TY - JOUR
T1 - Polyclonal IgE induces mast cell survival and cytokine production
AU - Kashiwakura, Jun Ichi
AU - Kawakami, Yuko
AU - Yuki, Keisuke
AU - Zajonc, Dirk M.
AU - Hasegawa, Shunji
AU - Tomimori, Yoshiaki
AU - Caplan, Benjamin
AU - Saito, Hirohisa
AU - Furue, Masutaka
AU - Oettgen, Hans C.
AU - Okayama, Yoshimichi
AU - Kawakami, Toshiaki
N1 - Funding Information:
This study was supported by grants from the National Institutes of Health AI50209 (T.K.) and AI054471 (H. C.O.) and Grants-in-Aid for Scientific Research (C) program of the Ministry of Education, Culture, Sports, Science and Technology of the Japanese Government (project No. 20591195 to Y.O.).
PY - 2009
Y1 - 2009
N2 - Background: Ag-dependent activation of IgE-bearing mast cells is a critical first step in immediate hypersensitivity and other allergic responses. Recent studies have revealed Ag-independent effects of monoclonal mouse IgE molecules on mast cell survival and activation. However, no studies have been performed on the effects of polyclonal IgE molecules. Here, we tested whether polyclonal mouse and human IgE molecules affect survival and cytokine production in mast cells. Methods: Mast cells were cultured in the presence of polyclonal mouse and human IgE molecules, and cell survival and cytokine production were analyzed. Results: Polyclonal mouse IgE molecules in sera from mice with atopic dermatitis-like allergic skin inflammation, enhanced survival and cytokine production in mast cell cultures. Similar to the effects of monoclonal IgE, the polyclonal IgE effects were mediated by the high-affinity IgE receptor, FcεRI. Human polyclonal IgE molecules present in sera from atopic dermatitis patients were also capable of activating mast cells, and inducing IL-8 production in human cord blood-derived mast cells. Conclusions: These results imply that polyclonal IgE in atopic dermatitis and other atopic conditions might modulate mast cell number and function, thus amplifying the allergic response.
AB - Background: Ag-dependent activation of IgE-bearing mast cells is a critical first step in immediate hypersensitivity and other allergic responses. Recent studies have revealed Ag-independent effects of monoclonal mouse IgE molecules on mast cell survival and activation. However, no studies have been performed on the effects of polyclonal IgE molecules. Here, we tested whether polyclonal mouse and human IgE molecules affect survival and cytokine production in mast cells. Methods: Mast cells were cultured in the presence of polyclonal mouse and human IgE molecules, and cell survival and cytokine production were analyzed. Results: Polyclonal mouse IgE molecules in sera from mice with atopic dermatitis-like allergic skin inflammation, enhanced survival and cytokine production in mast cell cultures. Similar to the effects of monoclonal IgE, the polyclonal IgE effects were mediated by the high-affinity IgE receptor, FcεRI. Human polyclonal IgE molecules present in sera from atopic dermatitis patients were also capable of activating mast cells, and inducing IL-8 production in human cord blood-derived mast cells. Conclusions: These results imply that polyclonal IgE in atopic dermatitis and other atopic conditions might modulate mast cell number and function, thus amplifying the allergic response.
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U2 - 10.2332/allergolint.08-OA-0080
DO - 10.2332/allergolint.08-OA-0080
M3 - Article
C2 - 19542764
AN - SCOPUS:70449578104
SN - 1323-8930
VL - 58
SP - 411
EP - 419
JO - Allergology International
JF - Allergology International
IS - 3
ER -