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Frequency and role of NKp46 and NKG2A in hepatitis B virus infection

BACKGROUND AND AIM: Natural Killer (NK) cells are involved in the control of viral infection. However, the role of NK cells in chronic hepatitis B (CHB) remains unclear. This study investigated the frequencies and roles of NK cells in CHB, with a focus on activating receptor NKp46 and inhibitory rec...

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Detalles Bibliográficos
Autores principales: Yoshioka, Teppei, Tatsumi, Tomohide, Miyagi, Takuya, Mukai, Kaori, Nishio, Kumiko, Nishio, Akira, Yokoyama, Yoshinobu, Suda, Takahiro, Kegasawa, Tadashi, Shigekawa, Minoru, Hikita, Hayato, Sakamori, Ryotaro, Takehara, Tetsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362099/
https://www.ncbi.nlm.nih.gov/pubmed/28328926
http://dx.doi.org/10.1371/journal.pone.0174103
Descripción
Sumario:BACKGROUND AND AIM: Natural Killer (NK) cells are involved in the control of viral infection. However, the role of NK cells in chronic hepatitis B (CHB) remains unclear. This study investigated the frequencies and roles of NK cells in CHB, with a focus on activating receptor NKp46 and inhibitory receptor NKG2A. PATIENTS/METHOD: Peripheral blood lymphocytes were obtained from 71 CHB patients and 37 healthy subjects (HS). The expressions of NKp46 and NKG2A were analyzed using flow cytometry. The role of NKp46-ligand was assessed using an in vitro co-culture system. Cytotoxicity and IFN-γ production in NK cells were evaluated using RT-PCR and flow cytometry. RESULTS: CHB patients were classified into treatment-naïve patients with low HBV DNA titer (CHB-L; n = 28), high HBV DNA titer (CHB-H; n = 24) by the cut-off level of serum HBV DNA 4 log copies/ml, and patients receiving nucleos(t)ide analogue (CHB-NA; n = 19). The expressions of NKp46 and NKG2A were higher in CHB-H than in HS/CHB-L/CHB-NA. HepG2.2.15 had higher NKp46-ligand expression than HepG2. When NK cells from HS were co-cultured with HepG2.2.15, inhibition of the NKp46 and NKp46-ligand interaction by anti-NKp46 antibody significantly reduced cytolysis of HepG2.2.15 and IFN-γ production. However, those reductions were not observed in co-culture with HepG2. Additionally, NK cells that highly expressed NKp46 also highly expressed NKG2A (NKp46(high)NKG2A(high) subset). The frequencies of NKp46(high)NKG2A(high) subset in CHB-H were higher than those in HS/CHB-L/CHB-NA. Among treatment-naïve CHB patients, the frequencies of NKp46(high)NKG2A(high) subset were positively correlated with serum ALT (P<0.01, r = 0.45) and HBV DNA (P<0.01, r = 0.59) levels. The expressions of Fas-L, STAT1, TRAIL and CD107a were higher and IFN-γ expression was lower in the NKp46(high)NKG2A(high) subset than in the other subsets. CONCLUSION: The NKp46 and NKp46-ligand interaction contributes to NK cell activation. A novel NK cell subset, the NKp46(high)NKG2A(high) subset, may be associated with liver injury and HBV replication.