Immunization with recombinant HPV16-E7d in fusion with Flagellin as a cancer vaccine: Effect of antigen-adjuvant orientation on the immune response pattern.

IF 3.3 4区 医学 Q3 IMMUNOLOGY
Meysam Gachpazan, Ali Ahmadnia Alashti, Hamid Reza Jahantigh, Majid Moghbeli, Sobhan Faezi, Seyed Younes Hosseini, Mohammad Mahdi Eftekharian, Maryam Nasimi, Farhad Motavalli Khiavi, Alireza Rahimi, Reza Arabi Mianroodi, Mahdi Pakjoo, Morteza Taghizadeh, Maria Tempesta, Mehdi Mahdavi
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引用次数: 0

Abstract

Human papillomavirus (HPV) is the leading cause of cervical cancer worldwide. The pathogenesis of HPV is mainly dependent on its E7 and E6 proteins. Up to now, different adjuvants have been used to enhance the efficacy of the immune response against these two proteins. In this study, Flagellin (FLA) was used as adjuvant to test adjuvant activity and also see whether its orientation of attachment can affect the immune response pattern. The E7d-FLA and FLA-E7d in pET28a vector were constructed and then the recombinant proteins were expressed in E. coli BL21 (DE3) bacteria under IPTG induction. The expression of recombinant E7d-FLA and FLA-E7d proteins is confirmed by SDS-PAGE and western blot. Then, recombinant fusion proteins were purified using a nickel-nitrilotriacetic acid (Ni-NTA) column. The recombinant proteins were checked for endotoxin contamination and then quantified by Bradford. Eight-to-ten-week-old male Balb/C mice were immunized subcutaneously with 10 µg recombinant E7d-FLA, FLA-E7d and HPV16E7d vaccine on days 0, 14 and 28. In addition, PBS and FLA groups were considered as control group. Then, spleen cells were harvested to assess lymphocyte proliferation and IFN-γ, IL-4 and IL-17 cytokines. In addition, mice sera were used for specific total IgG and IgG1, IgG2a, IgG2b and IgM antibodies assessment by ELISA. The results show that E7d-FLA is more potent in the induction of lymphocyte proliferation, CTL response and specific total IgG, IgG2a and IgG2b response, while the FLA-E7d vaccine was associated with more IFN-γ, and IL-17 cytokine response. The results of this study proved the ability of FLA as an adjuvant in fusion with E7d in the induction of cellular and humoral immune responses. In addition, it also emphasizes that antigen-adjuvant orientation can affect the immune response strength and polarization against HPV E7d vaccine candidate. HIGHLIGHTS: Flagellin is attached to HPV-16 E7d at the C- or N-terminus to create E7d-FLA and FLA-E7d candidate vaccines. The E7d-FLA vaccine showed a significant increase in lymphocyte proliferation, CTL response and IgG response versus FLA-E7d vaccine. The FLA-E7d vaccine is associated with a significant increase in IFN-γ and IL-17 cytokines response versus E7d-FLA vaccine. It seems that that antigen-adjuvant orientation is an important parameter in the strength and polarization of immune response in HPV E7d vaccine candidate.

重组HPV16-E7d与鞭毛蛋白融合免疫肿瘤疫苗:抗原-佐剂取向对免疫应答模式的影响
人类乳头瘤病毒(HPV)是全球宫颈癌的主要原因。HPV的发病机制主要依赖于其E7和E6蛋白。到目前为止,已经使用了不同的佐剂来增强对这两种蛋白质的免疫反应的功效。本研究以鞭毛蛋白(Flagellin, FLA)作为佐剂,检测佐剂活性,并观察其附着方向是否会影响免疫反应模式。构建pe28a载体中的E7d-FLA和FLA-E7d,在IPTG诱导下在大肠杆菌BL21 (DE3)中表达重组蛋白。SDS-PAGE和western blot证实重组E7d-FLA和FLA-E7d蛋白的表达。然后,用镍-硝基三乙酸(Ni-NTA)柱纯化重组融合蛋白。重组蛋白进行内毒素污染检查,然后进行Bradford定量。8 ~ 10周龄雄性Balb/C小鼠分别于第0、14、28天皮下接种10µg重组E7d-FLA、FLA-E7d和HPV16E7d疫苗。PBS组和FLA组作为对照组。然后,收集脾脏细胞以评估淋巴细胞增殖和IFN-γ、IL-4和IL-17细胞因子。此外,采用ELISA法测定小鼠血清中特异性总IgG及IgG1、IgG2a、IgG2b和IgM抗体。结果表明,E7d-FLA更能诱导淋巴细胞增殖、CTL反应和特异性总IgG、IgG2a和IgG2b反应,而FLA-E7d疫苗能诱导更多的IFN-γ和IL-17细胞因子反应。本研究结果证明了FLA作为佐剂与E7d融合诱导细胞和体液免疫反应的能力。此外,还强调了抗原佐剂取向可以影响HPV E7d候选疫苗的免疫应答强度和极化。重点:鞭毛蛋白附着在HPV-16 E7d的C端或n端,产生E7d- fla和FLA-E7d候选疫苗。E7d-FLA疫苗与FLA-E7d疫苗相比,淋巴细胞增殖、CTL反应和IgG反应显著增加。与E7d-FLA疫苗相比,FLA-E7d疫苗与IFN-γ和IL-17细胞因子反应显著增加相关。抗原-佐剂取向是影响HPV E7d候选疫苗免疫应答强度和极化的重要参数。
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来源期刊
Immunologic Research
Immunologic Research 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
83
审稿时长
6-12 weeks
期刊介绍: IMMUNOLOGIC RESEARCH represents a unique medium for the presentation, interpretation, and clarification of complex scientific data. Information is presented in the form of interpretive synthesis reviews, original research articles, symposia, editorials, and theoretical essays. The scope of coverage extends to cellular immunology, immunogenetics, molecular and structural immunology, immunoregulation and autoimmunity, immunopathology, tumor immunology, host defense and microbial immunity, including viral immunology, immunohematology, mucosal immunity, complement, transplantation immunology, clinical immunology, neuroimmunology, immunoendocrinology, immunotoxicology, translational immunology, and history of immunology.
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