2019
DOI: 10.1007/978-981-13-9151-4_6
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Present and Future Therapies for Chronic Hepatitis B

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Cited by 36 publications
(29 citation statements)
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“…CHB patients undergoing chronic inflammation, angiogenesis, HBV integration and metabolism, and oxidative damage develop HCC ultimately 26 . It is widely accepted that NAs can effectively prevent the progression or delay the development of HCC in CHB patients 27,28 . Therefore, ETV, TDF, and other NAs are recommended by current guidelines, especially ETV and TDF that are regarded as the first‐line therapy, 29,30 but no common consensus exists on which drug should be selected as the first choice for CHB patients to reduce the risk of HCC.…”
Section: Discussionmentioning
confidence: 99%
“…CHB patients undergoing chronic inflammation, angiogenesis, HBV integration and metabolism, and oxidative damage develop HCC ultimately 26 . It is widely accepted that NAs can effectively prevent the progression or delay the development of HCC in CHB patients 27,28 . Therefore, ETV, TDF, and other NAs are recommended by current guidelines, especially ETV and TDF that are regarded as the first‐line therapy, 29,30 but no common consensus exists on which drug should be selected as the first choice for CHB patients to reduce the risk of HCC.…”
Section: Discussionmentioning
confidence: 99%
“…Preliminary in vitro data suggest potential in the application of both rhIFNα and Zelnate in the treatment of clinical EEHV infections and give a plausible mode of action to justify their use 40 41. Although EEHVs are likely to possess IFN‐evasion strategies as described in other herpesviruses,42–44 the concept of head‐start immunity has been proposed,45 whereby these viral defences can be pre‐empted and, with sufficient and timely activation of the IFN system, can overcome infection, as highlighted by IFN‐based treatment strategies for chronic hepatitis B virus 46. EEHV‐HD is thought to be the result of primary infection in immunologically naive animals, following the decline of maternally derived antibodies 47.…”
Section: Discussionmentioning
confidence: 99%
“… 1 The exact mechanism of how PEG-IFN promotes HBsAg clearance remains unknown, and studies on predictors of HBsAg loss are still in the exploratory stage. 9 11 However, there is accumulating evidence that PEG-IFN predominantly expands the NK cells compartment without boosting virus-specific T cells in HBV. 12 , 13 NK cells respond quickly to stimulants.…”
Section: Discussionmentioning
confidence: 99%