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ADCC-MEDIATED CD56DIM NK CELL RESPONSES ARE ASSOCIATED WITH EARLY HBSAG CLEARANCE IN ACUTE HBV INFECTION
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The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA / Massachusetts Institute of Technology. Department of Biological Engineering. Cambridge, Massachussets, USA.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
University Hospital Basel. Dept. of Biomedicine. Basel, Switzerland.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
Massachusetts General Hospital, Boston, Massachusetts, USA.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Rio de Janeiro, RJ. Brasil.
Massachusetts General Hospital, Boston, Massachusetts, USA.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
University Hospital Basel. Dept. of Biomedicine. Basel, Switzerland.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
Massachusetts General Hospital, Boston, Massachusetts, USA.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Rio de Janeiro, RJ. Brasil.
Massachusetts General Hospital, Boston, Massachusetts, USA.
The Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts. USA.
Abstract
Hepatitis B virus (HBV) affects up to 400 million people worldwide and accounts for approximately one million deaths per year from liver pathologies. Current treatment regimens are effective in suppressing viremia but usually have to be taken indefinitely, warranting research into new therapeutic approaches. Acute HBV infection in adults almost universally results in resolution of viremia, with the exception of immunocompromised persons, suggesting that the immune response can functionally cure or even eradicate HBV infection.
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