scholarly journals Innate IL-17A Enhances IL-33-Independent Skin Eosinophilia and IgE Response on Subcutaneous Papain Sensitization

2021 ◽  
Vol 141 (1) ◽  
pp. 105-113.e14 ◽  
Author(s):  
Seiji Kamijo ◽  
Mutsuko Hara ◽  
Mayu Suzuki ◽  
Susumu Nakae ◽  
Hideoki Ogawa ◽  
...  
Keyword(s):  
1996 ◽  
Vol 26 (4) ◽  
pp. 452-460 ◽  
Author(s):  
J. SAVOLAINEN ◽  
A. RANTALA ◽  
M. NERMES ◽  
L. LEHTONEN ◽  
M. VIANDER

2007 ◽  
Vol 142 (2) ◽  
pp. 257-263 ◽  
Author(s):  
A. Inoue ◽  
T. Yasuda ◽  
T. Yamamoto ◽  
Y. Yamanashi

2012 ◽  
Vol 209 (2) ◽  
pp. 353-364 ◽  
Author(s):  
Huizhong Xiong ◽  
Jayashree Dolpady ◽  
Matthias Wabl ◽  
Maria A. Curotto de Lafaille ◽  
Juan J. Lafaille

IgE antibodies with high affinity for their antigens can be stably cross-linked at low concentrations by trace amounts of antigen, whereas IgE antibodies with low affinity bind their antigens weakly. In this study, we find that there are two distinct pathways to generate high and low affinity IgE. High affinity IgE is generated through sequential class switching (μ→γ→ε) in which an intermediary IgG phase is necessary for the affinity maturation of the IgE response, where the IgE inherits somatic hypermutations and high affinity from the IgG1 phase. In contrast, low affinity IgE is generated through direct class switching (μ→ε) and is much less mutated. Mice deficient in IgG1 production cannot produce high affinity IgE, even after repeated immunizations. We demonstrate that a small amount of high affinity IgE can cause anaphylaxis and is pathogenic. Low affinity IgE competes with high affinity IgE for binding to Fcε receptors and prevents anaphylaxis and is thus beneficial.


2021 ◽  
Author(s):  
M Weckmann ◽  
T Bahmer ◽  
J M Bülow Sand ◽  
S Rank Rønnow ◽  
D J Leeming ◽  
...  
Keyword(s):  

1999 ◽  
Vol 166 (2) ◽  
pp. 77-80 ◽  
Author(s):  
Izumi Horiuchi ◽  
Yuji Kawano ◽  
Kenji Yamasaki ◽  
Hidenori Matsuo ◽  
Motozumi Minohara ◽  
...  

F1000Research ◽  
2019 ◽  
Vol 8 ◽  
pp. 736 ◽  
Author(s):  
Andrea J. Luker ◽  
Joseph C. Lownik ◽  
Daniel H. Conrad ◽  
Rebecca K. Martin

Immunoglobulin E (IgE), though constitutively present at low levels, is most commonly studied in atopic disease where it plays a vital role in mast cell degranulation and in initiating a T helper 2 (Th2) response. With the advent of better detection assays, however, researchers are discovering the importance of IgE in actively contributing to many disease states and pathologies. This review will discuss the latest findings in IgE beyond its role in allergies and recently discovered roles for IgE in its cell-bound form on FcεRI-expressing effector cells like monocytes and dendritic cells. In terms of parasites, we will discuss helminth-induced IgE that appears to protect the worms from immune recognition and a tick-borne illness that elicits an IgE response against red meat. Next, we describe recent findings of how auto-reactive IgE can contribute to the progression of lupus and induce organ damage. Finally, we summarize the emerging roles of IgE in tumor surveillance and antibody-dependent cytotoxicity. We additionally discuss recent or ongoing clinical trials that either target harmful IgE or use the unique characteristics of the isotype.


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