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Updated: Jan 20, 2026

Isolation of Group 2 Innate Lymphoid Cells from Mouse Nasal Mucosa to Detect the Expression of CD226
Published on: May 10, 2022
Compartmentalized effects of aging on group 2 innate lymphoid cell development and function
Shanti S D'Souza1, Xiaofei Shen1, Ivan T H Fung1
1Department of Immunology and Microbial Disease, Albany Medical College, Albany, New York, USA.
Aging impairs lung group 2 innate lymphoid cells (ILC2), compromising immune responses. Restoring these cells in aged mice improved resistance to influenza infection, suggesting therapeutic potential.
Area of Science:
- Immunology
- Aging Research
- Innate Immunity
Background:
- Immunosenescence, the aging of the immune system, has complex effects on innate immunity.
- Group 2 innate lymphoid cells (ILC2) are crucial for lung homeostasis and repair, but their aging dynamics are unclear.
Purpose of the Study:
- To investigate the impact of aging on the development, function, and distribution of ILC2.
- To determine the role of aged ILC2 in pulmonary immune responses and susceptibility to infection.
Main Methods:
- Analysis of ILC2 development and function in young versus aged mice.
- Transcriptomic profiling of aged lung ILC2.
- Functional assays assessing cytokine production and response to influenza infection.
- Adoptive transfer experiments using young ILC2 into aged recipients.
Main Results:
- Aging promotes early ILC2 development in bone marrow but impairs their migration to the lungs.
- Aged lung ILC2 are functionally compromised, exhibiting reduced cytokine production and lower Cyp2e1 expression.
- Transfer of young ILC2 restored resistance to influenza infection in aged mice.
Conclusions:
- Aging causes compartmentalized defects in ILC2, affecting their development, localization, and function.
- Targeting tissue-resident ILC2 may offer therapeutic strategies to combat infections and diseases in the elderly.
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