AI Article Synopsis

  • Researchers aimed to create a safer and more effective vaccine for pneumococcal respiratory infections by integrating knowledge about common antigens and improving delivery systems across the mucosal barrier.
  • They developed a nasal vaccine using pneumococcal surface protein A (PspA) combined with a nontoxic nanogel (cCHP) for effective antigen delivery.
  • Testing on mice showed that this vaccine provided strong immunity, reduced bacterial colonization, and induced significant immune responses without affecting the central nervous system, indicating its potential as a safe and effective pneumococcal vaccine.

Article Abstract

To establish a safer and more effective vaccine against pneumococcal respiratory infections, current knowledge regarding the antigens common among pneumococcal strains and improvements to the system for delivering these antigens across the mucosal barrier must be integrated. We developed a pneumococcal vaccine that combines the advantages of pneumococcal surface protein A (PspA) with a nontoxic intranasal vaccine delivery system based on a nanometer-sized hydrogel (nanogel) consisting of a cationic cholesteryl group-bearing pullulan (cCHP). The efficacy of the nanogel-based PspA nasal vaccine (cCHP-PspA) was tested in murine pneumococcal airway infection models. Intranasal vaccination with cCHP-PspA provided protective immunity against lethal challenge with Streptococcus pneumoniae Xen10, reduced colonization and invasion by bacteria in the upper and lower respiratory tracts, and induced systemic and nasal mucosal Th17 responses, high levels of PspA-specific serum immunoglobulin G (IgG), and nasal and bronchial IgA antibody responses. Moreover, there was no sign of PspA delivery by nanogel to either the olfactory bulbs or the central nervous system after intranasal administration. These results demonstrate the effectiveness and safety of the nanogel-based PspA nasal vaccine system as a universal mucosal vaccine against pneumococcal respiratory infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647999PMC
http://dx.doi.org/10.1128/IAI.00240-13DOI Listing

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