先进纳米螯合技术在灭活的严重急性呼吸综合征冠状病毒-2疫苗配方中生产的纳米佐剂:细胞因子和IgG反应的初步结果。

IF 1.5 4区 医学 Q4 IMMUNOLOGY Viral immunology Pub Date : 2023-07-01 Epub Date: 2023-07-28 DOI:10.1089/vim.2023.0001
Somayeh Kalanaky, Saideh Fakharzadeh, Pegah Karimi, Maryam Hafizi, Hamidreza Jamaati, Seyed Mehdi Hassanzadeh, Akbar Khorasani, Mehdi Mahdavi, Mohammad Hassan Nazaran
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引用次数: 0

摘要

尽管疫苗在各种传染病中取得了巨大成功,但目前大多数疫苗都不够有效,相反,临床批准的明矾佐剂无法诱导足够的免疫反应,包括提供保护的强大细胞免疫反应。在这项研究中,我们使用纳米螯合技术开发了新型纳米佐剂,以提高明矾佐剂灭活的严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)疫苗的效力。用不同剂量的佐剂疫苗制剂在2周内免疫BALB/c小鼠两次,并评估免疫反应。IFN-γ和IL-17细胞因子的分析结果证明了纳米螯合技术生产的纳米佐剂在将基于明矾的疫苗转向更强的Th1模式方面的有效性。此外,这些纳米佐剂改善了IL-2细胞因子反应,这表明了这些新制剂在诱导特异性T淋巴细胞增殖方面的功效。使用这些纳米佐剂增加了IL-10细胞因子的分泌,这可能代表更好的免疫调节作用,也可能潜在地预防免疫病理反应。此外,特异性IgG滴度分析揭示了这些纳米佐剂在改善体液免疫反应方面的效力。受体结合域(RBD)特异性IgG反应的酶联免疫吸附测定表明,所开发的新制剂诱导了针对该蛋白的强烈IgG反应。这项研究表明,先进纳米螯合技术生产的纳米结构对基于明矾的严重急性呼吸系统综合征冠状病毒2型疫苗具有强大的佐剂作用,不仅可以通过智能调节免疫系统来弥补明矾在诱导细胞免疫反应方面的弱点,还可以同时显著改善体液和细胞免疫反应。
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Nanoadjuvants Produced by Advanced Nanochelating Technology in the Inactivated-Severe Acute Respiratory Syndrome Coronavirus-2 Vaccine Formulation: Preliminary Results on Cytokines and IgG Responses.

Despite the great success of vaccines in various infectious diseases, most current vaccines are not effective enough, and on the contrary, clinically approved alum adjuvants cannot induce sufficient immune responses, including a potent cellular immune response to confer protection. In this study, we used Nanochelating Technology to develop novel nanoadjuvants to boost the potency of the alum-adjuvanted inactivated severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) vaccine. BALB/c mice were immunized twice over 2 weeks with different doses of adjuvanted-vaccine formulations and immune responses were assessed. The analysis results of IFN-γ and IL-17 cytokines demonstrated the effectiveness of the nanoadjuvants produced by the Nanochelating Technology in shifting the alum-based vaccine toward a stronger Th1 pattern. In addition, these nanoadjuvants improved IL-2 cytokine response, which shows the efficacy of these novel formulations in inducing specific T lymphocyte proliferation. Using these nanoadjuvants increased IL-10 cytokine secretion that may be representative of a better immunoregulatory impact and may also potentially prevent immunopathology responses. Moreover, specific IgG titer analysis revealed the potency of these nanoadjuvants in improving humoral immune responses. The enzyme-linked immunosorbent assay of receptor-binding domain (RBD)-specific IgG response showed that the developed novel formulations induced strong IgG responses against this protein. This study shows that the nanostructures produced by the Advanced Nanochelating Technology have potent adjuvant effects on alum-based SARS-CoV-2 vaccines to not only compensate for alum weakness in inducing the cellular immune responses by smart regulation of the immune system but also significantly improve the humoral and cellular immune responses simultaneously.

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来源期刊
Viral immunology
Viral immunology 医学-病毒学
CiteScore
3.60
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Viral Immunology delivers cutting-edge peer-reviewed research on rare, emerging, and under-studied viruses, with special focus on analyzing mutual relationships between external viruses and internal immunity. Original research, reviews, and commentaries on relevant viruses are presented in clinical, translational, and basic science articles for researchers in multiple disciplines. Viral Immunology coverage includes: Human and animal viral immunology Research and development of viral vaccines, including field trials Immunological characterization of viral components Virus-based immunological diseases, including autoimmune syndromes Pathogenic mechanisms Viral diagnostics Tumor and cancer immunology with virus as the primary factor Viral immunology methods.
期刊最新文献
Epstein-Barr Virus Antibodies and Autoimmune Diseases: A Bidirectional Mendelian Randomization Analysis. Profile of Cytokines and T Cell Subsets Transcription Factors in Cerebrospinal Fluid of Patients with Viral Encephalitis. Involvement of E3 Ubiquitin Ligases in Viral Infections of the Human Host. Memory T Cells Subpopulations in a Cohort of COVID-19 Vaccinated or Recovered Subjects. Correlation Between TWEAK Serum Level and HTLV-1 Proviral Load in HAM/TSP.
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