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. 2019 Jun 4;10:1263. doi: 10.3389/fimmu.2019.01263

Table 1.

Specificities of lung NK cells in non-neoplastic respiratory diseases.

Diseases Quantitative observations Qualitative considerations References
Systemic Auto-immune Diseases Sjögren Syndrome Normal absolute count of Activated (HLA-DR+) NK cells in BALF nd (30)
Systemic Sclerosis Normal absolute count of Activated (HLA-DR+) NK cells in BALF nd (30)
Anti-synthetase Syndrome NK cells infiltration of all areas of lung fibrosis NK cell expression of Granzyme B, Significant CD69 expression (31, 32)
Inflammatory Diseases and/or Fibrosing diseases Behçet Disease Lower proportion of NK cells in BALF Lower cytotoxicity (33)
Sarcoidosis Increased number of CD56bright NK cells in BALF Immature phenotype with NKG2Ahigh & KIRlow predominant phenotype. Higher capacity to produce IFN-γ and TNF-α cytokines (3436)
COPD Normal count of CD56+CD16+ lung NK cells Decreased CD8 expression associated with poor outcome, Higher cytotoxicity. Normal expression of the activating receptor NKG2D but abnormal expression of its ligands MICA/B by lung epithelial cells. (37)
Idiopathic Pulmonary Fibrosis Presence of NK cells in BALF Predisposing factor involving NKG2D-MICA/B pathway (38)
Allergy Asthma Hypersensitivity Pneumonitis Decreased proportion of CD56dim NK cells in BALF Higher number of NK cells in BALF Increased expression of Granzyme A nd (39) (29)
Infectious Diseases* Influenza A Virus** nd Resident NK cells are hyperfunctional after ex vivo Infection, including degranulation, granzyme B expression and IFN-gamma expression (11)
HCMV° Higher proportion of lung NKG2C+ NK cells (BALF) of patients with HCMV viremia following lung transplantation NKG2C+ NK cells are more mature and have higher proliferation capacities. All abnormalities are associated with poor outcomes. (28)

HLA, Human Leukocyte Antigen; BALF, Broncho-alveolar lavage fluid; nd, not determined; HCMV, Human Cyto-megalo-virus; COPD, chronic obstructive pulmonary disease;

*

focuses on human studies although animal models exists for various infections (including Mycobacterium Tuberculosis, Klebsiella Pneumoniae…).

**

first infectious disease in which analyses have been performed according to the definition of resident lung NK cells,

°

studies are available only in the context of lung transplantation.