Article

Nasal and Vaginal Vaccinations Have Differential Effects on Antibody Responses in Vaginal and Cervical Secretions in Humans

Departments of Medical Microbiology and Immunology, Göteborg University, Göteborg, Sweden.
Infection and Immunity (impact factor: 4.16). 01/2002; DOI:10.1128/IAI.69.12.7481-7486.2001
Source: PubMed Central

ABSTRACT Sexually transmitted diseases are a major health problem worldwide, but there is still a lack of knowledge about how to induce an optimal immune response in the genital tract of humans. In this study we vaccinated 21 volunteers nasally or vaginally with the model mucosal antigen cholera toxin B subunit and determined the level of specific immunoglobulin A (IgA) and IgG antibodies in vaginal and cervical secretions as well as in serum. To assess the hormonal influence on the induction of antibody responses after vaginal vaccination, we administered the vaccine either independently of the stage in the menstrual cycle or on days 10 and 24 in the cycle in different groups of subjects. Vaginal and nasal vaccinations both resulted in significant IgA and IgG anti-cholera toxin B subunit responses in serum in the majority of the volunteers in the various vaccination groups. Only vaginal vaccination given on days 10 and 24 in the cycle induced strong specific antibody responses in the cervix with 58-fold IgA and 16-fold IgG increases. In contrast, modest responses were seen after nasal vaccination and in the other vaginally vaccinated group. Nasal vaccination was superior in inducing a specific IgA response in vaginal secretions, giving a 35-fold increase, while vaginal vaccination induced only a 5-fold IgA increase. We conclude that a combination of nasal and vaginal vaccination might be the best vaccination strategy for inducing protective antibody responses in both cervical and vaginal secretions, provided that the vaginal vaccination is given on optimal time points in the cycle.

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Keywords

21 volunteers nasally
 
5-fold IgA increase
 
58-fold IgA
 
antibody responses
 
genital tract
 
IgG anti-cholera toxin B subunit responses
 
IgG antibodies
 
inducing protective antibody responses
 
major health problem
 
model mucosal antigen cholera toxin B subunit
 
Nasal vaccination
 
nasal vaccinations
 
optimal immune response
 
optimal time points
 
significant IgA
 
specific IgA response
 
specific immunoglobulin
 
vaginal vaccination
 
vaginal vaccination induced
 
various vaccination groups