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Age-dependent natural killer cell and interferon γ deficits contribute to severe pertussis in infant mice.
- Source :
- Journal of Leukocyte Biology; Jun2024, Vol. 115 Issue 6, p1143-1153, 11p
- Publication Year :
- 2024
-
Abstract
- Many respiratory infections are selectively injurious to infants, yet the etiology of age-associated susceptibility is unknown. One such bacterial pathogen is Bordetella pertussis. In adult mice, innate interferon γ (IFN-γ) is produced by natural killer (NK) cells and restricts infection to the respiratory tract. In contrast, infant pertussis resembles disease in NK cell– and IFN-γ–deficient adult mice that experience disseminated lethal infection. We hypothesized that infants exhibit age-associated deficits in NK cell frequency, maturation, and responsiveness to B. pertussis , associated with low IFN-γ levels. To delineate mechanisms behind age-dependent susceptibility, we compared infant and adult mouse models of infection. Infection in infant mice resulted in impaired upregulation of IFN-γ and substantial bacterial dissemination. B. pertussis –infected infant mice displayed fewer pulmonary NK cells than adult mice. Furthermore, the NK cells in the infant mouse lungs had an immature phenotype, and the infant lung showed no upregulation of the IFN-γ–inducing cytokine IL-12p70. Adoptive transfer of adult NK cells into infants, or treatment with exogenous IFN-γ, significantly reduced bacterial dissemination. These data indicate that the lack of NK cell–produced IFN-γ significantly contributes to infant fulminant pertussis and could be the basis for other pathogen-induced, age-dependent respiratory diseases. [ABSTRACT FROM AUTHOR]
- Subjects :
- KILLER cells
WHOOPING cough
INFANTS
BORDETELLA pertussis
RESPIRATORY infections
Subjects
Details
- Language :
- English
- ISSN :
- 07415400
- Volume :
- 115
- Issue :
- 6
- Database :
- Complementary Index
- Journal :
- Journal of Leukocyte Biology
- Publication Type :
- Academic Journal
- Accession number :
- 177680918
- Full Text :
- https://doi.org/10.1093/jleuko/qiae020