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Infection and Immunity, June 1999, p. 2884-2890, Vol. 67, No. 6
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Antibody Responses in the Lower Respiratory Tract and Male
Urogenital Tract in Humans after Nasal and Oral Vaccination with
Cholera Toxin B Subunit
Anna
Rudin,*
Gerdt C.
Riise, and
Jan
Holmgren
Department of Medical Microbiology and
Immunology and Department of Respiratory Medicine, Göteborg
University, S-413 46 Göteborg, Sweden
Received 13 November 1998/Returned for modification 13 January
1999/Accepted 5 March 1999
Nasal vaccine delivery is superior to oral delivery in inducing
specific immunoglobulin A (IgA) and IgG antibody responses in the upper
respiratory tract. Although an antibody response in the nasal passages
is important in protecting against primary colonization with lung
pathogens, antibodies in the lungs are usually required as well. We
immunized 15 male volunteers twice nasally or orally with cholera toxin
B subunit (CTB) and determined the specific antibody levels in serum,
bronchoalveolar lavage (BAL) fluid, and urine before and 2 weeks after
immunization. Nasal immunization induced fivefold increases in the
levels of specific IgA antibodies in BAL fluid of most volunteers,
whereas there were no significant specific IgA responses after
oral immunization. The specific IgG antibody level increased
eightfold in BAL fluid in the nasally vaccinated subjects, and the
major part of IgG had most probably been transferred from serum. Since
the specific IgG response in serum was lower in the individuals
vaccinated orally, the IgG response in BAL fluid in this group was also
lower and not significant. In conclusion, nasal immunization is also preferable to the oral route when vaccinating against lower respiratory tract infections, and a systemic immune response is considerably more
important in the lower than in the upper respiratory tract. Moreover,
both nasal and oral immunizations were able to stimulate 6- to 10-fold
specific IgA and IgG responses in urine in about half of the
individuals, which indicates that distant mucosal vaccination might be
used to prevent adhesion of pathogens to the urogenital tract.
*
Corresponding author. Mailing address: Department of
Medical Microbiology and Immunology, Göteborg University,
Guldhedsgatan 10A, S-413 46 Göteborg, Sweden. Phone: 46 31 342 44 92. Fax: 46 31 82 01 60. E-mail:
anna.rudin{at}microbio.gu.se.
Infection and Immunity, June 1999, p. 2884-2890, Vol. 67, No. 6
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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