Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.
Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.
Virology. 2022 Oct;575:83-90. doi: 10.1016/j.virol.2022.08.010. Epub 2022 Sep 2.
Multisystem Inflammatory Syndrome in Children (MIS-C), a post infectious complication of SARS CoV-2 infection, shares enough features with Kawasaki Disease (KD) that some have hypothesized cross-coronavirus (CoV) immunity may explain the shared pathology. Recent studies have shown that humoral cross-reactivity of the CoVs, particularly of OC43, is focused on the S2 region of the Spike protein. Due to efforts utilizing CoV S2 regions to produce a cross-CoV vaccine, we wished to assess SARS-CoV-2 S2 reactivity in children with KD and assess if cardiac involvement in KD correlated with S2 CoV antibody targeting. The presence of cross-reactivity does not distinguish KD from febrile controls and does not correlate with cardiac involvement in KD. These findings support that, in relation to cardiac vascular inflammation, vaccines targeting the S2 region appear to be a safe approach, but there is disparity in the ability of CoV species to raise cross-reactive S2 targeted antibodies.
儿童多系统炎症综合征(MIS-C)是 SARS-CoV-2 感染后的一种感染后并发症,与川崎病(KD)有足够的相似特征,因此有人假设冠状病毒(CoV)交叉免疫可能解释了共同的发病机制。最近的研究表明,CoVs 的体液交叉反应,特别是 OC43,主要集中在 Spike 蛋白的 S2 区域。由于利用 CoV S2 区域生产交叉 CoV 疫苗的努力,我们希望评估 KD 患儿中 SARS-CoV-2 S2 的反应性,并评估 KD 中的心脏受累是否与 S2 CoV 抗体靶向相关。交叉反应的存在并不能将 KD 与发热对照组区分开来,也与 KD 中的心脏受累无关。这些发现支持这样的观点,即就心脏血管炎症而言,针对 S2 区域的疫苗似乎是一种安全的方法,但不同的 CoV 物种在产生交叉反应性 S2 靶向抗体的能力上存在差异。