首页> 美国卫生研究院文献>Infection and Immunity >Stimulation of T-Helper Cell Gamma Interferon and Immunoglobulin G Responses Specific for Babesia bovis Rhoptry-Associated Protein 1 (RAP-1) or a RAP-1 Protein Lacking the Carboxy-Terminal Repeat Region Is Insufficient To Provide Protective Immunity against Virulent B. bovis Challenge
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Stimulation of T-Helper Cell Gamma Interferon and Immunoglobulin G Responses Specific for Babesia bovis Rhoptry-Associated Protein 1 (RAP-1) or a RAP-1 Protein Lacking the Carboxy-Terminal Repeat Region Is Insufficient To Provide Protective Immunity against Virulent B. bovis Challenge

机译:特异针对牛津巴氏杆菌Rhoptry相关蛋白1(RAP-1)或缺少羧基末端重复区的RAP-1蛋白的T辅助细胞γ干扰素和免疫球蛋白G应答的刺激不足以提供针对强毒牛芽孢杆菌的保护性免疫。挑战

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摘要

Rhoptry-associated protein 1 (RAP-1) is a targeted vaccine antigen for Babesia bovis and Babesia bigemina infections of cattle. The 60-kDa B. bovis RAP-1 is recognized by antibodies and T lymphocytes from cattle that recovered from infection and were immune to subsequent challenge. Immunization with native or recombinant protein was reported to reduce parasitemias in challenged animals. We recently reported that the NT domain of B. bovis RAP-1 contained immunodominant T-cell epitopes, whereas the repeat-rich CT domain was less immunostimulatory for T lymphocytes from cattle immune to B. bovis. The present study was therefore designed to test the hypothesis that the NT region of RAP-1, used as a vaccine with interleukin-12 and RIBI (catalog no. R-730; RIBI Immunochem Research, Inc., Hamilton, Mont. [now Corixa, Seattle, Wash.]) adjuvant to induce a type 1 response, would prime calves for antibody and T-helper cell responses comparable to or greater than those induced by full-length RAP-1 containing the C-terminal repeats. Furthermore, a type 1 immune response to RAP-1 was hypothesized to induce protection against challenge. Following four inoculations of either recombinant full-length RAP-1 or RAP-1 NT protein, RAP-1-specific immunoglobulin G (IgG) titers, T-lymphocyte proliferation, and gamma interferon production were similar. Similar numbers of NT region peptides were recognized. However, in spite of the presence of strong RAP-1-specific IgG and CD4+-T-lymphocyte responses that were recalled upon challenge, neither antigen stimulated a protective immune response. We conclude that successful priming of calves with recombinant RAP-1 and adjuvants that elicit strong Th1 cell and IgG responses is insufficient to protect calves against virulent B. bovis challenge.
机译:Rhoptry-associated protein 1(RAP-1)是针对牛牛巴贝斯虫和大巴贝斯虫的牛的靶向疫苗抗原。牛的抗体和T淋巴细胞可识别60 kDa的牛双歧杆菌RAP-1,这些抗体和T淋巴细胞可从感染中恢复过来,并对随后的攻击免疫。据报道,用天然或重组蛋白免疫可减少感染动物的寄生虫病。最近,我们报道了牛B. RAP-1的NT结构域包含免疫占主导地位的T细胞表位,而富含重复序列的CT结构域对牛免疫牛B.的牛T淋巴细胞的免疫刺激性较低。因此,本研究旨在检验以下假设:RAP-1的NT区用作白介素12和RIBI的疫苗(目录号R-730; RIBI Immunochem Research,Inc.,汉密尔顿,蒙大拿州[现在诱导1型应答的佐剂将引发犊牛的抗体和T辅助细胞应答,这些应答与包含C末端重复序列的全长RAP-1诱导的应答相当或更高。此外,假设对RAP-1的1型免疫反应可诱导针对攻击的保护作用。重组全长RAP-1或RAP-1 NT蛋白的四次接种后,RAP-1特异性免疫球蛋白G(IgG)滴度,T淋巴细胞增殖和γ干扰素产生相似。识别出相似数目的NT区肽。然而,尽管存在强RAP-1特异性IgG和CD4 + -T淋巴细胞应答,但在攻击后均被召回,但两种抗原均未刺激保护性免疫应答。我们得出的结论是,用重组RAP-1和引发强烈Th1细胞和IgG应答的佐剂成功引发小牛不足以保护小牛免受牛B. Bovis攻击。

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