Table 1.
Characteristics of anti hepatitis B virus drugs
|
Drug
|
Approve time (year)
|
Classification
|
Mechanism
|
Administration method
|
Metabolize
|
Major side effect
|
Drug resistance
|
| LAM | 1998 | NRTI | Competitive binding to HBV DNA polymerase binding site[64] | Oral administration | Kidney | Less side effects, may lead to myopathy or even rhabdomyolysis[65] | Susceptible to drug resistance, especially YMDD mutation[68] |
| LDT | 2008 | NRTI | Competitive binding to HBV DNA polymerase binding site[78] | Oral administration | Kidney | Myopathy and peripheral neuropathy[74] | The rate of drug resistance in long-term treatment was high, and the common drug resistance mutations were rtM204I and rtL180M [79,85] |
| ADV | 2002 | NtRTI | Competitive binding of HBV DNA polymerase binding site and embedding into viral DNA strand[71] | Oral administration | Kidney | Renal function damage[75] | Compared to LAM, the risk of resistance is low[71] |
| ETV | 2005 | NRTI | Competitive binding to HBV DNA polymerase binding site[12,13] | Oral administration | Kidney | Less side effects, possible renal function damage[14] | Low resistance rate, but resistance to LAM-resistant HBV increased[16,20] |
| TDF | 2008 | NtRTI | Competitive binding of HBV DNA polymerase binding site and embedding into viral DNA strand[26] | Oral administration | Kidney | Bone and kidney injury[34] | Low risk of drug resistance |
| TAF | 2016 | NtRTI | Competitive binding to HBV DNA polymerase binding site[43] | Oral administration | Liver | Fewer bone and kidney side effects, but can lead to dyslipidemia[52] | Low risk of drug resistance |
| TMF | 2021 | NtRTI | Competitive binding to HBV DNA polymerase binding site[56] | Oral administration | Liver | Fewer bone and kidney side effects[58] | Low risk of drug resistance, and effective against multiple drug-resistant HBV |
| INF-α | 1986 | Standard interferon | Regulate the immune response and induce the synthesis of antiviral proteins in host cells[87] | Subcutaneous injection | Kidney | More side effects: Systemic adverse reactions | No drug resistance |
| Peg-IFN-α | 2001 | Long-acting Interferon | Regulate the immune response and induce the synthesis of antiviral proteins in host cells[87] | subcutaneous injection | Liver and kidney | Similar to INF-α | No drug resistance |
NRTI: Nucleoside reverse transcriptase inhibitors, NtRTI: Nucleotide reverse transcriptase inhibitors; LAM: Lamivudine; ADV: Adefovir dipivoxil; ETV: Entecavir; LdT: Telbivudine; TDF: Tenofovir disoproxil fumarate; TAF: Tenofovir disoproxil fumarate; TMF: Tenofovir amibufenamide; IFN: Interferon; Peg-IFN-α: Polyethylene glycol interferon α; YMDD: Polymerase-tyrosine-methionine-aspartate; HBV: Hepatitis B virus.