Smit Cornelis H, Kies Christiaan L, McWilliam Hamish E G, Meeusen Els N T, Hokke Cornelis H, van Diepen Angela
Department of Parasitology, Center of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Department of Microbiology and Immunology, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
Infect Immun. 2015 Oct 12;84(1):21-33. doi: 10.1128/IAI.00954-15. Print 2016 Jan.
Schistosomiasis is a tropical disease affecting over 230 million people worldwide. Although effective drug treatment is available, reinfections are common, and development of immunity is slow. Most antibodies raised during schistosome infection are directed against glycans, some of which are thought to be protective. Developing schistosomula are considered most vulnerable to immune attack, and better understanding of local antibody responses raised against glycans expressed by this life stage might reveal possible glycan vaccine candidates for future vaccine research. We used antibody-secreting cell (ASC) probes to characterize local antiglycan antibody responses against migrating Schistosoma japonicum schistosomula in different tissues of rats. Analysis by shotgun Schistosoma glycan microarray resulted in the identification of antiglycan antibody response patterns that reflected the migratory pathway of schistosomula. Antibodies raised by skin lymph node (LN) ASC probes mainly targeted N-glycans with terminal mannose residues, Galβ1-4GlcNAc (LacNAc) and Galβ1-4(Fucα1-3)GlcNAc (LeX). Also, responses to antigenic and schistosome-specific glycosphingolipid (GSL) glycans containing highly fucosylated GalNAcβ1-4(GlcNAcβ1)n stretches that are believed to be present at the parasite's surface constitutively upon transformation were found. Antibody targets recognized by lung LN ASC probes were mainly N-glycans presenting GalNAcβ1-4GlcNAc (LDN) and GlcNAc motifs. Surprisingly, antibodies against highly antigenic multifucosylated motifs of GSL glycans were not observed in lung LN ASC probes, indicating that these antigens are not expressed in lung stage schistosomula or are not appropriately exposed to induce immune responses locally. The local antiglycan responses observed in this study highlight the stage- and tissue-specific expression of antigenic parasite glycans and provide insights into glycan targets possibly involved in resistance to S. japonicum infection.
血吸虫病是一种热带疾病,全球有超过2.3亿人受其影响。尽管有有效的药物治疗方法,但再感染很常见,而且免疫发展缓慢。血吸虫感染期间产生的大多数抗体都针对聚糖,其中一些被认为具有保护作用。发育中的血吸虫幼虫被认为最容易受到免疫攻击,更好地了解针对这个生命阶段所表达聚糖产生的局部抗体反应,可能会为未来的疫苗研究揭示潜在的聚糖疫苗候选物。我们使用抗体分泌细胞(ASC)探针来表征大鼠不同组织中针对迁移的日本血吸虫幼虫的局部抗聚糖抗体反应。通过鸟枪法血吸虫聚糖微阵列分析,确定了反映血吸虫幼虫迁移途径的抗聚糖抗体反应模式。皮肤淋巴结(LN)ASC探针产生的抗体主要靶向带有末端甘露糖残基的N-聚糖、Galβ1-4GlcNAc(乳糖胺)和Galβ1-4(Fucα1-3)GlcNAc(LeX)。此外,还发现了对含有高度岩藻糖基化的GalNAcβ1-4(GlcNAcβ1)n片段的抗原性和血吸虫特异性糖鞘脂(GSL)聚糖的反应,据信这些片段在寄生虫转化后会持续存在于其表面。肺LN ASC探针识别的抗体靶点主要是呈现GalNAcβ1-4GlcNAc(LDN)和GlcNAc基序的N-聚糖。令人惊讶的是,在肺LN ASC探针中未观察到针对GSL聚糖高度抗原性多岩藻糖基化基序的抗体,这表明这些抗原在肺期血吸虫幼虫中不表达,或者没有适当地暴露以诱导局部免疫反应。本研究中观察到的局部抗聚糖反应突出了抗原性寄生虫聚糖的阶段和组织特异性表达,并为可能参与抵抗日本血吸虫感染的聚糖靶点提供了见解。