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Natural killer T cells are not the predominant T cell in asthma and likely modulate, not cause, asthma
- Source :
- Journal of Allergy and Clinical Immunology. 125:980-984
- Publication Year :
- 2010
- Publisher :
- Elsevier BV, 2010.
-
Abstract
- Asthma is a multifactorial disease of the airways characterized by airway inflammation, mucus hypersecretion, and airway hyperresponsiveness. Conventional MHC class II–restricted CD4 + T cells are considered a key cell in asthma pathogenesis because they have a broad T-cell receptor repertoire, providing specificity and reactivity to diverse protein allergens. This notion was challenged when a study found that invariant Natural Killer (NK) T cells were the predominant T cells in the lung and bronchoalveolar lavage fluid of all asthmatic subjects studied. This finding was provocative because invariant NKT cells have a very limited T-cell receptor repertoire and are specific for a restricted set of lipid antigens that bind to CD1d, a nonpolymorphic MHC-like molecule. However, multiple subsequent studies failed to replicate the initial study and instead found that invariant NKT cells are present as a small fraction of the total T cells in the asthmatic lung. Thus, we believe that although CD1d-restricted NKT cells might play a role in modulating the asthmatic phenotype, they are not the critical drivers of the asthmatic response, a role we believe is still held by conventional MHC class II–restricted CD4 + T cells.
- Subjects :
- medicine.diagnostic_test
biology
T cell
Immunology
CD1
chemical and pharmacologic phenomena
Dendritic cell
respiratory system
Natural killer T cell
respiratory tract diseases
Interleukin 21
Bronchoalveolar lavage
medicine.anatomical_structure
CD1D
MHC class I
medicine
biology.protein
Immunology and Allergy
Subjects
Details
- ISSN :
- 00916749
- Volume :
- 125
- Database :
- OpenAIRE
- Journal :
- Journal of Allergy and Clinical Immunology
- Accession number :
- edsair.doi...........288784d42d5cce0d3cc30b2240b4e990
- Full Text :
- https://doi.org/10.1016/j.jaci.2010.01.032