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Contribution of mast cells to the T helper 2 response induced by simultaneous subcutaneous and oral immunization
Author(s) -
Aoki I.,
Itoh S.,
Yokota S.,
Tanaka S.I.,
Ishii N.,
Okuda K.,
Minami M.,
Klinman D. M.
Publication year - 1999
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.1999.00878.x
Subject(s) - mast (botany) , immunization , immunology , medicine , subcutaneous injection , mast cell , immune system
Summary This work examines the contribution of mast cells to the synergistic enhancement of the T helper 2 (Th2) immune response elicited following simultaneous oral and subcutaneous (s.c.) immunization. The s.c. route induced a Th1‐biased immune response, characterized by increased interferon‐γ (IFN‐γ) and immunoglobulin G2a (IgG2a) antibody production. In contrast, oral immunization stimulated a primarily Th2‐type response in which interleukin‐4 (IL‐4) and IgG1 antibody production were dominant. Simultaneous immunization also triggered a Th2‐biased response, the magnitude of which exceeded the additive effects of s.c. and oral immunization alone by greater than threefold. To analyse whether mast cells in gut‐associated lymphoid tissue contributed to this synergistic response, mast cell‐deficient mice WBB6F 1 ‐w/w v were studied. Whereas the primary response following simultaneously antigen administration was reduced only twofold in these animals compared with wild type controls WBB6F 1 ‐ +/+ (suggesting that mast cells were not needed to initiate Th2 immunity), reconstitution with bone‐marrow‐derived mast cells from WBB6F 1 ‐+/+ mice resulted in a superoptimal response (suggesting that mast cells contribute to the magnitude and perpetuation of these Th2‐biased responses).