Alefacept

Alefacept

Systematic (IUPAC) name
1-92-LFA-3 (Antigen) (human) fusion protein with immunoglobin G1 (human hinge CH2-CH3γ1-chain) dimer
Clinical data
AHFS/Drugs.com	monograph
MedlinePlus	a603011
Pregnancy cat.	C(AU) B(US)
Legal status	℞-only (US)
Routes	Intravenous, intramuscular
Pharmacokinetic data
Bioavailability	63% (IM)
Half-life	~270 hours
Identifiers
CAS number	222535-22-0 Y
ATC code	L04AA15
DrugBank	BTD00055
UNII	ELK3V90G6C Y
KEGG	D02800 Y
ChEMBL	CHEMBL1201571 N
Chemical data
Formula	C2306H3594N610O694S26
Mol. mass	51801.1 g/mol
N(what is this?)  (verify)

Alefacept is a genetically engineered immunosuppressive drug sold under the brand name Amevive in Canada, the United States, Israel, Switzerland and Australia. It is used to control inflammation in moderate to severe psoriasis with plaque formation, where it interferes with lymphocyte activation.^[1] It is also being studied in the treatment of cutaneous T-cell lymphoma and T-cell non-Hodgkin lymphoma.

Alefacept is a fusion protein: it combines part of an antibody with a protein that blocks the growth of some types of T cells.

Contents 1 Mode of action 2 Drawbacks 3 Indications 4 Contraindications and precautions 5 Pregnancy and lactation 6 Pediatric patients 7 Side effects 8 Interactions 9 Necessary laboratory examinations 10 Dosage regimes 11 Notes 12 External links

Mode of action

The exact mode of action is very complicated and involves dual mechanisms, one of which inhibits the activation of CD4⁺ and CD8⁺ T cells by interfering with CD2 on the T cell membrane thereby blocking the costimulatory molecule LFA-3/CD2 interaction. The second mechanism is inducing apoptosis of memory-effector T lymphocytes. If the T cells were to become activated they would stimulate proliferation of keratinocytes resulting in the typical psoriatic symptoms. Therefore, alefacept leads to clinical improvement of moderate to severe psoriasis by blunting these reactions.Combinations of therapeutic modalities have been utilized to meet the challenge of difficult to treat psoriasis.^[2]

Drawbacks

Due to safety issues (immunosuppression, risk of infections, malignancies, and allergies) the European Medicines Agency (EMEA) has so far rejected to approve alefacept.

Indications

Alefacept is indicated for the management of patients with moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy or phototherapy. The concomitant use of low-potency topical corticosteroids was permitted during the treatment phase with alefacept and does not seem to pose any additional risks.

The drug was approved based upon studies involving 1,869 patients altogether with plaques covering at least 10% of body surface. Either 7.5 mg IV or 15 mg IM once a week were applied. The long term results (reduction of at least 75% in pretreatment PASI scores) were 14% and 21%, respectively. Additional improvements ensuing after completion of the 12-week treatment phase or after completion of a second alefacept treatment were also seen. Often the remissions were maintained for 7 to 12 months after end of treatment.

Contraindications and precautions

• Alefacept reduces CD4⁺ T cell counts and may worsen the clinical course of HIV infections. It is therefore contraindicated in patients with HIV infections.
• Pretreatment CD4⁺ and/or CD8⁺ cell counts below the accepted lower limit
• History of systemic malignancy
• Caution: Patients at high risk to develop a systemic malignancy
• Known hypersensitivity to alefacept or to any other ingredient of the preparation
• Caution: There is little experience in geriatric patients (65 years of age or older); so far no differences to the younger age group have been noted.

Pregnancy and lactation

• Alefacept has been assigned to Pregnancy Category B in the US and to C in Australia.
• Lactation : It is not known if the drug is excreted into human milk. Either the drug or breastfeeding should be terminated, taking into account the importance of treatment to the mother.

Pediatric patients

No clinical experience exists in patients under 18 years of age. The drug should therefore not be used in pediatric patients.

Side effects

• Lymphopenia : Most common in clinical trials was a significant and dose-related reduction of CD4+ and CD8+ counts in 10 to 59% of patients. However, only 0 to 2% of patients experienced reductions below the accepted lower limit. Consequences of lymphopenia may be infections and/or treatment related malignancies (see below).
• Malignancies : In clinical studies among 1,869 patients 63 treatment-emerged malignancies in 43 patients were observed. Most of these were nonmelanoma and melanoma skin cancers, other solid tumors, and lymphomas.
• Infections : In clinical studies 0.9% of patients experienced significant infections compared to 0.2% in the placebo group. Among the infections were serious ones such as sepsis, pneumonia, abscesses, wound infections and toxic shock syndrome.
• Sensitivity reactions: Urticaria and angioedema were observed. If an anaphylactic reaction should occur symptomatic treatment should be initiated at once.
• Forming of antibodies to alefacept : About 3% of patients developed low-titer antibodies with unknown importance for the clinical efficiency of the drug. Long-term immune effects have not been well explored.
• Hepatic Toxicity : Postmarketing reports revealed asymtomatic increases in transaminases (ALT and/or AST), fatty liver degeneration, decompensation of preexisting liver cirrhosis, and acute treatment-related liver failure. It is not known if some or all of these manifestations are attributable to alefacept-therapy, but it is recommended to discontinue therapy as soon as any sign of liver toxicity develops.
• Different Common Side Effects : side effects such as pharyngitis, cough, dizziness, nausea, pruritus, myalgias, chills, and reactions at injection sites were observed quite frequently.

Interactions

• Patients currently undergoing immunosuppressive therapy (phototherapy, or concomitant application of other immunosuppressant agents) should not receive alefacept in order to avoid the risks of excessive immunosuppression. Studies concerning the combination with cyclosporine or methotrexate are conducted, but no results have been published so far.
• Live vaccines : The efficiency of concomitant application of live vaccines has not been fully examined yet. However, the effect of tetanus toxoid was well preserved in clinical trials.

Necessary laboratory examinations

• CD4⁺ cell counts should be obtained before initiation of therapy and during the 12-week course of therapy in intervals of 2 weeks.
• It may be desirable to monitor liver function studies (AST and ALT) in patients at high risk to develop liver toxicity (e.g., preexisting hepatitis, or high daily consumption of alcohol).

Dosage regimes

The standard dosage regime is the weekly application of either 7.5 mg IV or 15 mg IM for a course of 12 weeks. The benefits and risks of repeated courses have not been explored in sufficient detail. Therapy should be conducted under the supervision of a physician experienced in the use of immunosuppressant agents.

Notes

 This article incorporates public domain material from the U.S. National Cancer Institute document "Dictionary of Cancer Terms".

External links

• Koo J, Bagel J, Sweetser M, Ticho B (2006). "Alefacept in combination with ultraviolet B phototherapy for the treatment of chronic plaque psoriasis: results from an open-label, multicenter study.". J Drugs Dermatol 5 (7): 623–8. PMID 16865867. 
• Krell J (2006). "Use of alefacept and etanercept in 3 patients whose psoriasis failed to respond to etanercept.". J Am Acad Dermatol 54 (6): 1099–101. doi:10.1016/j.jaad.2005.08.032. PMID 16713481. 
• Parrish C, Sobera J, Robbins C, Cantrell W, Desmond R, Elewski B (2006). "Alefacept in the treatment of psoriatic nail disease: a proof of concept study.". J Drugs Dermatol 5 (4): 339–40. PMID 16673801. 
• AHFS Database online

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