Institute of Immunology and Infection Research, Ashworth Laboratories, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.
PLoS Pathog. 2013 Aug;9(8):e1003492. doi: 10.1371/journal.ppat.1003492. Epub 2013 Aug 15.
Gastrointestinal nematode parasites infect over 1 billion humans, with little evidence for generation of sterilising immunity. These helminths are highly adapted to their mammalian host, following a developmental program through successive niches, while effectively down-modulating host immune responsiveness. Larvae of Heligmosomoides polygyrus, for example, encyst in the intestinal submucosa, before emerging as adult worms into the duodenal lumen. Adults release immunomodulatory excretory-secretory (ES) products, but mice immunised with adult H. polygyrus ES become fully immune to challenge infection. ES products of the intestinal wall 4th stage (L4) larvae are similarly important in host-parasite interactions, as they readily generate sterile immunity against infection, while released material from the egg stage is ineffective. Proteomic analyses of L4 ES identifies protective antigen targets as well as potential tissue-phase immunomodulatory molecules, using as comparators the adult ES proteome and a profile of H. polygyrus egg-released material. While 135 proteins are shared between L4 and adult ES, 72 are L4 ES-specific; L4-specific proteins correspond to those whose transcription is restricted to larval stages, while shared proteins are generally transcribed by all life cycle forms. Two protein families are more heavily represented in the L4 secretome, the Sushi domain, associated with complement regulation, and the ShK/SXC domain related to a toxin interfering with T cell signalling. Both adult and L4 ES contain extensive but distinct arrays of Venom allergen/Ancylostoma secreted protein-Like (VAL) members, with acetylcholinesterases (ACEs) and apyrase APY-3 particularly abundant in L4 ES. Serum antibodies from mice vaccinated with L4 and adult ES react strongly to the VAL-1 protein and to ACE-1, indicating that these two antigens represent major vaccine targets for this intestinal nematode. We have thus defined an extensive and novel repertoire of H. polygyrus proteins closely implicated in immune modulation and protective immunity.
肠道线虫寄生虫感染超过 10 亿人,但几乎没有产生绝育免疫的证据。这些蠕虫高度适应其哺乳动物宿主,遵循一个在连续小生境中发育的程序,同时有效地下调宿主免疫反应。例如,旋毛虫幼虫在肠黏膜下囊封,然后作为成虫进入十二指肠腔。成虫释放免疫调节排泄-分泌(ES)产物,但用旋毛虫成虫 ES 免疫的小鼠对挑战感染完全免疫。肠道壁第 4 期(L4)幼虫的 ES 产物在宿主-寄生虫相互作用中同样重要,因为它们容易产生针对感染的无菌免疫,而从卵期释放的物质则无效。使用成虫 ES 蛋白质组和旋毛虫卵释放物质的图谱作为比较,对 L4 ES 的蛋白质组分析确定了保护性抗原靶标以及潜在的组织相免疫调节分子。L4 ES 中有 135 种蛋白质与成虫 ES 共有,72 种蛋白质是 L4 ES 特异性的;L4 特异性蛋白质对应于那些转录仅限于幼虫阶段的蛋白质,而共有蛋白质通常由所有生命周期形式转录。两个蛋白质家族在 L4 分泌组中更为丰富,即与补体调节相关的 Sushi 结构域和与干扰 T 细胞信号的毒素相关的 ShK/SXC 结构域。成虫和 L4 ES 都包含广泛但不同的毒液过敏原/Ancylostoma 分泌蛋白样(VAL)成员阵列,其中乙酰胆碱酯酶(ACE)和 apyrase APY-3 在 L4 ES 中特别丰富。用 L4 和成虫 ES 疫苗接种的小鼠血清抗体强烈反应到 VAL-1 蛋白和 ACE-1,表明这两种抗原代表这种肠道线虫的主要疫苗靶标。因此,我们定义了一个广泛而新颖的旋毛虫蛋白 repertoire,这些蛋白与免疫调节和保护性免疫密切相关。