a feasible treatment of COVID-19 infection in patients with hematologic malignancies who did not respond to antiviral treatment.
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