Table 1.
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 | (34–36) | |
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.