Buchhorn Reiner, Meyer Carlotta, Schulze-Forster Kai, Junker Juliane, Heidecke Harald
Department of Pediatrics, Caritas-Krankenhaus Bad Mergentheim, Uhlandstraße 7, 97980 Bad Mergentheim, Germany.
Praxis für Kinder- und Jugendmedizin, Kinderkardiologie und Erwachsene Mit Angeborenen Herzfehlern, Am Bahnhof 1, 74670 Forchtenberg, Germany.
Vaccines (Basel). 2021 Nov 18;9(11):1353. doi: 10.3390/vaccines9111353.
Multisystem inflammatory syndrome (MIS) is a new systemic inflammatory acute onset disease that mainly affects children (MIS-C) and, at a lesser frequency, adults (MIS-A); it typically occurs 3-6 weeks after acute SARS-CoV infection. It has been postulated and shown in adults that MIS may occur after SARS-CoV-2 vaccination (MIS-V). Our current case is one of the first published cases with a multisystem inflammatory syndrome in an 18-year-old adolescent after the SARS-CoV-2 vaccine from Pfizer/BionTech (BNT162b2), who fulfills the published level 1 criteria for a definitive disease: age < 21 years, fever > 3 consecutive days, pericardial effusion, elevated CRP/NT-BNP/Troponin T/D-dimeres, cardiac involvement, and positive SARS-CoV-2 antibodies. The disease starts 10 weeks after the second vaccination, with a fever (up to 40 °C) and was treated with amoxicillin for suspected pneumonia. The SARS CoV-2-PCR and several antigen tests were negative. With an ongoing fever, he was hospitalized 14 days later. A pericardial effusion (10 mm) was diagnosed by echocardiography. The C-reactive protein (174 mg/L), NT-BNP (280 pg/mL), and Troponin T (28 pg/mL) values were elevated. Due to highly elevated D-dimeres (>35,000 μg/L), a pulmonary embolism was excluded by thoracal computer tomography. If the boy did not improve with intravenous antibiotics, he was treated with intravenous immunoglobulins; however, the therapy was discontinued after 230 mg/kg if he developed high fever and hypotension. A further specialized clinic treated him with colchicine and ibuprofen. The MIS-V was discovered late, 4 months after the onset of the disease. As recently shown in four children with MIS-C after SARS-CoV-2 infection and a girl with Hashimoto thyroiditis after BNT162b2 vaccination, we found elevated functional autoantibodies against G-protein-coupled receptors that may be important for pathophysiology but are not conclusive for the diagnosis of MIS-C. Conclusion: We are aware that a misattribution of MIS-V as a severe complication of coronavirus vaccination can lead to increased vaccine hesitancy and blunt the global COVID-19 vaccination drive. However, the pediatric population is at a higher risk for MIS-C and a very low risk for COVID-19 mortality. The publication of such cases is very important to make doctors aware of this complication of the vaccination, so that therapy with intravenous immunoglobulins can be initiated at an early stage.
多系统炎症综合征(MIS)是一种新的系统性炎症急性起病疾病,主要影响儿童(MIS-C),较少影响成人(MIS-A);它通常在急性SARS-CoV感染后3-6周出现。在成人中已经推测并证实,MIS可能在接种SARS-CoV-2疫苗后发生(MIS-V)。我们目前的病例是首批发表的18岁青少年接种辉瑞/生物科技公司(BNT162b2)的SARS-CoV-2疫苗后出现多系统炎症综合征的病例之一,该病例符合已公布的明确疾病的1级标准:年龄<21岁、连续发热>3天、心包积液、CRP/NT-BNP/肌钙蛋白T/D-二聚体升高、心脏受累以及SARS-CoV-2抗体阳性。该疾病在第二次接种疫苗后10周开始,伴有发热(高达40°C),因疑似肺炎接受阿莫西林治疗。SARS CoV-2-PCR和多项抗原检测均为阴性。由于持续发热,14天后他住院治疗。超声心动图诊断有心包积液(10mm)。C反应蛋白(174mg/L)、NT-BNP(280pg/mL)和肌钙蛋白T(28pg/mL)值升高。由于D-二聚体高度升高(>35,000μg/L),胸部计算机断层扫描排除了肺栓塞。如果该男孩静脉使用抗生素后没有改善,则给予静脉注射免疫球蛋白治疗;然而,如果他出现高热和低血压,则在230mg/kg后停止治疗。另一家专科诊所用秋水仙碱和布洛芬对他进行治疗。MIS-V在疾病发作4个月后才被发现。正如最近在4例SARS-CoV-2感染后患有MIS-C的儿童和1例接种BNT162b2疫苗后患有桥本甲状腺炎的女孩中所显示的那样,我们发现针对G蛋白偶联受体的功能性自身抗体升高,这可能对病理生理学很重要,但对MIS-C的诊断尚无定论。结论:我们意识到,将MIS-V错误归因于冠状病毒疫苗的严重并发症可能会导致疫苗犹豫增加,并削弱全球COVID-19疫苗接种运动。然而,儿科人群患MIS-C的风险较高,而患COVID-19死亡的风险非常低。公布此类病例对于让医生了解这种疫苗接种并发症非常重要,以便能够早期开始静脉注射免疫球蛋白治疗。