Anaphylaxis |
Human CD33 (Siglec-3) |
hCD33 knock-in |
Suppresses mast cell activation and protects against anaphylaxis (Duan et al., 2019) |
|
Siglec-6 |
Humanized |
Protects against anaphylaxis and reduces mast cell-derived mediators (Schanin et al., 2022) |
|
Siglec-8 |
Siglec-8 knock-in and humanized |
Suppresses mast cell activation and protects against anaphylaxis (Duan et al., 2021; Youngblood et al., 2019b) |
Allergic asthma |
Siglec-F |
Wild type vs. Siglecf−/−, St3gal3−/−, Muc5bΔ/Δ
|
Lack of Siglec-F or its ligands exacerbate blood, bone marrow, and airway eosinophilia (Kiwamoto et al., 2014; Kiwamoto et al., 2015; Suzukawa et al., 2013; Zhang et al., 2007) |
Allergen-induced eosinophilic inflammation |
Siglec-F |
Wild type |
Anti-Siglec-F Ab administration decreases blood and tissue eosinophil numbers and ameliorates disease severity (Camilleri et al., 2021; Rubinstein et al., 2011; Song et al., 2009a; Song et al., 2009b) |
EGIDs |
Siglec-8 |
Siglec-8 transgenic |
Reduces blood and tissue eosinophil numbers, diminishes type-2 inflammatory cytokines and chemokines, reduces mast cell GI infiltration (Youngblood et al., 2019a) |
IL-33-mediated inflammation |
Siglec-8 |
Siglec-8 transgenic |
Reduces neutrophil and eosinophil infiltration, decreases inflammatory mediators (Schanin et al., 2020) |
TLR-mediated inflammation, viral infection |
Siglec-8 |
Siglec-8 transgenic |
Reduces airway inflammation and protects against virus-induced pathology (Gebremeskel et al., 2021) |