Everything about Enfuvirtide totally explained
Enfuvirtide (
INN) is an
HIV fusion inhibitor, the first of a novel class of
antiretroviral drugs used in
combination therapy for the treatment of
HIV-1 infection. It is marketed under the trade name
Fuzeon (
Roche).
Enfuvirtide therapy costs an estimated USD$25,000 per year in the United States. Its cost and inconvenient dosing regimen are factors behind its use as a reserve, for "salvage" therapy in patients with multi-drug resistant HIV.
Structural formula
Ac-
Tyr-
Thr-
Ser-
Leu-
Ile-
His-Ser-Leu-
Ile-
Glu-Glu-Ser-
Gln-
Asn-Gln-Gln-Glu-
Lys-Asn-Glu-Gln-Glu-Leu-Leu-Glu-
Leu-
Asp-
Lys-
Trp-
Ala-Ser-Leu-Trp-
Asn-
Trp-
Phe-
NH2
History
Enfuvirtide originated at
Duke University, where researchers formed a pharmaceutical company known as Trimeris. Trimeris began development on enfuvirtide in
1996 and initially designated it
T-20. In 1999, Trimeris entered into partnership with
Hoffmann-La Roche to complete the development of the drug. It was approved by the U.S.
Food and Drug Administration (FDA) on
March 13,
2003 as the first HIV
fusion inhibitor, a new class of antiretroviral drugs. It was approved on the basis of two studies (TORO 1 and TORO 2) which compared the effect of optimized regimens of antiretroviral medication with and without the addition of enfuvirtide on serum
viral load.
Pharmacology
Mechanism of action
Enfuvirtide works by disrupting the
HIV-1 molecular machinery at the final stage of
fusion with the target
cell, preventing uninfected cells from becoming infected. A
biomimetic peptide, enfuvirtide was rationally designed to mimic components of the
HIV-1 fusion machinery and displace them, preventing normal fusion. Drugs that disrupt fusion of
virus and target
cell are termed
entry inhibitors or
fusion inhibitors.
HIV binds to the host CD4+ cell receptor via the viral protein GP120; upon binding, GP120 deforms allowing the viral protein GP41 to embed itself into the host cell's plasma membrane. Entry inhibitors bind to GP41 preventing the creation of an entry pore for the capsid of the virus, keeping it out of the cell.
Microbiology
Enfuvirtide is considered to be active against HIV-1 only. Low activity against HIV-2 isolates has been demonstrated
in vitro.
Variable susceptibility to enfuvirtide has been observed in clinical isolates, with acquired resistance the result of a mutated 10
amino acid motif in viral gp41. Primary resistance, however, has yet to be observed.
Clinical use
Indications
Enfuvirtide is indicated for the treatment of HIV-1 infection, in
combination therapy with other antiretrovirals, in patients where all other treatments have failed.
Dosage forms
By virtue of its peptide nature, enfuvirtide is marketed in injectable form. The lyophilised enfuvirtide powder must be reconstituted by the patient and administered twice daily by
subcutaneous injection.
Adverse effects
Common
adverse drug reactions (≥1% of patients) associated with enfuvirtide therapy include: injection site reactions (pain, hardening of skin,
erythema,
nodules,
cysts, itch; experienced by nearly all patients, particularly in the first week),
peripheral neuropathy,
insomnia,
depression, cough,
dyspnoea,
anorexia,
arthralgia, infections (including bacterial
pneumonia) and/or
eosinophilia. Various
hypersensitivity reactions occur infrequently (0.1–1% of patients), symptoms of which include rash, fever, nausea, vomiting, chills, rigors,
hypotension, elevated hepatic
transaminases; and possibly more severe reactions including
respiratory distress,
glomerulonephritis and/or
anaphylaxis –
rechallenge isn't recommended.
[Further Information]
Get more info on 'Enfuvirtide'.
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