Mukbel Rami M, Khasharmeh Rehab H, Hijjawi Nawal S, Khalifeh Mohammed S, Hatmal Ma'mon M, McDowell Mary Ann
Department of Basic Veterinary Medical Science, Faculty of Veterinary Medicine, Jordan University of Science and Technology, P.O. Box 3030, Irbid, 22110, Jordan.
Department of Medical Laboratory Sciences, Faculty of Allied Health Sciences, The Hashemite University, PO Box 150459, Zarqa, 13115, Jordan.
Parasitol Res. 2016 Sep;115(9):3345-55. doi: 10.1007/s00436-016-5094-2. Epub 2016 May 10.
Phlebotomine sand flies are the known vectors of Leishmania parasites. New approaches in vaccination against Leishmania have investigated the possibility of integrating Phlebotomus papatasi salivary proteins to enhance the immune response and protect against the transmission of the infection. The aim of the present study was to screen human immune responses to wild sand fly saliva and evaluate immunogenic salivary proteins. Blood samples were collected from donors in control and sand fly infested areas. Antibodies specific for sand fly antigens in donor plasma were probed using immunoblotting. In addition, recall proliferation capability of peripheral blood mononuclear cells (PBMC) was tested after sand fly salivary homogenates stimulation. The significant immunogenic salivary proteins (SPs) identified by immunoblotting were SP28, SP32, and SP36. A specific proliferative response of PBMC after stimulation with sand fly salivary homogenates was evident in donors that have antibody responses against sand fly salivary proteins. Individuals with antibody recognition to a higher number of salivary proteins (i.e., 3 or more SP bands) showed lower PBMC proliferative responses after in vitro stimulation with salivary gland homogenates (SGH) only in the sand fly infested, leishmaniasis free area. Interestingly, the presence of a humoral immune response to many SP antigens inversely correlates with a strong cell-mediated immune response (CMI). It was also noticed that some other heavily expressed antigens, in sand fly salivary homogenate, lack or have weak humoral immune reactivity in exposed individuals. Therefore, considering these antigens alone as CMI activators, without including the immunodominant humoral immune response proteins, needs future investigation.
白蛉是已知的利什曼原虫寄生虫的传播媒介。针对利什曼原虫的疫苗接种新方法研究了整合巴氏白蛉唾液蛋白以增强免疫反应并预防感染传播的可能性。本研究的目的是筛选人类对野生白蛉唾液的免疫反应并评估具有免疫原性的唾液蛋白。从对照地区和白蛉出没地区的献血者采集血样。使用免疫印迹法检测献血者血浆中对白蛉抗原的特异性抗体。此外,在白蛉唾液匀浆刺激后测试外周血单核细胞(PBMC)的回忆增殖能力。通过免疫印迹法鉴定出的重要免疫原性唾液蛋白(SPs)为SP28、SP32和SP36。在对白蛉唾液蛋白有抗体反应的献血者中,白蛉唾液匀浆刺激后PBMC出现明显的特异性增殖反应。仅在白蛉出没但无利什曼病的地区,对较多唾液蛋白(即3条或更多SP条带)有抗体识别的个体,在体外经唾液腺匀浆(SGH)刺激后PBMC增殖反应较低。有趣的是,对许多SP抗原的体液免疫反应的存在与强大的细胞介导免疫反应(CMI)呈负相关。还注意到,在白蛉唾液匀浆中一些其他高表达的抗原,在暴露个体中缺乏或具有较弱的体液免疫反应性。因此,仅将这些抗原视为CMI激活剂,而不包括免疫显性体液免疫反应蛋白,这需要未来进一步研究。