Alefacept je korišten za kontrolisanje inflamacije pri umerenoj do jake psorijaze sa formiranjem plakova. On ometa aktivaciju limfocita.[3] Alefacept je imunosupresivni dimerni fuzioni protein koji se sastoji od ekstracelularne CD2-vezujuće porcije ljudskog leukocnog funkcionog antigena-3 (LFA-3) vezanog za Fc (zglobin, CH2 i CH3 domain) porciju ljudskog IgG1.[4][5][6][7][8]
- ↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
- ↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
- ↑ „New drugs”. Australian Prescriber 27 (101): 5. 2004. Arhivirano iz originala na datum 2006-08-24. Pristupljeno 2006-08-20.
- ↑ Koo JY, Bagel J, Sweetser MT, Ticho BS: Alefacept in combination with ultraviolet B phototherapy for the treatment of chronic plaque psoriasis: results from an open-label, multicenter study. J Drugs Dermatol. 2006 Jul-Aug;5(7):623-8. PMID 16865867
- ↑ Krell JM: Use of alefacept and etanercept in 3 patients whose psoriasis failed to respond to etanercept. J Am Acad Dermatol. 2006 Jun;54(6):1099-101. PMID 16713481
- ↑ Parrish CA, Sobera JO, Robbins CM, Cantrell WC, Desmond RA, Elewski BE: Alefacept in the treatment of psoriatic nail disease: a proof of concept study. J Drugs Dermatol. 2006 Apr;5(4):339-40. PMID 16673801
- ↑ Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035-41. DOI:10.1093/nar/gkq1126. PMC 3013709. PMID 21059682. edit
- ↑ David S. Wishart, Craig Knox, An Chi Guo, Dean Cheng, Savita Shrivastava, Dan Tzur, Bijaya Gautam, and Murtaza Hassanali (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Res 36 (Database issue): D901-6. DOI:10.1093/nar/gkm958. PMC 2238889. PMID 18048412. edit
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Intracelularni (inicijacija) | |
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Intracelularni (recepcija) | |
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Ekstracelularni | | | Serum cilj (non-celularni) | |
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Celularni ciljevi | CD3 ( Muromonab-CD3, Oteliksizumab, Teplizumab, Visilizumab) • CD4 ( Klenoliksimab, Keliksimab, Zanolimumab) • CD11a ( Efalizumab) • CD18 ( Erlizumab) • CD20 ( Afutuzumab, Ocrelizumab, Pascolizumab) • CD23 ( Lumiliksimab) • CD40 ( Teneliksimab, Toralizumab) • CD62L/L-selektin ( Aselizumab) • CD80 ( Galiksimab) • CD147/Basigin ( Gavilimomab) • CD154 ( Ruplizumab)
BLyS (Belimumab) • CTLA-4 (Ipilimumab, Tremelimumab) • CAT (Bertilimumab, Lerdelimumab, Metelimumab) • Integrin (Natalizumab) • Interleukin-6 receptor (Tocilizumab) • LFA-1 (Odulimomab)
IL-2 receptor/CD25 (Basiliksimab, Daklizumab, Inolimomab)
T-limfocit ( Zolimomab aritoks) |
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Nesortirani | Atorolimumab, Cedelizumab, Dorliksizumab, Fontolizumab, Gantenerumab, Gomiliksimab, Maslimomab, Morolimumab, Pekselizumab, Reslizumab, Rovelizumab, Siplizumab, Talizumab, Telimomab aritoks, Vapaliksimab, Vepalimomab |
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