TY - JOUR
T1 - Skin-infiltrating basophils promote atopic dermatitis-like inflammation via IL-4 production in mice
AU - Yamanishi, Yoshinori
AU - Mogi, Kotone
AU - Takahashi, Kazufusa
AU - Miyake, Kensuke
AU - Yoshikawa, Soichiro
AU - Karasuyama, Hajime
N1 - Funding Information:
We thank Dr William E. Paul for providing IL-4 reporter G4 (Il4GFP/+) mice; R. Sasaki, T. Nagao, and T. Kojima for technical support; all the members of the Karasuyama laboratory for helpful discussions; and M. Kinoshita for secretary assistance. This work was supported by research grants from the Japanese Ministry of Education, Culture, Sports, Science and Technology (19K07501 to YY and 19H01025 to HK); Kobayashi Foundation (to YY); and Hoyu Science Foundation (to YY).
Funding Information:
We thank Dr William E. Paul for providing IL‐4 reporter G4 (Il4GFP/+) mice; R. Sasaki, T. Nagao, and T. Kojima for technical support; all the members of the Karasuyama laboratory for helpful discussions; and M. Kinoshita for secretary assistance. This work was supported by research grants from the Japanese Ministry of Education, Culture, Sports, Science and Technology (19K07501 to YY and 19H01025 to HK); Kobayashi Foundation (to YY); and Hoyu Science Foundation (to YY).
Publisher Copyright:
© 2020 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Background: Patients with atopic dermatitis (AD) often show the infiltration of basophils in the affected skin. Because basophils represent only a minor fraction among cellular infiltrates in the skin lesion, the functional significance of skin-infiltrating basophils in AD pathogenesis remains ill-defined. In this study, we aimed to clarify the role of basophils and their effector molecules triggering skin inflammation in oxazolone (OX)-induced murine model of AD. Methods: A panel of mouse strains were sensitized and repeatedly challenged with topical applications of OX to induce AD-like skin inflammation. Both local and systemic Th2 immune responses were analyzed. Results: Basophils progressively accumulated in the skin lesion but barely in draining lymph nodes (LNs). When basophils were depleted during the elicitation phase, skin inflammation was ameliorated while Th2 cell differentiation in draining LNs remained intact. The expression of IL-4 was highly upregulated in the affected skin, and basophils turned out to be the major producers of IL-4 among cellular infiltrates, suggesting the involvement of basophil-derived IL-4 in the Th2 skin inflammation. Indeed, basophil-specific IL-4-deficient mice displayed attenuated skin inflammation with a marked reduction of IL-4 in the skin lesion, even though cutaneous basophil infiltration and serum levels of IgE remained intact. Conclusions: Skin-infiltrating basophils promoted OX-induced AD-like skin inflammation through their local production of IL-4, rather than the induction of Th2 cell differentiation in draining LNs. This study suggests that the selective targeting of basophils could be a beneficial strategy in the treatment of a certain type of AD.
AB - Background: Patients with atopic dermatitis (AD) often show the infiltration of basophils in the affected skin. Because basophils represent only a minor fraction among cellular infiltrates in the skin lesion, the functional significance of skin-infiltrating basophils in AD pathogenesis remains ill-defined. In this study, we aimed to clarify the role of basophils and their effector molecules triggering skin inflammation in oxazolone (OX)-induced murine model of AD. Methods: A panel of mouse strains were sensitized and repeatedly challenged with topical applications of OX to induce AD-like skin inflammation. Both local and systemic Th2 immune responses were analyzed. Results: Basophils progressively accumulated in the skin lesion but barely in draining lymph nodes (LNs). When basophils were depleted during the elicitation phase, skin inflammation was ameliorated while Th2 cell differentiation in draining LNs remained intact. The expression of IL-4 was highly upregulated in the affected skin, and basophils turned out to be the major producers of IL-4 among cellular infiltrates, suggesting the involvement of basophil-derived IL-4 in the Th2 skin inflammation. Indeed, basophil-specific IL-4-deficient mice displayed attenuated skin inflammation with a marked reduction of IL-4 in the skin lesion, even though cutaneous basophil infiltration and serum levels of IgE remained intact. Conclusions: Skin-infiltrating basophils promoted OX-induced AD-like skin inflammation through their local production of IL-4, rather than the induction of Th2 cell differentiation in draining LNs. This study suggests that the selective targeting of basophils could be a beneficial strategy in the treatment of a certain type of AD.
KW - animal models
KW - atopic dermatitis
KW - basophil
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U2 - 10.1111/all.14362
DO - 10.1111/all.14362
M3 - Article
C2 - 32406065
AN - SCOPUS:85085612203
SN - 0105-4538
VL - 75
SP - 2613
EP - 2622
JO - Allergy: European Journal of Allergy and Clinical Immunology
JF - Allergy: European Journal of Allergy and Clinical Immunology
IS - 10
ER -