TIR-TLR7与新城疫灭活疫苗联合增强鸡细胞介导的免疫反应

S. Rashid, S. Shahsavandi, M. Ebrahimi, S. Soleimani
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摘要

引言:活疫苗和灭活疫苗被广泛用于对抗新城疫,新城疫是一种高度传染性和急性病毒感染的家禽和野生鸟类。需要更高和更长的免疫反应来改善对疾病的控制。本研究的目的是评估免疫调节蛋白TLR7(即TIR-TLR7)的保守TIR结构域作为生物佐剂在增强接种鸡对灭活ND病毒(NDV)V4株抗原的细胞介导免疫方面的潜力。方法:将新城疫病毒V4株在SPF级鸡胚中繁殖,用福尔马林灭活。在肌内给药之前,将10μg的TIRTLR7与NDV抗原混合。50只SPF鸡分为A-E组(n=10),由阴性对照、TIR-TLR7、灭活NDV抗原、TIR-TR7/灭活ND病毒抗原组成,并在增强平台中采用相同的方案。在接种疫苗后6周内每隔一周采集血样。体液反应通过使用HI试验检测特异性NDV抗体滴度来测量。用MTT法测定脾细胞培养液中淋巴细胞增殖,评价细胞介导的免疫。结果:与对照组相比,用TIR-TLR7/灭活NDV抗原免疫的所有鸡对NDV具有显著的细胞介导和HI反应(P<0.05)。在prime试验和boost试验之间没有观察到统计学上的显著差异。结论:TIR-TLR7与灭活的NDV抗原联合应用可在体液和细胞水平上产生较强的免疫应答。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancement of cell-mediated immune response in chickens by combination of TIR-TLR7 with inactivated Newcastle disease vaccine
Introduction: Live and inactivated vaccines are wildly used against Newcastle disease (ND) which is a highly contagious and acute viral infection of domestic and wild birds. A higher and prolonged immune response is required to improve the control of the disease. The aim of this study was to evaluate the potential of the conserved TIR domain of an immune regulatory protein TLR7 (i.e. TIR-TLR7) as a biological adjuvant in enhancing cell-mediated immunity in vaccinated chickens against the inactivated ND virus (NDV) V4 strain antigen. Methods: NDV V4 strain was propagated in chicken embryonated SPF eggs, tittered and then inactivated by formalin. The amount of 10 μg of TIRTLR7 was mixed with the NDV antigen before intramuscular administration. Fifty SPF chickens were divided in A-E groups (n=10), consisted of negative control, TIR-TLR7, inactivated NDV antigen, TIR-TLR7/inactivated NDV antigen in prime, and the same regimen in boost platform. The blood samples were collected at week intervals up to 6 weeks post-vaccination. Humoral response was measured by detection of specific NDV antibody titer using the HI test. The cell-mediated immunity was evaluated by measuring lymphocyte proliferation in splenocytes cell culture using MTT. Results: All immunized chickens with TIR-TLR7/inactivated NDV antigen had significant (P < 0.05) cellmediated and HI responses to NDV compared to the control groups. No statistically-significant difference was observed between the prime and boost trials. Conclusion: The results indicated that the combination of TIR-TLR7 and inactivated NDV antigen gave a strong immune response at both the humoral and the cellular levels.
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