Publication

γ/δ T cell-deficient mice have impaired mucosal immunoglobulin A responses

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Last modified
  • 02/25/2025
Type of Material
Authors
    Kohtaro Fujihashi, University of Alabama at BirminghamJerry R. McGhee, University of Alabama at BirminghamMi-Na Kweon, University of Alabama at BirminghamMax Cooper, Emory UniversitySusumu Tonegawa, Massachusetts Institute of TechnologyIchiro Takahashi, Osaka UniversityTakachika Hiroi, Osaka UniversityJiri Mestecky, University of Alabama at BirminghamHiroshi Kiyono, University of Alabama at Birmingham
Language
  • English
Date
  • 1996-04-01
Publisher
  • Rockefeller University Press
Publication Version
Copyright Statement
  • © Rockefeller University Press
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0022-1007
Volume
  • 183
Issue
  • 4
Start Page
  • 1929
End Page
  • 1935
Grant/Funding Information
  • This work was supported by U.S. Public Health Service grants AI-35932, DE-09837, AI-35544, AI-30366, DE-04217, DK-44240, AI-18958, AI-39816, and contract AI-15128 as well as grants from Ministry of Education, Science Sports and Cultures, Ministry of Health and Welfare, and Asahi Chemical Industry Co. Ltd. in Japan. M.D. Cooper and S. Tonegawa are Howard Hughes Medical Institute investigators.
Abstract
  • Mucosal tissues of mice are enriched in T cells that express the γ/δ T cell receptor. Since the function of these cells remains unclear, we have compared mucosal immune responses in γ/δ T cell receptor-deficient (TCRδ-/-) mice versus control mice of the same genetic background. The frequency of intestinal immunoglobulin (Ig) A plasma cells as well as IgA levels in serum, bile, saliva, and fecal samples were markedly reduced in TCRδ-/- mice. The TCRdelta-/- mice produced much lower levels of IgA antibodies when immunized orally with a vaccine of tetanus toxoid plus cholera toxin as adjuvant. Conversely, the antigen-specific IgM and IgG antibody responses were comparable to orally immunized control mice. Direct assessment of the cells forming antibodies against the tetanus toxoid and cholera toxin antigens indicated that significantly lower numbers of IgA antibody-producing cells were present in the intestinal lamina propria and Peyer's patches of TCRδ-/- mice compared with the orally immunized control mice. The selective reduction of IgA responses to ingested antigens in the absence of γ/δ T cells suggests a specialized role for γ/δ cells in mucosal immunity.
Author Notes
  • Address correspondence to Hiroshi Kiyono, Departments of Oral Biology and Microbiology, BBRB Room 761, Immunobiology Vaccine Center, University of Alabama at Birmingham, Medical Center, Birmingham, AL 35294-2170.
Keywords
Research Categories
  • Health Sciences, Immunology
  • Biology, Microbiology

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