Department of Pathology, College of Medicine, Imam Mohammad Ibn Saud Islamic University, Riyadh, Saudi Arabia.
Department of Microbiology, SmartLab, Riyadh, Saudi Arabia.
Transfusion. 2021 May;61(5):1562-1569. doi: 10.1111/trf.16347. Epub 2021 Mar 9.
Bacterial contamination of platelet concentrates (PCs) is the predominant cause of infectious transfusion reactions. The Pathogen Inactivation Mirasol system was implemented at the King Faisal Specialist Hospital (Saudi Arabia) to reduce the risk of transfusing contaminated PCs. This pilot study evaluated the effectiveness of Mirasol against Klebsiella pneumoniae, a pathogen associated with transfusion reactions, in whole blood-derived PCs.
Whole blood (WB) units inoculated with one of six K. pneumoniae strains (five clinical isolates and ATCC-700603) at a concentration of 3-38 CFU/unit, were processed using the platelet-rich plasma (PRP) method. Each spiked PC was pooled with four unspiked units. The pooled PC was split into three Mirasol storage bags: an untreated unit (control), and two units treated with Mirasol at 26 and 32 h post-WB collection, respectively. PC samples obtained before and after Mirasol treatment were used for BacT/ALERT cultures and determination of bacteria quantification. Each experiment was repeated three independent times.
Five strains were detected prior to PC treatment (24 h post-WB spiking), while one clinical isolate was not detected. Mirasol treatment after 26 h of WB collection resulted in complete inactivation of all K. pneumoniae strains. However, treatment 32 h post-WB collection resulted in the breakthrough of one clinical isolate in two of the three replicates with ~7.8 log CFU/unit detected on day 5 of PC storage.
Delayed Mirasol treatment from 26 to 32 h post-WB collection, resulted in one breakthrough. These results highlight the importance of minimizing the time between WB collection and PI treatment.
血小板浓缩物(PCs)的细菌污染是引起感染性输血反应的主要原因。Pathogen Inactivation Mirasol 系统在 King Faisal Specialist Hospital(沙特阿拉伯)实施,以降低输注污染的 PCs 的风险。这项试点研究评估了 Mirasol 对与输血反应相关的病原体肺炎克雷伯菌在全血衍生的 PCs 中的有效性。
将浓度为 3-38 CFU/单位的六种肺炎克雷伯菌菌株(五种临床分离株和 ATCC-700603)之一接种到全血单位中,使用富含血小板的血浆(PRP)方法进行处理。每个接种的 PC 与四个未接种的单位混合。混合的 PC 分为三个 Mirasol 储存袋:一个未经处理的单位(对照)和两个分别在 WB 采集后 26 和 32 小时用 Mirasol 处理的单位。在 Mirasol 处理前后获得的 PC 样本用于 BacT/ALERT 培养和细菌定量测定。每个实验重复了三次。
在 PC 处理前(WB 接种后 24 小时)检测到五株,而一株临床分离株未检出。在 WB 采集后 26 小时进行 Mirasol 处理导致所有肺炎克雷伯菌菌株完全失活。然而,在 WB 采集后 32 小时进行处理导致在三个重复实验中的两个中,一种临床分离株突破,在 PC 储存的第 5 天检测到约 7.8 log CFU/单位。
从 WB 采集后 26 小时延迟到 32 小时进行 Mirasol 处理,导致一次突破。这些结果强调了尽可能减少 WB 采集和 PI 处理之间时间的重要性。