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논문 기본 정보

자료유형
학술저널
저자정보
Mirim Jin (Gachon University) Juhan Yoon (C&C Research Laboratories)
저널정보
대한면역학회 Immune Network Immune Network Vol.18 No.6
발행연도
2018.12
수록면
16 - 26 (11page)

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Atopic dermatitis (AD) is the most common pruritic inflammatory skin disease characterized by thickening of epidermis and dermis as well as by the infiltration of multiple pathogenic polarized T lymphocytes, including Th2, Th17, and Th22 cells. Significant progress has been made to develop targeted therapeutics for treating AD, e.g., Food and Drug Administrationapproved dupilumab, an antibody for dual targeting of IL-4 and IL-13 signaling pathways. Additionally, a growing body of published evidence and a promising result from the early stage of the clinical trial with ILV-094, an anti-IL-22 antibody, strongly support the notion that IL-22 is a potential therapeutic target for treating AD. Moreover, we also experimentally proved that IL-22 contributes to the pathophysiology of AD by employing a murine model of AD induced by epicutaneous sensitization. Here, we review recent preclinical and clinical findings that have advanced our understanding of the roles of IL-22 and Th22 cells in skin inflammation. We conclude that blockade of IL-22 signaling may be a promising therapeutic approach for the treatment of AD.

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ABSTRACT
INTRODUCTION
THE SKIN AS A MAJOR ROUTE OF ALLERGEN SENSITIZATION FOR ALLERGIC DISEASES
MOUSE MODEL OF AD TRIGGERED BY EPICUTANEOUSSENSITIZATION
POTENTIAL ROLE OF IL-22 AND TH22 CELLS IN AD
PLAUSIBLE MECHANISMS OF TH22 CELL POLARIZATIONIN THE SKIN
POTENTIAL THERAPEUTIC TARGETING OF IL-22/TH22SIGNALING PATHWAYS IN AD
ALTERNATIVE THERAPEUTIC APPROACHES FOR THETREATMENT OF AD
FUTURE PERSPECTIVES
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2019-517-000338091