TY - JOUR PY - 2015// TI - Phenotype and functions of B cells in patients with acute brain injuries JO - Molecular immunology A1 - Chenouard, Alexis A1 - Chesneau, Mélanie A1 - Braza, Faouzi A1 - Dejoie, Thomas A1 - Cinotti, Raphael A1 - Roquilly, Antoine A1 - Brouard, Sophie A1 - Asehnoune, Karim SP - 350 EP - 356 VL - 68 IS - 2 Pt A N2 - BACKGROUND: Brain injuries (BI) induce a state of systemic immunosuppression, leading to a high risk of pneumonia. In this pilot study, we investigated the status of B cell compartment in BI patients.

METHODS: A prospective observational study was performed in 2 intensive care units in a university hospital. Blood samples were collected in 14 patients at day 1 and day 7 after acute BI. The phenotype and the ability of B cells to secrete IL-10 were compared to 11 healthy volunteers (HV).

RESULTS: Among the circulating lymphocytes, the frequency of B cells was significantly higher in BI patients compared to HV (p<0.001). B cells from BI patients displayed an activated profil on day 7 after BI, reflected by a significantly higher proportion of CD27(+) memory (p=0.01) and CD27(+) IgD(-) switched memory B cells (p=0.02), as well as a significantly higher blood level of IgA (p=0.001) and IgM (p<0.001) as compared to day 1. The frequency of IL-10 secreting B cells (IL-10(+) B cells) on day 1 and day 7 was significantly lower in BI patients compared to HV (p<0.05). Interestingly, we observed that all BI patients with high frequency of IL-10(+) B cells on day 1 displayed an episode of pneumonia, and had a longer duration of mechanical ventilation and ICU stay compared to BI patients with low proportion of IL-10(+) B cells.

CONCLUSION: This study provides an extensive description of the phenotype and function of B cells in BI patients. Our results suggest that IL-10(+) B cells could play a major role in immunosuppression after BI.

Language: en

LA - en SN - 0161-5890 UR - http://dx.doi.org/10.1016/j.molimm.2015.09.001 ID - ref1 ER -