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      Primary adrenal insufficiency is associated with impaired natural killer cell function: a potential link to increased mortality

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          Abstract

          Objective

          Mortality in patients with primary adrenal insufficiency (PAI) is significantly increased, with respiratory infections as a major cause of death. Moreover, patients with PAI report an increased rate of non-fatal infections. Neutrophils and natural killer (NK) cells are innate immune cells that provide frontline protection against invading pathogens. Thus, we compared the function and phenotype of NK cells and neutrophils isolated from PAI patients and healthy controls to ascertain whether altered innate immune responses could be a contributory factor for the increased susceptibility of PAI patients to infection.

          Design and methods

          We undertook a cross-sectional study of 42 patients with PAI due to autoimmune adrenalitis ( n = 37) or bilateral adrenalectomy ( n = 5) and 58 sex- and age-matched controls. A comprehensive screen of innate immune function, consisting of measurements of neutrophil phagocytosis, reactive oxygen species production, NK cell cytotoxicity (NKCC) and NK cell surface receptor expression, was performed on all subjects.

          Results

          Neutrophil function did not differ between PAI and controls. However, NKCC was significantly reduced in PAI (12.0 ± 1.5% vs 21.1 ± 2.6%, P < 0.0001). Phenotypically, the percentage of NK cells expressing the activating receptors NKG2D and NKp46 was significantly lower in PAI, as was the surface density of NKG2D (all P < 0.0001). Intracellular granzyme B expression was significantly increased in NK cells from PAI patients ( P < 0.01).

          Conclusions

          Adrenal insufficiency is associated with significantly decreased NKCC, thereby potentially compromising early recognition and elimination of virally infected cells. This potential impairment in anti-viral immune defense may contribute to the increased rate of respiratory infections and ultimately mortality in PAI.

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          Most cited references32

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          NK cell recognition.

          The integrated processing of signals transduced by activating and inhibitory cell surface receptors regulates NK cell effector functions. Here, I review the structure, function, and ligand specificity of the receptors responsible for NK cell recognition.
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            Recognition of haemagglutinins on virus-infected cells by NKp46 activates lysis by human NK cells.

            Natural killer (NK) cells destroy virus-infected and tumour cells, apparently without the need for previous antigen stimulation. In part, target cells are recognized by their diminished expression of major histocompatibility complex (MHC) class I molecules, which normally interact with inhibitory receptors on the NK cell surface. NK cells also express triggering receptors that are specific for non-MHC ligands; but the nature of the ligands recognized on target cells is undefined. NKp46 is thought to be the main activating receptor for human NK cells. Here we show that a soluble NKp46-immunoglobulin fusion protein binds to both the haemagglutinin of influenza virus and the haemagglutinin-neuraminidase of parainfluenza virus. In a substantial subset of NK cells, recognition by NKp46 is required to lyse cells expressing the corresponding viral glycoproteins. The binding requires the sialylation of NKp46 oligosaccharides, which is consistent with the known sialic binding capacity of the viral glycoproteins. These findings indicate how NKp46-expressing NK cells may recognize target cells infected by influenza or parainfluenza without the decreased expression of target-cell MHC class I protein.
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              Diagnosis and management of adrenal insufficiency.

              Adrenal insufficiency continues to be a challenge for patients, their physicians, and researchers. During the past decade, long-term studies have shown increased mortality and morbidity and impaired quality of life in patients with adrenal insufficiency. These findings might, at least partially, be due to the failure of glucocorticoid replacement therapy to closely resemble physiological diurnal secretion of cortisol. The potential effect of newly developed glucocorticoid drugs is a focus of research, as are the mechanisms potentially underlying increased morbidity and mortality. Adrenal crisis remains a threat to lives, and awareness and preventative measures now receive increasing attention. Awareness should be raised in medical teams and patients about adrenal insufficiency and management of adrenal crisis to improve clinical outcome.
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                Author and article information

                Journal
                Eur J Endocrinol
                Eur. J. Endocrinol
                EJE
                European Journal of Endocrinology
                Bioscientifica Ltd (Bristol )
                0804-4643
                1479-683X
                January 2017
                23 January 2017
                : 176
                : 4
                : 471-480
                Affiliations
                [1 ]Institute of Metabolism and Systems Research University of Birmingham, Birmingham, UK
                [2 ]Division of Endocrinology Diabetes, Metabolism, and Nutrition, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA
                [3 ]Institute of Inflammation and Ageing
                [4 ]Medical Research Council-Arthritis Research UK (MRC-ARUK) Centre for Musculoskeletal Ageing Research University of Birmingham, Birmingham, UK
                [5 ]Centre for Endocrinology Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
                Author notes
                Correspondence should be addressed to W Arlt; Email: w.arlt@ 123456bham.ac.uk
                [*]

                (I Bancos and J Hazeldine contributed equally to this work)

                Article
                EJE160969
                10.1530/EJE-16-0969
                5425935
                28223394
                dfd9e590-fba3-42a2-b44a-f4cb17446062
                © 2017 The authors

                This work is licensed under a Creative Commons Attribution 3.0 Unported License.

                History
                : 24 November 2016
                : 16 January 2017
                : 23 January 2017
                Categories
                Clinical Study

                Endocrinology & Diabetes
                Endocrinology & Diabetes

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