2000
DOI: 10.1016/s0168-3659(99)00231-x
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Oral vaccine delivery

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Cited by 83 publications
(30 citation statements)
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“…So far, some of conventional colloidal drug-delivery systems, such as liposomes and nanoparticles, have been developed and tested for PPD. [1][2][3] However, the bioavailability of peptide after oral administration is usually low due to instability and poor absorption of proteins in the gastrointestinal tract. One possible way to improve the gastrointestinal uptake of peptides is to encapsulate them in colloidal nanoparticles that can protect the peptide from being degraded in the gastrointestinal tract and facilitate their transportation into systemic circulation.…”
Section: Introductionmentioning
confidence: 99%
“…So far, some of conventional colloidal drug-delivery systems, such as liposomes and nanoparticles, have been developed and tested for PPD. [1][2][3] However, the bioavailability of peptide after oral administration is usually low due to instability and poor absorption of proteins in the gastrointestinal tract. One possible way to improve the gastrointestinal uptake of peptides is to encapsulate them in colloidal nanoparticles that can protect the peptide from being degraded in the gastrointestinal tract and facilitate their transportation into systemic circulation.…”
Section: Introductionmentioning
confidence: 99%
“…29,30 Interaction with pathogens or antigens can produce the IgA secretion as an antibody response. 31 Intracellular antigens, can be produced by invading viruses that replicate within the host cell, or derive from cytoplasmic bacteria, while the extracellular antigens include bacteria, parasites, and toxins in the tissues. Intracellular antigens are generally processed in the host cells, coupled to a major histocompatibility complex-I (MHC-I), a cell surface molecule, and transported to the cell surface.…”
Section: Respiratory Epithelial Cellsmentioning
confidence: 99%
“…This may be accompanied by the development of systemic tolerance to the fed antigen and thus a serum antibody response to the antigen is not elicited. (128) Early clinical trials have shown that oral vaccines can induce a modest degree of antibody-based immune response, (63) but their capacity to completely protect against disease still remains unproven. Thus, investment in oral vaccines will only succeed with continued efforts to design better delivery vehicles and to understand the mechanism of action of these formulations.…”
Section: Measlesmentioning
confidence: 99%