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使用 Leukokit® 对粒细胞进行放射性标记,并引入密度梯度介质作为辅助材料。

Granulocyte radiolabeling using Leukokit® with introduction of a density gradient medium as ancillary material.

机构信息

Department of Nuclear Medicine, Archet Hospital, University Côte d'Azur, Nice, France -

Department of Pharmacy, Archet Hospital, University Côte d'Azur, Nice, France -

出版信息

Q J Nucl Med Mol Imaging. 2020 Sep;64(3):307-312. doi: 10.23736/S1824-4785.19.03073-5. Epub 2019 Feb 21.

Abstract

BACKGROUND

Radiolabeled white blood cells (WBCs) prepared in radiopharmacies are used to detect infectious or inflammatory sites with scintigraphy. Radiolabeling can be performed by using a disposable closed device, Leukokit®. Nevertheless, owing to the high radiosensitivity of lymphocytes, the question of eliminating lymphocytes before granulocyte radiolabeling is still a controversial step. The aim of this study was to assess a new modified Leukokit® with a protocol that allows granulocyte radiolabeling only.

METHODS

Seventy patients (male/female: 40/30, mean age: 61 years) with suspected infectious diseases underwent labeled leukocyte scintigraphy by radiolabeling with a density gradient medium in addition to Leukokit®. Compliance and quality of radiolabeling were checked according to the following criteria: visual inspection, labeling efficiency, cell viability (Trypan blue exclusion test), cell subset recovery test, lymphocyte elimination rate (granulocyte/WBC rate) and sterility test using media fills.

RESULTS

Visual inspection showed that all cell preparations were free of residual cell clumps or fibrin clots. Mean labeling efficiency was 70.4±9.4% compliant with EANM Guidelines for leukocyte labeling. The mean cell viability was 97.7±1.4% (>96%). The mean number of leucocytes injected was 116x106 ±62x106 (>50x106). The mean erythrocyte/WBC ratio was 2.1 ±0.9 (<3) and the removed lymphocyte rate was 97.4±1.6% (>90%). Finally, the three sterility tests were negative and therefore successful.

CONCLUSIONS

Purification of granulocytes with Leukokit® can safely, easily and effectively be performed using a density gradient medium. Moreover, clarification regarding the status of density gradient medium could provide support for its clinical use even if further studies are needed. Since all technical obstacles have been removed, the precautionary principle should apply and lead users to eliminate lymphocytes that are highly radiosensitive cells and whose in vivo fate is uncertain.

摘要

背景

放射性标记的白细胞(WBC)在放射药房中制备,用于通过闪烁照相术检测感染或炎症部位。放射性标记可以使用一次性封闭设备 Leukokit® 进行。然而,由于淋巴细胞的高放射敏感性,在粒细胞放射性标记之前消除淋巴细胞的问题仍然是一个有争议的步骤。本研究的目的是评估一种新的改良 Leukokit®,该试剂盒采用一种方案,仅允许粒细胞放射性标记。

方法

70 名(男/女:40/30,平均年龄:61 岁)疑似传染病患者通过密度梯度介质与 Leukokit® 联合进行标记白细胞闪烁照相术。根据以下标准检查放射性标记的符合率和质量:目视检查、标记效率、细胞活力(台盼蓝排除试验)、细胞亚群恢复试验、淋巴细胞消除率(粒细胞/WBC 率)和使用培养基填充的无菌试验。

结果

目视检查显示所有细胞制剂均无残留细胞团块或纤维蛋白凝块。平均标记效率为 70.4±9.4%,符合 EANM 白细胞标记指南。平均细胞活力为 97.7±1.4%(>96%)。注射的白细胞平均数为 116x106 ±62x106(>50x106)。红细胞/WBC 比值平均为 2.1 ±0.9(<3),去除的淋巴细胞率为 97.4±1.6%(>90%)。最后,三个无菌试验均为阴性,因此成功。

结论

使用密度梯度介质,Leukokit® 可以安全、轻松且有效地纯化粒细胞。此外,即使需要进一步的研究,澄清密度梯度介质的状况也可以为其临床应用提供支持。由于所有技术障碍都已消除,预防原则应该适用,并促使使用者消除高放射性敏感性细胞的淋巴细胞,因为其体内命运尚不确定。

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