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Mechanisms

Peripheral killer cells do not differentiate between asthma patients with or without fixed airway obstruction

, PhD, , PhD, , MBBS, FRCP, DM, , PhD, , PhD & , PhD
Pages 456-466 | Received 02 May 2016, Accepted 10 Sep 2016, Published online: 21 Dec 2016
 

ABSTRACT

Objective: The three main types of killer cells – CD8+ T cells, NK cells and NKT cells – have been linked to asthma and chronic obstructive pulmonary disease (COPD). However, their role in a small subset of asthma patients displaying fixed airway obstruction (FAO), similar to that seen in COPD, has not been explored. The objective of the present study was to investigate killer cell numbers, phenotype and function in peripheral blood from asthma patients with FAO, asthma patients without FAO, and healthy individuals. Methods: Peripheral CD8+ T cells (CD8+CD3+CD56), NK cells (CD56+CD3) and NKT-like cells (CD56+CD3+) of 14 asthma patients with FAO (post-bronchodilator FEV/FVC <0.7, despite clinician-optimised treatment), 7 asthma patients without FAO (post-bronchodilator FEV/FVC ≥ 0.7), and 9 healthy individuals were studied. Results: No significant differences were seen between the number, receptor expression, MAPK signalling molecule expression, cytotoxic mediator expression, and functional cytotoxicity of peripheral killer cells from asthma patients with FAO, asthma patients without FAO and healthy individuals. Conclusions: Peripheral killer cell numbers or functions do not differentiate between asthma patients with or without fixed airway obstruction.

Acknowledgments

We gratefully acknowledge our research nurse, Wendy Gerrard-Tarpey, for recruiting the participants.

Declaration of interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the article.

Funding

CT was funded by a University of Nottingham Molecular Medical Sciences PhD Student Scholarship and the Nottingham Respiratory Biomedical Research Unit. TH and LF were supported by the Nottingham Respiratory Biomedical Research Unit.

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