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Infection and Immunity, February 2000, p. 672-679, Vol. 68, No. 2
Department of Molecular Biology and
Immunology, University of North Texas Health Science Center in Fort
Worth, Fort Worth, Texas 761071;
Department of Microbiology and Immunobiology Vaccine Center,
University of Alabama at Birmingham, Birmingham, Alabama
352942; and Department of Mucosal
Immunology, Research Institute for Microbial Diseases, Osaka
University, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan3
Received 2 July 1999/Returned for modification 21 September
1999/Accepted 17 November 1999
The purpose of the present study was to determine the immunologic
responses, particularly immunopathologic reactions, associated with
nasal immunization with the mucosal adjuvant, cholera toxin (CT).
BALB/c mice were nasally immunized with tetanus toxoid (TT) combined
with CT, and the responses of these mice were determined. After nasal
immunization, mice produce a serum antibody response, primarily of the
immunoglobulin G (IgG) isotype of predominantly IgG1 subclass, against
both TT and CT. Along with the antibody responses, we also found that
inflammatory reactions, which could be potentially fatal, developed
within the lung. Furthermore, IgE responses were also induced after
nasal immunization, and these responses were associated with the
detection of interleukin 5 in the serum. Thus, nasal immunization with
TT plus CT likely results in the activation of Th2 cells, which may
contribute to serious immunopathologic reactions in the lung.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Mucosally Induced Immunoglobulin E-Associated
Inflammation in the Respiratory Tract
*
Corresponding author. Mailing address: Department of
Molecular Biology and Immunology, University of North Texas Health
Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107. Phone:
(817) 735-2116. Fax: (817) 735-2118. E-mail:
jsimecka{at}hsc.unt.edu.
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