Alphavirus-based hepatitis C virus therapeutic vaccines: can universal helper epitopes enhance HCV-specific cytotoxic T lymphocyte responses?

Q2 Medicine
Georgia Koutsoumpli, P. Ip, Ilona Schepel, B. Hoogeboom, A. Boerma, T. Daemen
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引用次数: 3

Abstract

Background: Antigen-specific T cell immune responses play a pivotal role in resolving acute and chronic hepatitis C virus (HCV) infections. Currently, no prophylactic or therapeutic vaccines against HCV are available. We previously demonstrated the preclinical potency of therapeutic HCV vaccines based on recombinant Semliki Forest virus (SFV) replicon particles. However, clinical trials do not always meet the high expectations of preclinical studies, thus, optimization of vaccine strategies is crucial. In efforts to further increase the frequency of HCV-specific immune responses in the candidate SFV-based vaccines, the authors assessed whether inclusion of three strong, so-called universal helper T cell epitopes, and an endoplasmic reticulum localization, and retention signal (collectively termed sigHELP-KDEL cassette) could enhance HCV-specific immune responses. Methods: We included the sigHELP-KDEL cassette in two of the candidate SFV-based HCV vaccines, targeting NS3/4A and NS5A/B proteins. We characterized the new constructs in vitro for the expression and stability of the transgene-encoded proteins. Their immune efficacy with respect to HCV-specific immune responses in vivo was compared with the parental SFV vaccine expressing the corresponding HCV antigen. Further characterization of the functionality of the HCV-specific CD8+ T cells was assessed by surface and intracellular cytokine staining and flow cytometry analysis. Results: Moderate, but significantly, enhanced frequencies of antigen-specific immune responses were achieved upon lower/suboptimal dosage immunization. In optimal dosage immunization, the inclusion of the cassette did not further increase the frequencies of HCV-specific CD8+ T cells when compared with the parental vaccines and the frequencies of effector and memory populations were identical. Conclusion: We hypothesize that the additional effect of the sigHELP-KDEL cassette in SFV-based vaccines depends on the immunogenicity, nature, and stability of the target antigen expressed by the vaccine.
基于甲病毒的丙型肝炎病毒治疗性疫苗:通用辅助表位能否增强丙型肝炎病毒特异性细胞毒性T淋巴细胞反应?
背景:抗原特异性T细胞免疫反应在解决急性和慢性丙型肝炎病毒(HCV)感染中起着关键作用。目前,还没有针对丙型肝炎病毒的预防性或治疗性疫苗。我们先前证明了基于重组塞姆利基森林病毒(SFV)复制子颗粒的治疗性HCV疫苗的临床前效力。然而,临床试验并不总是满足临床前研究的高期望,因此,疫苗策略的优化至关重要。为了进一步提高候选的基于SFV的疫苗中HCV特异性免疫反应的频率,作者评估了包含三个强的、所谓的通用辅助T细胞表位、内质网定位和保留信号(统称为sigHELP-KDEL盒)是否可以增强HCV特异性免疫反应。方法:我们将sigHELP-KDEL盒纳入两种候选的基于SFV的HCV疫苗中,靶向NS3/4A和NS5A/B蛋白。我们在体外对转基因编码蛋白的表达和稳定性进行了表征。将它们在体内对HCV特异性免疫应答的免疫效力与表达相应HCV抗原的亲代SFV疫苗进行比较。通过表面和细胞内细胞因子染色和流式细胞术分析评估HCV特异性CD8+T细胞功能的进一步表征。结果:在较低/次优剂量免疫后,抗原特异性免疫反应的频率得到了适度但显著的增强。在最佳剂量免疫中,与亲代疫苗相比,盒的加入并没有进一步增加HCV特异性CD8+T细胞的频率,并且效应群体和记忆群体的频率是相同的。结论:我们假设sigHELP-KDEL盒在基于SFV的疫苗中的额外作用取决于疫苗表达的靶抗原的免疫原性、性质和稳定性。
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来源期刊
Therapeutic Advances in Vaccines and Immunotherapy
Therapeutic Advances in Vaccines and Immunotherapy Medicine-Pharmacology (medical)
CiteScore
5.10
自引率
0.00%
发文量
15
审稿时长
8 weeks
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