Townsend Rebecca L, Moritz Erin D, Fialkow Lawrence B, Berardi Victor, Stramer Susan L
Scientific Support Office, American Red Cross, Gaithersburg, Maryland.
Transfusion. 2014 Nov;54(11):2828-32. doi: 10.1111/trf.12675. Epub 2014 Apr 17.
Anaplasma phagocytophilum (AP), a tick-borne obligate intracellular bacterium, causes human granulocytic anaplasmosis (HGA) and has been implicated in seven transfusion-transmitted (TT)-HGA cases associated with red blood cells (RBCs). Here we report the first probable case of TT-HGA involving leukoreduced platelets (PLTs).
A hospitalized male received 25 blood components (November 2012) before his death from trauma. Hospital testing confirmed HGA by peripheral blood smears; samples were also sent to IMUGEN, Inc. (Norwood, MA), for AP-polymerase chain reaction (PCR) and AP-immunoglobulin (Ig)M and IgG enzyme immunoassay. All 12 potentially transmitting donors provided follow-up samples.
Recipient smears progressed from negative to predominantly positive 16 days posttransfusion; hospital-performed AP-PCR was positive on Day 22. IMUGEN sample testing was PCR positive and IgM and IgG negative 14 to 23 days posttransfusion. The recipient had no known AP risk factors. One of 12 donors of RBCs or PLTs (leukoreduced 5-day-old PLTs) provided six follow-up samples; all were strongly IgG positive and IgM negative; one was PCR-positive. The IgG-positive donor was a 52-year-old female from Hudson Valley, New York, an area endemic for AP. She reported tick bites in September to October 2012 with no travel outside New York. The donor remained asymptomatic and received no treatment. The cocomponent PLT unit was transfused to a 78-year-old male who died of causes unrelated to AP.
This eighth case of probable TT-HGA indicates that leukoreduced PLTs may be infectious. An antibody- and PCR-positive donor having prior tick exposure living in an endemic area was identified. PCR positivity and elevated IgG levels, which continue to exceed the assay's detectible range even in the absence of IgM, indicate active donor infection.
嗜吞噬细胞无形体(AP)是一种蜱传播的专性细胞内细菌,可引起人类粒细胞无形体病(HGA),并且已有7例与红细胞(RBC)相关的输血传播(TT)-HGA病例。在此,我们报告首例可能由白细胞滤除血小板(PLT)引起的TT-HGA病例。
一名住院男性在因创伤死亡前接受了25个血液成分(2012年11月)。医院检测通过外周血涂片确诊为HGA;样本还被送往IMUGEN公司(马萨诸塞州诺伍德)进行AP聚合酶链反应(PCR)以及AP免疫球蛋白(Ig)M和IgG酶免疫测定。所有12名可能具有传播性的献血者均提供了随访样本。
受血者的涂片在输血后16天从阴性进展为主要为阳性;医院进行的AP-PCR在第22天呈阳性。IMUGEN样本检测在输血后14至23天PCR呈阳性,IgM和IgG呈阴性。受血者没有已知的AP危险因素。12名RBC或PLT献血者(白细胞滤除的5日龄PLT)中的1名提供了6份随访样本;所有样本IgG均呈强阳性,IgM呈阴性;其中1份PCR呈阳性。IgG呈阳性的献血者是一名来自纽约哈德逊河谷的52岁女性,该地区为AP流行区。她报告在2012年9月至10月间被蜱叮咬,未出过纽约。该献血者仍无症状,未接受治疗。该混合成分的PLT单位被输给了一名78岁男性,该男性死于与AP无关的原因。
这例第八例可能的TT-HGA病例表明白细胞滤除PLT可能具有传染性。确定了一名抗体和PCR呈阳性、曾有蜱暴露且居住在流行区的献血者。PCR阳性以及IgG水平升高,即使在没有IgM的情况下仍持续超过检测范围,表明献血者存在活动性感染。