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通过PD-L1正电子发射断层扫描成像观察对COVID-19疫苗接种的反应。

Response to COVID-19 vaccination imaged by PD-L1 PET scanning.

作者信息

MacManus Michael P, Akhurst Tim, Lewin Sharon R, Hegi-Johnson Fiona

机构信息

Department of Radiation Oncology, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, Vic, 3000, Australia.

The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Australia.

出版信息

EJNMMI Rep. 2024 Jun 7;8(1):16. doi: 10.1186/s41824-024-00196-7.

Abstract

BACKGROUND

During a phase 0 clinical trial of an investigational programmed cell death ligand-1 (PD-L1) PET tracer in patients with non-small cell lung cancer (NSCLC), three patients received booster doses of COVID-19 vaccines before PD-L1 imaging.

METHODS

Five patients underwent whole-body PET/CT imaging with a novel PD-L1 tracer, constructed by attaching Zr to the anti PD-L1 antibody durvalumab. Intramuscular (deltoid) booster doses of mRNA BNT162b2 COVID-19 mRNA vaccine were coincidentally given to three patients in the month before PD-L1 tracer injection.

RESULTS

Two recently-vaccinated patients, in remission of NSCLC and receiving non-immunosuppressive cancer therapies (immunotherapy and tyrosine kinase inhibitor respectively), showed increasing PD-L1 tracer uptake in ipsilateral axillary lymph nodes. No asymmetric nodal uptake was seen in a third recently-vaccinated patient who was receiving immunosuppressive chemotherapy, or in two patients not recently-vaccinated.

CONCLUSION

Immune response to mRNA BNT162b2 vaccination may involve regulation by PD-L1 positive immune cells in local draining lymph nodes in immunocompetent patients.

TRIAL REGISTRATION

This trial was registered with the Australian New Zealand Clinical Trials Registry. Registration number ACTRN12621000171819. Date of Trial Registration 8/2/2021. Date of enrolment of 1st patient 11/4/2021. URL of trial registry record: https://www.australianclinicaltrials.gov.au/anzctr/trial/ACTRN12621000171819 .

摘要

背景

在一项针对非小细胞肺癌(NSCLC)患者的程序性细胞死亡配体-1(PD-L1)正电子发射断层显像(PET)示踪剂的0期临床试验中,三名患者在进行PD-L1成像前接受了新冠病毒疾病(COVID-19)疫苗的加强剂量注射。

方法

五名患者使用一种新型的PD-L1示踪剂进行了全身PET/CT成像,该示踪剂是通过将锆(Zr)与抗PD-L1抗体度伐鲁单抗连接而构建的。在注射PD-L1示踪剂前一个月,三名患者同时接受了肌肉注射(三角肌)的信使核糖核酸(mRNA)BNT162b2 COVID-19 mRNA疫苗加强剂量。

结果

两名近期接种疫苗的NSCLC缓解期患者,分别接受非免疫抑制性癌症治疗(分别为免疫治疗和酪氨酸激酶抑制剂),显示同侧腋窝淋巴结中PD-L1示踪剂摄取增加。在第三名接受免疫抑制化疗的近期接种疫苗患者或两名未近期接种疫苗的患者中未观察到不对称的淋巴结摄取。

结论

在有免疫能力的患者中,对mRNA BNT162b2疫苗的免疫反应可能涉及局部引流淋巴结中PD-L1阳性免疫细胞的调节。

试验注册

本试验在澳大利亚新西兰临床试验注册中心注册。注册号ACTRN12621000171819。试验注册日期2021年2月8日。第一名患者入组日期2021年4月11日。试验注册记录的网址:https://www.australianclinicaltrials.gov.au/anzctr/trial/ACTRN12621000171819

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3115/11156812/f3b3b2de36ab/41824_2024_196_Fig1_HTML.jpg

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