Utke Katrin, Kock Holger, Schuetze Heike, Bergmann Sven M, Lorenzen Niels, Einer-Jensen Katja, Köllner Bernd, Dalmo Roy A, Vesely Tomas, Ototake Mitsuru, Fischer Uwe
Friedrich-Loeffler-Institute, Federal Research Institute for Animal Health, D-17493 Greifswald-Insel Riems, Germany.
Dev Comp Immunol. 2008;32(3):239-52. doi: 10.1016/j.dci.2007.05.010. Epub 2007 Jun 26.
To identify viral proteins that induce cell-mediated cytotoxicity (CMC) against viral hemorrhagic septicemia virus (VHSV)-infected cells, rainbow trout were immunized with DNA vectors encoding the glycoprotein G or the nucleocapsid protein N of VHSV. The G protein was a more potent trigger of cytotoxic cells than the N protein. Peripheral blood leukocytes (PBL) isolated from trout immunized against the G protein killed both VHSV-infected MHC class I matched (RTG-2) and VHSV-infected xenogeneic (EPC) target cells, suggesting the involvement of both cytotoxic T lymphocytes (CTL) and NK cells, respectively. In contrast, PBL from trout that were immunized against the N protein only killed VHSV-infected RTG-2 cells, indicating that this protein only elicits a CTL response. Further, a significant killing capacity of these PBL was only observed during summer months. PBL from fish that were immunized against the VHSV G protein significantly killed VHSV-infected but not infectious hematopoietic necrosis virus (IHNV)-infected targets indicating antigen specificity. Thus, this is the first report on cytotoxic immune responses after DNA vaccination in fish. Furthermore, cells isolated from the inflamed site of DNA injection were stained and transferred to isogeneic DNA-vaccinated recipients. Most of the stained donor leukocytes accumulated at the recipients' DNA injection site showing, for the first time, leukocyte homing in fish. Transferred donor leukocytes mainly migrated to the homologous vaccine injection site rather than to injection sites of heterologous vaccines, suggesting the antigen specificity of homing. By demonstrating CMC responses to distinct viral proteins and homing in rainbow trout, these results substantially contribute to the understanding of the teleost immune system.
为了鉴定能诱导针对感染病毒性出血性败血症病毒(VHSV)细胞的细胞介导细胞毒性(CMC)的病毒蛋白,用编码VHSV糖蛋白G或核衣壳蛋白N的DNA载体免疫虹鳟。与核衣壳蛋白N相比,糖蛋白G是细胞毒性细胞更有效的触发因子。从免疫糖蛋白G的鳟鱼中分离出的外周血白细胞(PBL)杀死了感染VHSV的I类主要组织相容性复合体匹配细胞(RTG-2)和感染VHSV的异种细胞(EPC)靶细胞,这分别表明细胞毒性T淋巴细胞(CTL)和自然杀伤细胞(NK细胞)均参与其中。相比之下,仅免疫核衣壳蛋白N的鳟鱼的PBL仅杀死感染VHSV的RTG-2细胞,这表明该蛋白仅引发CTL反应。此外,仅在夏季观察到这些PBL具有显著杀伤能力。免疫VHSV糖蛋白G的鱼的PBL能显著杀死感染VHSV但未感染传染性造血坏死病毒(IHNV)的靶细胞,表明具有抗原特异性。因此,这是关于鱼类DNA疫苗接种后细胞毒性免疫反应的首次报道。此外,对从DNA注射炎症部位分离的细胞进行染色,并将其转移至同基因DNA疫苗接种的受体。大多数染色的供体白细胞聚集在受体的DNA注射部位首次显示了鱼类中的白细胞归巢现象。转移的供体白细胞主要迁移至同源疫苗注射部位而非异源疫苗注射部位,表明归巢具有抗原特异性。通过证明虹鳟对不同病毒蛋白产生的CMC反应和归巢现象,这些结果极大地有助于理解硬骨鱼免疫系统。