Friedrich Sarah-Kim, Schmitz Rosa, Bergerhausen Michael, Lang Judith, Cham Lamin B, Duhan Vikas, Häussinger Dieter, Hardt Cornelia, Addo Marylyn, Prinz Marco, Asano Kenichi, Lang Philipp Alexander, Lang Karl Sebastian
Institute of Immunology, University of Duisburg-Essen, Hufelandstrasse 55, 45147 Essen, Germany.
Clinic of Gastroenterology, Hepatology and Infectious Diseases, Heinrich-Heine-University, Moorenstrasse 5, 40225 Düsseldorf, Germany.
Vaccines (Basel). 2020 Mar 23;8(1):142. doi: 10.3390/vaccines8010142.
Ebola virus epidemics can be effectively limited by the VSV-EBOV vaccine (Ervebo) due to its rapid protection abilities; however, side effects prevent the broad use of VSV-EBOV as vaccine. Mechanisms explaining the efficient immune activation after single injection with the VSV-EBOV vaccine remain mainly unknown. Here, using the clinically available VSV-EBOV vaccine (Ervebo), we show that the cell-intrinsic expression of the interferon-inhibitor in CD169 macrophages is one important factor modulating the anti-Ebola virus immune response. The absence of in CD169 macrophages led to the reduced local replication of VSV-EBOV followed by a diminished innate as well as adaptive immune response. In line, -Cre x mice showed reduced innate and adaptive immune responses against the VSV wildtype strain and died quickly after infection, suggesting that a lack of makes mice more susceptible to the side effects of the VSV vector. In conclusion, our study shows that expression in CD169 macrophages is one important surrogate marker for effective vaccination against VSV-EBOV, and probably other VSV-based vaccines also.
由于其快速的保护能力,VSV-EBOV疫苗(Ervebo)可以有效地限制埃博拉病毒的流行;然而,副作用阻碍了VSV-EBOV作为疫苗的广泛使用。单次注射VSV-EBOV疫苗后有效免疫激活的机制仍主要未知。在这里,我们使用临床可用的VSV-EBOV疫苗(Ervebo),表明CD169巨噬细胞中干扰素抑制剂的细胞内源性表达是调节抗埃博拉病毒免疫反应的一个重要因素。CD169巨噬细胞中该抑制剂的缺失导致VSV-EBOV的局部复制减少,随后先天免疫和适应性免疫反应减弱。同样,-Cre x小鼠对VSV野生型毒株的先天免疫和适应性免疫反应降低,感染后很快死亡,这表明缺乏该抑制剂会使小鼠更容易受到VSV载体副作用的影响。总之,我们的研究表明,CD169巨噬细胞中的该抑制剂表达是有效接种VSV-EBOV疫苗的一个重要替代标志物,可能对其他基于VSV的疫苗也是如此。