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Published on: March 30, 2018
The CD56-CD16+ NK cell subset in chronic infections
Alexander T H Cocker1,2, Lisbeth A Guethlein1,2, Peter Parham1,2
1Department of Structural Biology, Stanford University School of Medicine, Stanford, CA, U.S.A.
Chronic viral infections alter the immune system, leading to the differentiation of natural killer (NK) cells. This review focuses on the CD56-CD16+ NK cell subset, its association with HIV-1, and its role in chronic infections.
Area of Science:
- Immunology
- Virology
Background:
- Long-term viral infections can induce significant changes in the human immune system.
- Natural killer (NK) cells, crucial for innate immunity, differentiate into distinct subsets in response to chronic infections.
- The CD56-CD16+ NK cell subset is found in high frequencies during Human Immunodeficiency Virus type 1 (HIV-1) infection.
Approach:
- This review examines the evidence linking CD56-CD16+ NK cells to chronic viral infections.
- It explores potential immunological pathways altered by long-term infections that drive NK cell subset differentiation.
- The role of human leukocyte antigen (HLA) class-I molecules in regulating NK cell function and frequencies is highlighted.
Key Points:
- Increasing evidence supports the classification of CD56-CD16+ cells as a distinct NK cell subset.
- Variations in HLA expression, influenced by both viral factors and host genetics, correlate with CD56-CD16+ NK cell frequencies.
- The CD56-CD16+ NK cell subset may exhibit functional similarities to CD56+CD16+ NK cells in antibody-dependent cell cytotoxicity.
Conclusions:
- The CD56-CD16+ NK cell subset represents a significant adaptation to chronic viral infections like HIV-1.
- Understanding the differentiation and function of this subset is crucial for comprehending immune responses to persistent viral challenges.
- Further research into CD56-CD16+ NK cell subpopulations may reveal nuanced degranulation capacities and therapeutic targets.
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