Gannavaram Sreenivas, Dey Ranadhir, Avishek Kumar, Selvapandiyan Angamuthu, Salotra Poonam, Nakhasi Hira L
Division of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, Food and Drug Administration , Bethesda, MD , USA.
National Institute of Pathology, Indian Council of Medical Research , New Delhi , India.
Front Immunol. 2014 May 23;5:241. doi: 10.3389/fimmu.2014.00241. eCollection 2014.
Despite intense efforts there is no safe and efficacious vaccine against visceral leishmaniasis, which is fatal and endemic in many tropical countries. A major shortcoming in the vaccine development against blood-borne parasitic agents such as Leishmania is the inadequate predictive power of the early immune responses mounted in the host against the experimental vaccines. Often immune correlates derived from in-bred animal models do not yield immune markers of protection that can be readily extrapolated to humans. The limited efficacy of vaccines based on DNA, subunit, heat killed parasites has led to the realization that acquisition of durable immunity against the protozoan parasites requires a controlled infection with a live attenuated organism. Recent success of irradiated malaria parasites as a vaccine candidate further strengthens this approach to vaccination. We developed several gene deletion mutants in Leishmania donovani as potential live attenuated vaccines and reported extensively on the immunogenicity of LdCentrin1 deleted mutant in mice, hamsters, and dogs. Additional limited studies using genetically modified live attenuated Leishmania parasites as vaccine candidates have been reported. However, for the live attenuated parasite vaccines, the primary barrier against widespread use remains the absence of clear biomarkers associated with protection and safety. Recent studies in evaluation of vaccines, e.g., influenza and yellow fever vaccines, using systems biology tools demonstrated the power of such strategies in understanding the immunological mechanisms that underpin a protective phenotype. Applying similar tools in isolated human tissues such as PBMCs from healthy individuals infected with live attenuated parasites such as LdCen(-/-) in vitro followed by human microarray hybridization experiments will enable us to understand how early vaccine-induced gene expression profiles and the associated immune responses are coordinately regulated in normal individuals. In addition, comparative analysis of biomarkers in PBMCs from asymptomatic or healed visceral leishmaniasis individuals in response to vaccine candidates including live attenuated parasites may provide clues about determinants of protective immunity and be helpful in shaping the final Leishmania vaccine formulation in the clinical trials.
尽管付出了巨大努力,但仍没有针对内脏利什曼病的安全有效的疫苗,该病在许多热带国家是致命的且呈地方性流行。针对血液传播的寄生虫病原体(如利什曼原虫)开发疫苗的一个主要缺点是宿主针对实验性疫苗产生的早期免疫反应的预测能力不足。通常,从近交动物模型得出的免疫相关性并不能产生可轻易外推至人类的保护免疫标志物。基于DNA、亚单位、热灭活寄生虫的疫苗效果有限,这使人们认识到获得针对原生动物寄生虫的持久免疫力需要用减毒活生物体进行可控感染。辐照疟原虫作为候选疫苗最近取得的成功进一步强化了这种疫苗接种方法。我们在杜氏利什曼原虫中开发了几种基因缺失突变体作为潜在的减毒活疫苗,并广泛报道了LdCentrin1缺失突变体在小鼠、仓鼠和犬中的免疫原性。也有关于使用基因改造的减毒活利什曼原虫作为候选疫苗的其他有限研究报道。然而,对于减毒活寄生虫疫苗,广泛应用的主要障碍仍然是缺乏与保护和安全性相关的明确生物标志物。最近利用系统生物学工具评估疫苗(如流感疫苗和黄热病疫苗)的研究证明了此类策略在理解构成保护性表型基础的免疫机制方面的作用。在分离的人体组织(如来自体外感染减毒活寄生虫(如LdCen(-/-))的健康个体的外周血单核细胞)中应用类似工具,随后进行人类微阵列杂交实验,将使我们能够了解正常个体中早期疫苗诱导的基因表达谱以及相关免疫反应是如何协同调节的。此外,对无症状或已治愈的内脏利什曼病个体的外周血单核细胞中针对包括减毒活寄生虫在内的候选疫苗的生物标志物进行比较分析,可能会提供有关保护性免疫决定因素的线索,并有助于在临床试验中确定最终的利什曼原虫疫苗配方。