The DOI matches its Crossref record; 66 of the 66 references it cites were found in a registry or an index.
Interleukin-33 and Interferon-γ Counter-Regulate Group 2 Innate Lymphoid Cell Activation during Immune Perturbation
Open accessAbstract
SUMMARY Group 2 innate lymphoid cells (ILC2) and regulatory T (Treg) cells are systemically induced by helminth infection but also sustain metabolic homeostasis in adipose tissue and contribute to tissue repair during injury. Here we show interleukin-33 (IL-33) mediates activation of ILC2 and Treg cells in resting adipose tissue, but also after helminth infection or treatment with IL-2. Unexpectedly, ILC2-intrinsic IL-33 activation was required for Treg cell accumulation in vivo, and was independent of ILC2 type 2 cytokines but partially dependent on direct co-stimulatory interactions via ICOSL-ICOS. IFN-γ inhibited ILC2 activation and Treg cell accumulation by IL-33 in infected tissue as well as adipose tissue, where repression increased with aging and high-fat diet-induced obesity. IL-33 and ILC2 are central mediators of type 2 immune responses that promote tissue and metabolic homeostasis, and IFN-γ suppresses this pathway, likely to promote inflammatory responses and divert metabolic resources necessary to protect the host.
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Cites
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Self-citationMacrophage-specific PPARγ controls alternative activation and improves insulin resistance
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“…associated with type 2 immunity, including ILC2s, eosinophils, and AAMs, with Treg cells in visceral adipose tissue (VAT) of resting mice (Cipolletta et al., 2012; Feuerer et al., 2009; Molofsky et al., 2013; Odegaard et al., 2007; Qiu et al., 2014; Vasanthakumar et al., 2015; Wu et al., 2011).”
BackgroundInnate production of TH2 cytokines by adipose tissue-associated c-Kit+Sca-1+ lymphoid cells
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Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity
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Eosinophils Sustain Adipose Alternatively Activated Macrophages Associated with Glucose Homeostasis
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Self-citationNormalization of obesity-associated insulin resistance through immunotherapy
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Cited by
Metabolic Inflammation and Insulin Resistance in Obesity
Wu, H., & Ballantyne, C. M. (2020) · Circulation Research · doi:10.1161/circresaha.119.315896 · Cited by 1,059
Interleukin-33 in tissue homeostasis, injury, and inflammation
Molofsky, A. B., Savage, A. K., & Locksley, R. M. (2015) · Immunity · doi:10.1016/j.immuni.2015.06.006 · Cited by 638
Self-citationType 2 immunity in the skin and lungs
Akdis, C. A., Arkwright, P. D., Brüggen, M.-C., Busse, W., Gadina, M., Guttman‐Yassky, E., Kabashima, K., Mitamura, Y., Vian, L., Wu, J., et al. (2020) · Allergy · doi:10.1111/all.14318 · Cited by 560
Panduro, M., Benoist, C., & Mathis, D. (2016) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095948 · Cited by 536
Immunotherapy: Reshape the Tumor Immune Microenvironment
LV, B., Wang, Y., Ma, D., Cheng, W., Liu, J., Yong, T., Chen, H., & Wang, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.844142 · Cited by 482
Metadata
- Authors
- Molofsky, A. B., Van Gool, F., Liang, H.-E., Van Dyken, S. J., Nussbaum, J. C., Lee, J., Bluestone, J. A., & Locksley, R. M.
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2015-07
- Volume
- 43
- Issue
- 1
- Pages
- 161-174
- ISSN
- 1074-7613 (ISSN-L)
- OpenAlex
- W1855313929
- Cited by
- 431
- References
- 66
- FWCI
- 19.79
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Molofsky, A. B., Van Gool, F., Liang, H.-E., Van Dyken, S. J., Nussbaum, J. C., Lee, J., Bluestone, J. A., & Locksley, R. M. (2015). Interleukin-33 and Interferon-γ Counter-Regulate Group 2 Innate Lymphoid Cell Activation during Immune Perturbation. Immunity. https://doi.org/10.1016/j.immuni.2015.05.019
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