细菌外膜
小泡
抗原
TLR2型
免疫系统
微生物学
化学
TLR4型
生物
膜
免疫学
生物化学
基因
大肠杆菌
作者
Edna George,Avijit Goswami,Tejan Lodhiya,Priyanka Padwal,Shalini Iyer,Iti Gauttam,Lakshay Sethi,Sharumathi Jeyasankar,Pallavi Raj Sharma,Ameya A. Dravid,Raju Mukherjee,Rachit Agarwal
出处
期刊:Biomaterials advances
日期:2022-06-27
卷期号:139: 213003-213003
被引量:10
标识
DOI:10.1016/j.bioadv.2022.213003
摘要
Tuberculosis (TB) is one of the most widely prevalent infectious diseases that cause significant mortality. Bacillus Calmette-Guérin (BCG), the current TB vaccine used in clinics, shows variable efficacy and has safety concerns for immunocompromised patients. There is a need to develop new and more effective TB vaccines. Outer membrane vesicles (OMVs) are vesicles released by Mycobacteria that contain several lipids and membrane proteins and act as a good source of antigens to prime immune response. However, the use of OMVs as vaccines has been hampered by their heterogeneous size and low stability. Here we report that mycobacterial OMVs can be stabilized by coating over uniform-sized 50 nm gold nanoparticles. The OMV-coated gold nanoparticles (OMV-AuNP) show enhanced uptake and activation of macrophages and dendritic cells. Proteinase K and TLR inhibitor studies demonstrated that the enhanced activation was attributed to proteins present on OMVs and was mediated primarily by TLR2 and TLR4. Mass spectrometry analysis revealed several potential membrane proteins that were common in both free OMVs and OMV-AuNP. Such strategies may open up new avenues and the utilization of novel antigens for developing TB vaccines.
科研通智能强力驱动
Strongly Powered by AbleSci AI