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Synthesis and Characterization of mRNA-Loaded Poly(Beta Aminoesters) Nanoparticles for Vaccination Purposes
Published on: August 13, 2021
Abstract:
Ribosomal vaccines have been prepared from several different bacterial, fungal, and protozoan microorganisms. Most of these preparations offer a higher degree of protection than do vaccines made from the homologous whole cells, but the mode of protection is controversial. All of the reported ribosomal vaccines are contaminated with cell surface determinants. Antisera raised to ribosomal preparations are directed to innate ribosomal components as well as to surface antigens. Several hypotheses exist for the reported protection from disease: the cell surface contaminants serve as the protective moieties; ribosomes act as potent adjuvants for contaminating cell surface determinants; ribosomes innately contain antigenic determinants that cross-react with cell surface antigens; recently translated cell surface polypeptides are still attached to the ribosomal RNA in the ribosomes; ribosomes migrate from the cytoplasm of the microbe to the periphery of the cell, and ribosomal antigens are exposed on the cell surface; or ribosomes contain messenger RNA and produce microbial cell surface polypeptides in immunized individuals. A short description of the biochemical, biophysical, and structural characteristics of prokaryotic and eukaryotic ribosomes is presented, followed by a discussion of the ability of various ribosomal vaccines to protect against infectious agents.
Insights
Ribosomal vaccines offer enhanced protection against microbes, but their exact mechanism is debated. Contaminants on the ribosomes may be responsible for the protective effects observed in these vaccines.
Area of Science:
- Immunology
- Microbiology
- Biochemistry
Background:
- Ribosomal vaccines derived from bacteria, fungi, and protozoa show promise.
- These vaccines often provide superior protection compared to whole-cell vaccines.
- The precise mechanism of protection offered by ribosomal vaccines remains controversial and debated.
Purpose of the Study:
- To investigate the protective mechanisms of ribosomal vaccines.
- To explore the role of contaminants in ribosomal vaccine efficacy.
- To discuss the biochemical and structural characteristics of ribosomes in relation to vaccine potential.
Main Methods:
- Preparation of ribosomal vaccines from various microorganisms.
- Analysis of ribosomal vaccine composition, including contaminants.
- Review of existing hypotheses regarding ribosomal vaccine protection.
- Description of prokaryotic and eukaryotic ribosome characteristics.
Main Results:
- Ribosomal vaccines are consistently contaminated with cell surface determinants.
- Antisera to ribosomal preparations target both ribosomal components and surface antigens.
- Multiple hypotheses exist to explain the protective effects, involving contaminants, adjuvants, cross-reactivity, or in-situ protein synthesis.
Conclusions:
- The protective efficacy of ribosomal vaccines may be attributed to contaminating cell surface antigens.
- Ribosomes might act as adjuvants, enhancing the immune response to these contaminants.
- Further research is needed to elucidate the exact contribution of ribosomal components versus contaminants to vaccine-induced immunity.
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