Present Scenario of M-Cell Targeting Ligands for Oral Mucosal Immunization.
M cell
MALT
Oral mucosal immunization
Peyer’s patches
gastrointestinal
gut-associated lymphoid tissues
Journal
Current drug targets
ISSN: 1873-5592
Titre abrégé: Curr Drug Targets
Pays: United Arab Emirates
ID NLM: 100960531
Informations de publication
Date de publication:
2020
2020
Historique:
received:
18
12
2019
revised:
18
04
2020
accepted:
23
04
2020
pubmed:
10
6
2020
medline:
8
10
2021
entrez:
10
6
2020
Statut:
ppublish
Résumé
The immune system plays an important role in the prevention of infection and forms the first line of defense against pathogen attack. Delivering of antigen through mucosal route may elicit mucosal immune system as the mucosal surface is the most common site of pathogen entry. Mucosal immune system will be capable to counter pathogen at mucosal surface. Oral mucosal immunization opens the ways to deliver antigens at gut-associated lymphoid tissue. This can elicit both local and systemic immune response. Mucosal vaccines are economical, highly accessible, non parenteral delivery and capacity to produce mass immunization at the time of pandemics. To deliver antigens on the mucosal surface of the gastrointestinal tract, the immune system relies on specialized epithelial cell i.e. Microfold (M)-cell. An approach to exploit the targeting specific receptors on M-cell for entry of antigens has made a breakthrough in vaccine development. In this review, various strategies have been discussed for the possible entry of antigens through M-cells and an approach to increase the uptake and efficacy of vaccines for oral mucosal immunization.
Identifiants
pubmed: 32516099
pii: CDT-EPUB-107201
doi: 10.2174/1389450121666200609113252
doi:
Substances chimiques
Immunoglobulin A, Secretory
0
Ligands
0
Vaccines
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1276-1284Informations de copyright
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