角鲨烯油乳化的 MPL-A 和抗 CD200/CD300a 抗体佐剂全杀灭利什曼病疫苗可提供针对唐诺瓦尼寄生虫的持久免疫力

IF 4.5 3区 医学 Q2 IMMUNOLOGY Vaccine Pub Date : 2024-09-16 DOI:10.1016/j.vaccine.2024.126373
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引用次数: 0

摘要

抗原不能诱导强大的免疫反应和持久的记忆是利什曼病预防方法不断失败的主要原因。在这里,我们确定了一种标准化的全杀利什曼病疫苗(Leishvacc)在单独或与乳化在角鲨烯油中的单磷脂 A(MPL-SE)一起使用抗 CD200 和抗 CD300a 抗体佐剂时,在恢复树突状细胞(DCs)受损的抗原呈递能力、CD4+T 细胞的效应特性以及提供对唐诺瓦尼氏利什曼病寄生虫的保护方面的潜力。在单独接种或与 MPL-SE 一起接种抗体佐剂疫苗的动物中,CD11c+ DC 针对利什曼病抗原的抗原呈递能力(以 CD80、CD86、MHC-I 和 MHC-II 表面受体以及细胞内 IL-12 为测量指标)比未接种佐剂疫苗的动物更强。我们观察到抗体/MPL-SE 佐剂疫苗接种动物的 CD4+T 细胞产生了更多的增殖和促炎细胞因子,即 IL-2、IFN-γ、IL-23 和 IL-12,这进一步表明这种方法有助于抗原激活的 CD4+T 细胞获得产生促炎细胞因子的能力。在单独接种抗体或与 MPL-SE 一起接种的动物中,CD4+ 中心记忆 T 细胞的数量和寿命都显著增加,这进一步证明了这种接种方法在诱导长期保护性免疫方面的影响。单独或与 MPL-SE 一起接种抗体佐剂疫苗的动物通过限制毒性寄生虫的生长,表现出对毒性寄生虫的良好保护,这与寄生虫血症、脾脏肿大、肝脏肿大以及肝脏肉芽肿数量的显著减少有关。我们的研究结果为一种新的内脏利什曼病免疫预防方法提供了启示,这种方法不仅符合安全标准,还能提供强大的免疫原性反应,具有控制寄生虫的显著潜力。不过,还需要进一步深入研究,以确定其诱导持久免疫的能力。
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A squalene oil emulsified MPL-A and anti-CD200/CD300a antibodies adjuvanted whole-killed Leishmania vaccine provides durable immunity against L. donovani parasites

Antigenic inefficacy to induce robust immune responses and durable memory are major causes of constantly failing prophylactic approaches in leishmaniasis. Here, we determine the potential of a standardized whole-killed Leishmania vaccine (Leishvacc) adjuvanted with anti-CD200 and anti-CD300a antibodies, either alone or with monophosphoryl lipid A (MPL-SE) emulsified in squalene oil, in restoring the compromised antigen presenting abilities of dendritic cells (DCs), effector properties of CD4+T cells and providing protection against Leishmania donovani parasites. In animals vaccinated with antibodies adjuvanted vaccines, either alone or with MPL-SE, the antigen presenting abilities of CD11c+ DCs against Leishmania antigens, measured in terms of CD80, CD86, MHC-I, and MHC-II surface receptors and intracellular IL-12 were found enhanced than non-adjuvanted vaccine. We observed more proliferative and pro-inflammatory cytokines i.e. IL-2, IFN-γ, IL-23, and IL-12 producing CD4+T cells in antibodies/MPL-SE adjuvanted vaccinated animals further suggesting that this approach helps antigen activated CD4+T cells to acquire pro-inflammatory cytokines producing abilities. In antibodies, either alone or with MPL-SE, vaccinated animals, the number of CD4+ central memory T cells and their longevity were found significantly enhanced that further evidenced the impact of this vaccination approach in inducing long term protective immunity. The animals, receiving antibodies adjuvanted vaccines, either alone or with MPL-SE, exhibited excellent protection against virulent parasites by restricting their growth, which correlated with the significantly reduced parasitemia, splenomegaly, and hepatomegaly, along with fewer numbers of liver granulomas. Our findings provide an insight to a new immunoprophylactic approach against visceral leishmaniasis, which not only satisfies the safety criteria, but also provides a robust immunogenic response with remarkable potential for parasites control. However, further in-depth investigations are needed to ascertain its ability in inducing long-lasting immunity.

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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
期刊最新文献
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