Wong-Arce Alejandra, Gonzalez-Ortega Omar, Romero-Maldonado Andrea, Miranda-López Arleth, García-Soto Mariano, Farfán-Castro Susan, Betancourt-Mendiola Lourdes, Teeravechyan Samaporn, Srisutthisamphan Kanjana, Comas-García Mauricio, Solís Andrade Karla I, Rosales-Mendoza Sergio
Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 6, San Luis Potosí 78210, Mexico.
Sección de Biotecnología, Centro de Investigación en Ciencias de la Salud y Biomedicina, Universidad Autónoma de San Luis Potosí, Av. Sierra Leona 550, Lomas 2a Sección, San Luis Potosí 78210, Mexico.
Pharmaceuticals (Basel). 2024 Feb 27;17(3):302. doi: 10.3390/ph17030302.
Subunit vaccines stand as a leading approach to expanding the current portfolio of vaccines to fight against COVID-19, seeking not only to lower costs but to achieve long-term immunity against variants of concern and have the main attributes that could overcome the limitations of the current vaccines. Herein a chimeric protein targeting S1 and S2 epitopes, called LTp50, was designed as a convenient approach to induce humoral responses against SARS-CoV-2. LTp50 was produced in recombinant using a conventional pET vector, recovering the expected antigen in the insoluble fraction. LTp50 was purified by chromatography (purity > 90%). The solubilization and refolding stages helped to obtain a stable protein amenable for vaccine formulation. LTp50 was adsorbed onto alum, resulting in a stable formulation whose immunogenic properties were assessed in BALB/c mice. Significant humoral responses against the S protein (BA.5 variant) were detected in mice subjected to three subcutaneous doses (10 µg) of the LTp50/alum formulation. This study opens the path for the vaccine formulation optimization using additional adjuvants to advance in the development of a highly effective anti-COVID-19 vaccine directed against the antigenic regions of the S protein, which are less prone to mutations.
亚单位疫苗是扩大当前抗击新冠病毒疫苗组合的主要方法,不仅旨在降低成本,还力求实现对关注变体的长期免疫,并具备能够克服现有疫苗局限性的主要特性。在此,一种靶向S1和S2表位的嵌合蛋白LTp50被设计为诱导针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的体液免疫反应的简便方法。LTp50利用传统的pET载体通过重组方式生产,在不溶性部分中获得预期抗原。LTp50通过色谱法纯化(纯度>90%)。溶解和复性阶段有助于获得适合疫苗制剂的稳定蛋白。LTp50吸附于明矾上,形成一种稳定制剂,其免疫原性在BALB/c小鼠中进行评估。在接受三次皮下注射(10微克)LTp50/明矾制剂的小鼠中检测到针对S蛋白(BA.5变体)的显著体液免疫反应。本研究为使用其他佐剂优化疫苗制剂开辟了道路,以推动开发针对S蛋白抗原区域、不易发生突变的高效抗新冠病毒疫苗。