Joshi Rushika, Sheth Devang, Beladiya Jayesh, Patel Chirag, Solanki Nilay, Dalal Mittal, Kyada Ashish, Patel Sandip B
Department of Pharmacology, L.M. College of Pharmacy, Navrangpura, Ahmedabad, 380009, Gujarat, India.
Department of Pharmacology, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, CHARUSAT Campus, Changa, Petlad, Anand, Gujarat, 388421, India.
Curr Drug Discov Technol. 2025;22(3):e070624230860. doi: 10.2174/0115701638285518240601075811.
In underdeveloped nations, tuberculosis (TB) continues to be a major source of morbidity and mortality. The currently available vaccine against tuberculosis in endemic areas is mainly ineffective, which triggers the need for a clinically effective vaccine against tuberculosis. In the present review, we emphasized the impact of genetic variations in the BCG strains, which influence the efficacy of BCG vaccines. We also discussed the current status of BCG vaccines and their potential mechanisms on the modulation of B cells and, thereby, humoral immunity, which trigger immune responses against various intracellular pathogens. Further, we also elaborated upon the pre-clinical and clinical studies demonstrating the efficacy and safety of the vaccines. Moreover, we also presented the putative novel targets such as polysaccharide-induced antibodies for the protection against Mtb, PGRS domain as an important target for Humoral immunity, HLA-E pathway-Target strategy for new TB vaccine, Coronin-1a - Novel player for Mycobacterial survival, IRGM, IFN-I3, an autophagy inducer with Irgm1 serving as a core part in the Tuberculosis vaccine development.
在欠发达国家,结核病仍然是发病和死亡的主要原因。流行地区目前可用的抗结核疫苗主要无效,这引发了对临床有效的抗结核疫苗的需求。在本综述中,我们强调了卡介苗菌株基因变异的影响,这些变异会影响卡介苗的效力。我们还讨论了卡介苗的现状及其调节B细胞从而影响体液免疫的潜在机制,体液免疫可引发针对各种细胞内病原体的免疫反应。此外,我们还阐述了证明疫苗有效性和安全性的临床前和临床研究。此外,我们还提出了一些假定的新靶点,如用于预防结核分枝杆菌的多糖诱导抗体、作为体液免疫重要靶点的PGRS结构域、新型结核疫苗的HLA-E途径靶向策略、作为分枝杆菌生存新角色的冠蛋白-1a、IRGM、IFN-I3,一种自噬诱导剂,Irgm1在结核病疫苗开发中作为核心部分。