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  5. Intravaginal immunization using the recombinant HIV-1 clade-C trimeric envelope glycoprotein CN54gp140 formulated within lyophilized solid dosage forms
 
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Intravaginal immunization using the recombinant HIV-1 clade-C trimeric envelope glycoprotein CN54gp140 formulated within lyophilized solid dosage forms
File(s)
1-s2.0-S0264410X11005445-main.pdf (430.96 KB)
Published version
Author(s)
Donnelly, L
Curran, RM
Tregoning, JS
McKay, PF
Cole, T
more
Type
Journal Article
Abstract
Vaccine-mediated prevention of primary HIV-1 infection at the heterosexual mucosal portal of entry may be facilitated by highly optimised formulations or drug delivery devices for intravaginal (i.vag) immunization. Previously we described hydroxyethylcellulose (HEC)-based rheologically structured gel vehicles (RSVs) for vaginal immunization of an HIV-1 vaccine candidate, a soluble recombinant trimeric HIV-1 clade-C envelope glycoprotein designated CN54gp140. Here we investigated the efficacy of lyophilized solid dosage formulations (LSDFs) for prolonging antigen stability and as i.vag delivery modalities. LSDFs were designed and developed that upon i.vag administration they would reconstitute with the imbibing of vaginal fluid to mucoadhesive, site-retentive semi-solids. Mice were immunized with lyophilized equivalents of (i) RSVs, (ii) modified versions of the RSVs more suited to lyophilization (sodium carboxymethyl cellulose (NaCMC)-based gels) and (iii) Carbopol® gel, all containing CN54gp140. NaCMC-based LSDFs provided significantly enhanced antigen stability compared to aqueous-based RSVs. Rheological analysis indicated the NaCMC-based LSDFs would offer enhanced vaginal retention in woman compared to more conventional vaginal gel formulations. All LSDFs were well tolerated in the mouse model. Following i.vag administration, all LSDFs boosted systemic CN54gp140-specific antibody responses in sub-cutaneously primed mice. Induction of CN54gp140-specific antibody responses in the female genital tract was evident. Of all the LSDFs the fastest releasing which was lyophilized Carbopol® gel elicited immune responses comparable to buffer instillation of antigen suggesting that rather than slower sustained release, initial high burst release from the LSDFs may suffice. The boosting of specific immune responses upon i.vag administration indicates that LSDFs are viable mucosal vaccine delivery modalities promoting antigen stability and facilitating intimate exposure of CN54gp140 to the mucosal-associated lymphoid tissue of the female genital tract.
Date Issued
2011-04-21
Date Acceptance
2011-04-07
Citation
Vaccine, 2011, 29 (27), pp.4512-4520
URI
http://hdl.handle.net/10044/1/32870
DOI
https://www.dx.doi.org/10.1016/j.vaccine.2011.04.023
ISSN
1873-2518
Publisher
Elsevier
Start Page
4512
End Page
4520
Journal / Book Title
Vaccine
Volume
29
Issue
27
Copyright Statement
© 2011 Elsevier Ltd. Made available under a CC BY license.
License URL
http://creativecommons.org/licenses/by/4.0/
Subjects
Science & Technology
Life Sciences & Biomedicine
Immunology
Medicine, Research & Experimental
Research & Experimental Medicine
IMMUNOLOGY
MEDICINE, RESEARCH & EXPERIMENTAL
Intravaginal delivery
Mucosal vaccination
HIV-1
Lyophilized solid dosage formulations
FEMALE GENITAL-TRACT
IMMUNODEFICIENCY-VIRUS
VAGINAL IMMUNIZATION
ANTIBODY-RESPONSES
INFECTION
TYPE-1
TRANSMISSION
SECRETIONS
INDUCTION
VACCINE
AIDS Vaccines
Acrylic Resins
Administration, Intravaginal
Animals
Chemistry, Pharmaceutical
Female
Freeze Drying
Gels
HIV Antibodies
HIV Infections
Humans
Immunity, Mucosal
Immunization
Mice
Polyvinyls
Rheology
Starch
Vaccines, Synthetic
env Gene Products, Human Immunodeficiency Virus
Virology
06 Biological Sciences
07 Agricultural And Veterinary Sciences
11 Medical And Health Sciences
Publication Status
Published
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