Comparative characterization of B cells specific for HBV nucleocapsid and envelope proteins in patients with chronic hepatitis B

[Display omitted] •We developed a method for direct ex vivo visualization of HBV-specific B cells.•HBcAg- and HBsAg-specific B cells of patients with CHB differ in phenotype and function.•HBcAg-specific B cells are class-switched memory B cells and secrete antibodies.•HBV-specific B cells express cr...

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Veröffentlicht in:Journal of hepatology 2020-01, Vol.72 (1), p.34-44
Hauptverfasser: Le Bert, Nina, Salimzadeh, Loghman, Gill, Upkar Singh, Dutertre, Charles-Antoine, Facchetti, Floriana, Tan, Anthony, Hung, Magdeleine, Novikov, Nikolai, Lampertico, Pietro, Fletcher, Simon Paul, Kennedy, Patrick Thomas Francis, Bertoletti, Antonio
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Sprache:eng
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Zusammenfassung:[Display omitted] •We developed a method for direct ex vivo visualization of HBV-specific B cells.•HBcAg- and HBsAg-specific B cells of patients with CHB differ in phenotype and function.•HBcAg-specific B cells are class-switched memory B cells and secrete antibodies.•HBV-specific B cells express cross-presentation and innate immune genes.•HBV-specific B cell’s functional profiles shadow serological data of patients with CHB. Knowledge about the regulation of anti-HBV humoral immunity during natural HBV infection is limited. We recently utilized dual fluorochrome-conjugated HBsAg to demonstrate, in patients with chronic HBV (CHB) infection, the functional impairment of their HBsAg-specific B cells. However, the features of their HBcAg-specific B cells are unknown. Here we developed a method to directly visualize, select and characterize HBcAg-specific B cells in parallel with HBsAg-specific B cells. Fluorochrome-conjugated HBcAg reagents were synthesized and utilized to directly detect ex vivo HBcAg-specific B cells in 36 patients with CHB. The frequency, phenotype, functional maturation and transcriptomic profile of HBcAg-specific B cells was studied by flow cytometry, in vitro maturation assays and NanoString-based detection of expression of immune genes, which we compared with HBsAg-specific B cells and total B cells. HBcAg-specific B cells are present at a higher frequency than HBsAg-specific B cells in patients with CHB and, unlike HBsAg-specific B cells, they mature efficiently into antibody-secreting cells in vitro. Their phenotypic and transcriptomic profiles show that HBcAg-specific B cells are preferentially IgG+ memory B cells. However, despite their phenotypic and functional differences, HBcAg- and HBsAg-specific B cells from patients with CHB share an mRNA expression pattern that differs from global memory B cells and is characterized by high expression of genes indicative of cross-presentation and innate immune activity. During chronic HBV infection, a direct relation exists between serological detection of anti-HBs and anti-HBc antibodies, and the quantity and function of their respective specific B cells. However, the transcriptomic analysis performed in HBsAg- and HBcAg-specific B cells suggests additional roles of HBV-specific B cells beyond the production of antibodies. Protection of viral infection necessitates the production of antibodies that are generated by specialized cells of the immune system called B cells. During chronic HBV in
ISSN:0168-8278
1600-0641
DOI:10.1016/j.jhep.2019.07.015