Mucosal IgA response to rectally administered antigen formulated in IgA-coated liposomes

Détails

ID Serval
serval:BIB_93AB8831A990
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Mucosal IgA response to rectally administered antigen formulated in IgA-coated liposomes
Périodique
Vaccine
Auteur⸱e⸱s
Zhou  F., Kraehenbuhl  J. P., Neutra  M. R.
ISSN
0264-410X (Print)
Statut éditorial
Publié
Date de publication
05/1995
Volume
13
Numéro
7
Pages
637-44
Notes
Journal Article
Research Support, U.S. Gov't, P.H.S. --- Old month value: May
Résumé
Ferritin, a soluble model antigen, was used to test whether liposomes can provide an effective delivery vehicle for mucosal immunization via the rectum, and whether the local colonic/rectal secretory immune response to antigen in liposomes can be enhanced by immunoadjuvants. The colonic/rectal IgA response to liposomal ferritin was significantly enhanced over the response to free ferritin but only when cholera toxin (CT) was present as adjuvant. The presence of IgA on the liposome surface increased the uptake of liposomes into Peyer's patch mucosa, and the local rectal/colonic immune response to ferritin about 5-fold over uncoated liposomes. These results show that (1) liposomes co-administered with immunoadjuvants can be used for mucosal immunization via the rectum. (2) Cholera toxin is an effective immunoadjuvant in the rectal/colonic mucosa. (3) IgA can enhance the local secretory immune response to antigen in liposomes, apparently by increasing liposome uptake via M cells.
Mots-clé
Adjuvants, Immunologic/*administration & dosage Administration, Rectal Animals Cholera Toxin/administration & dosage Female Ferritins/administration & dosage/immunology Immunization Immunoglobulin A, Secretory/*biosynthesis Intestinal Mucosa/*immunology Liposomes/*administration & dosage Mice Mice, Inbred BALB C
Pubmed
Web of science
Création de la notice
25/01/2008 16:05
Dernière modification de la notice
20/08/2019 15:56
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