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IL-22–producing “T22” T cells account for upregulated IL-22 in atopic dermatitis despite reduced IL-17–producing TH17 T cells
Open accessAbstract
Background Psoriasis and atopic dermatitis (AD) are common inflammatory skin diseases. An upregulated TH17/IL-23 pathway was demonstrated in psoriasis. Although potential involvement of TH17 T cells in AD was suggested during acute disease, the role of these cells in chronic AD remains unclear.Objective To examine differences in IL-23/TH17 signal between these diseases and establish relative frequencies of T-cell subsets in AD.Methods Skin biopsies and peripheral blood were collected from patients with chronic AD (n = 12) and psoriasis (n = 13). Relative frequencies of CD4+ and CD8+ T-cell subsets within these 2 compartments were examined by intracellular cytokine staining and flow cytometry.Results In peripheral blood, no significant difference was found in percentages of different T-cell subsets between these diseases. In contrast, psoriatic skin had significantly increased frequencies of TH1 and TH17 T cells compared with AD, whereas TH2 T cells were significantly elevated in AD. Distinct IL-22-producing CD4+ and CD8+ T-cell populations were significantly increased in AD skin compared with psoriasis. IL-22+CD8+ T-cell frequency correlated with AD disease severity.Conclusion Our data established that T cells could independently express IL-22 even with low expression levels of IL-17. This argues for a functional specialization of T cells such that "T17" and "T22" T-cells may drive different features of epidermal pathology in inflammatory skin diseases, including induction of antimicrobial peptides for "T17" T cells and epidermal hyperplasia for "T22" T-cells. Given the clinical correlation with disease severity, further characterization of "T22" T cells is warranted, and may have future therapeutic implications.
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“Circulating IL-22 correlates with the severity of AD and appears as a key driver in the inflammatory reaction116,119.”
From Atopic dermatitis: an expanding therapeutic pipeline for a complex disease (2022) · cites this paper as [116]
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“IL-22 is an important part of the transcriptomic signature in AD116,117.”
From Atopic dermatitis: an expanding therapeutic pipeline for a complex disease (2022) · cites this paper as [116]
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Clinical characteristics and management of dupilumab-associated ocular surface disease in Japan
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“Th22 cells in the skin lesions of patients with AD are more frequent than in those of patients with psoriasis [69].”
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Self-citationInterleukin antagonists for atopic dermatitis: a new era of therapy
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“Activation of IL-22 signaling has been associated with upregulation of antimicrobial peptides in the epidermis, promotion of keratinocyte proliferation and inhibition of their terminal differentiation, contributing significantly in skin barrier dysfunction and epidermal hyperplasia [47–50].”
BackgroundNagy, G., Doan‐Xuan, Q., Gáspár, K., Mócsai, G., Kapitány, A., Törőcsik, D., Bacsó, Z., Gyimesi, E., Remenyik, É., Bı́ró, T., et al. (2014) · Experimental Dermatology · doi:10.1111/exd.12342 · Cited by 5
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Adaptive Immunantworten und damit verbundene Triggerfaktoren bei atopischer Dermatitis
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A specific molecular signature for psoriasis and eczema.
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“However, other authors defend that activation of Th2 cells and of the Th22 pathway results in reactive epidermal hyperplasia (4).”
BackgroundAtopic Dermatitis and Allergic Contact Dermatitis
Leung, D. Y. M., & Boguniewicz, M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-37579-5.00011-8 · Cited by 4
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Phenotypes and endotypes of atopic dermatitis: Clinical implications
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Exploratory analyses of biomarkers in blood and stratum corneum in patients with atopic dermatitis
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“Received: 14 September 2022 / Accepted: 19 September 2022 http://dx.doi.org/10.1097/MD.0000000000031267 chemokine (TARC),[15,16] CCL22/macrophage-derived chemokine,[17,18] and the Th22-related cytokine IL-22[17,19] in the blood and skin.”
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“Moreover, the frequency of the IL-22-producing CD8+ T-cells is positively correlated with the severity of AD (10); IL-22, which is highly expressed in patients with AD, is deeply involved in epidermal hyperplasia and barrier defects (11,12).”
BackgroundYamaguchi, H., Ando, M., Iwashita, N., Takagi, Y., Kushiro, M., & Fukuyama, T. (2023) · Journal of Applied Toxicology · doi:10.1002/jat.4462 · Cited by 3
“As a result of dendritic proliferation and TNFα secretion, differentiation and activation of Th17 and ILC17 cells are promoted (Nograles et al., 2009).”
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Revisiting immunotherapeutic strategies for the management of atopic dermatitis
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Expression and Function of CCL17 in Atopic Dermatitis
Stutte, S., Gerbitzki, N., Novak, N., & Frster, I. (2012) · InTech eBooks · doi:10.5772/25704 · Cited by 4
“In psoriasis, Th17 cells act together with Th1 cells in disease pathogenesis (Lowes et al., 2008; Nograles et al., 2009).”
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Contribution of IL-22 to Experimental Skin Inflammation
Lecron, J., Paris, I., Bernard, F., & Morel, F. (2012) · Springer eBooks · doi:10.1007/978-3-0348-0522-3_22 · Cited by 3
“Not specific of psoriasis, Th22 is also increased in lesional skin of atopic dermatitis [54].”
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Editorial update on emerging treatments of atopic dermatitis
Ong, P. Y. (2012) · Expert Opinion on Emerging Drugs · doi:10.1517/14728214.2012.668884 · Cited by 3
“IL-22 expression is increased in AD lesions and contributes to the pathology of AD [9-11].”
BackgroundWu, Y., Wasikowski, R., Patrick, M. T., Gharaee‐Kermani, M., Xing, X., Billi, A. C., Kahlenberg, J. M., Julia, V., Gudjonsson, J. E., & Tsoi, L. C. (2025) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2025.08.026 · Cited by 3
Metadata
- Authors
- Nograles, K. E., Zaba, L. C., Shemer, A., Fuentes-Duculan, J., Cardinale, I., Kikuchi, T., Ramon, M., Bergman, R., Krueger, J. G., & Guttman-Yassky, E.
- Affiliations
- Rockefeller University (US)
- Technion – Israel Institute of Technology (IL)
- Venue
- Journal of Allergy and Clinical Immunology
- Publisher
- Elsevier BV
- Published
- 2009-06
- Volume
- 123
- Issue
- 6
- Pages
- 1244-1252.e2
- ISSN
- 0091-6749 (ISSN-L)
- PMC
- PMC2874584
- OpenAlex
- W2164098277
- Cited by
- 627
- References
- 30
- Citations by year
- 2026: 13 · 2025: 17 · 2024: 21 · 2023: 23 · 2022: 28 · 2021: 39 · 2020: 39 · 2019: 28 · 2018: 25 · 2017: 49 · 2016: 49 · 2015: 51 · 2014: 52 · 2013: 34 · 2012: 47
- FWCI
- 65.54
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Allergy and Clinical Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of General Medical Sciences (GM 07739, T32GM007739)
- National Center for Research Resources (UL1RR024143)
- Topics
- Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- atopic dermatitis, IL-22, IL-17, Th17 cells, Th2 cells, Th1 cells, IL-23, psoriasis, CD4+ T cells, CD8+ T cells, disease severity, epidermal hyperplasia, antimicrobial peptides, skin inflammation
- MeSH terms
- Interleukin-22, Adult, Chronic Disease, Dermatitis, Atopic, T-Lymphocytes, Helper-Inducer, Humans, Interleukins, Middle Aged, Psoriasis, T-Lymphocyte Subsets, Interleukin-17, Interleukin-23
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