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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/07/17 03:07:33」(JST)
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Visilizumab?
Monoclonal antibody |
Type |
Whole antibody |
Source |
Humanized (from mouse) |
Target |
CD3 receptor |
Identifiers |
CAS Registry Number |
Y |
ATC code |
None |
|
Y (what is this?) (verify) |
Visilizumab (tentative trade name Nuvion, PDL BioPharma Inc.) is a humanized monoclonal antibody. It is being investigated for use as an immunosuppressive drug in patients with ulcerative colitis and Crohn's disease. Visilizumab binds to the CD3 receptor on certain activated T cells without affecting resting T cells. It is currently under clinical studies for the treatment of ulcerative colitis and Crohn's disease.[1]
PDL BioPharma, Inc. canceled production of visilizumab following its Phase II/III clinical trials, citing its inefficacy and poor safety profile compared to other drugs on the market as the major reasons.[2] Nevertheless, clinical trials continue for various diseases like multiple myeloma[3] and diabetes mellitus type 1[4][5] as of July 2009[update].
Visilizumab has also been radiolabelled with technetium-99m for imaging T cells.[6]
References
- ^ "PDL BioPharma, Development Pipeline - Nuvion (visilizumab)". Archived from the original on 2007-09-15. Retrieved 2008-02-11.
- ^ "PDL Lands in a Hazard". Retrieved 2009-05-27.
- ^ "Treated T Cells Followed by a Stem Cell Transplant in Treating Patients With Multiple Myeloma". ClinicalTrials.gov. Retrieved 2010-03-15.
- ^ Kaufman, A; Herold, KC (2009). "Anti-CD3 mAbs for treatment of type 1 diabetes". Diabetes/metabolism research and reviews 25 (4): 302–6. doi:10.1002/dmrr.933. PMID 19319985.
- ^ "Anti-CD3 mAb Treatment of Recent Onset Type 1 Diabetes". ClinicalTrials.gov.
- ^ Malviya, G; D'alessandria, C; Bonanno, E; Vexler, V; Massari, R; Trotta, C; Scopinaro, F; Dierckx, R; Signore, A (2009). "Radiolabeled Humanized Anti-CD3 Monoclonal Antibody Visilizumab for Imaging Human T-Lymphocytes". Journal of Nuclear Medicine 50 (10): 1683–91. doi:10.2967/jnumed.108.059485. PMID 19759100.
Immunosuppressive drugs / Immunosuppressants (L04)
|
|
Intracellular
(initiation) |
Antimetabolites |
- purine synthesis inhibitors: Azathioprine
- Mycophenolic acid
- pyrimidine synthesis inhibitors: Leflunomide
- Teriflunomide
|
|
Macrolides/
other IL-2 inhibitors |
- FKBP/Cyclophilin/Calcineurin: Tacrolimus
- Ciclosporin
- Pimecrolimus
|
|
IMiDs |
- Lenalidomide
- Pomalidomide
- Thalidomide
|
|
|
Intracellular
(reception) |
IL-1 receptor antagonists |
|
|
mTOR |
- Sirolimus
- Everolimus
- Ridaforolimus
- Temsirolimus
- Umirolimus
- Zotarolimus
|
|
|
Extracellular |
Antibodies |
Monoclonal |
Serum target
(noncellular) |
- Complement component 5 (Eculizumab)
- TNF (Adalimumab
- Afelimomab
- Certolizumab pegol
- Golimumab
- Infliximab
- Nerelimomab)
- Interleukin 5 (Mepolizumab)
- Immunoglobulin E (Omalizumab)
- IL-12 and IL-23 (Lebrikizumab
- Ustekinumab)
|
|
Cellular target |
- CD3 (Muromonab-CD3
- Otelixizumab
- Teplizumab
- Visilizumab)
- CD4 (Clenoliximab
- Keliximab
- Zanolimumab)
- CD11a (Efalizumab)
- CD18 (Erlizumab)
- CD20 (Obinutuzumab
- Rituximab
- Ocrelizumab
- Pascolizumab)
- CD23 (Gomiliximab
- Lumiliximab)
- CD40 (Teneliximab
- Toralizumab)
- CD62L/L-selectin (Aselizumab)
- CD80 (Galiximab)
- CD147/Basigin (Gavilimomab)
- CD154 (Ruplizumab)
- BLyS (Belimumab
- Blisibimod)
- CTLA-4 (Ipilimumab
- Tremelimumab)
- CAT (Bertilimumab
- Lerdelimumab
- Metelimumab)
- Integrin (Natalizumab)
- Interleukin-6 receptor (Tocilizumab)
- LFA-1 (Odulimomab)
- IL-2 receptor/CD25 (Basiliximab
- Daclizumab
- Inolimomab)
- T-lymphocyte (Zolimomab aritox)
|
|
Unsorted |
- Atorolimumab
- Cedelizumab
- Fontolizumab
- Maslimomab
- Morolimumab
- Pexelizumab
- Reslizumab
- Rovelizumab
- Siplizumab
- Talizumab
- Telimomab aritox
- Vapaliximab
- Vepalimomab
|
|
|
Polyclonal |
- Anti-thymocyte globulin
- Anti-lymphocyte globulin
|
|
|
-cept (Fusion) |
- CTLA-4 (Abatacept
- Belatacept)
- TNF inhibitor (Etanercept
- Pegsunercept)
- Aflibercept
- Alefacept
- Rilonacept
|
|
|
Index of the immune system
|
|
Description |
- Physiology
- cells
- autoantigens
- autoantibodies
- complement
- surface antigens
- IG receptors
|
|
Disease |
- Allergies
- Immunodeficiency
- Immunoproliferative immunoglobulin disorders
- Hypersensitivity and autoimmune disorders
- Neoplasms and cancer
|
|
Treatment |
- Procedures
- Drugs
- antihistamines
- immunostimulants
- immunosuppressants
- monoclonal antibodies
|
|
|
UpToDate Contents
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English Journal
- Visilizumab with tacrolimus and methotrexate for GvHD prevention after allogeneic hematopoietic cell transplantation from mismatched unrelated donors.
- Perez LE1,2, Fernandez H1,2, Ayala E1,2, Beato F1, Neuger A3, Pidala J1,2, Schell MJ4, Anasetti C1,2.
- Bone marrow transplantation.Bone Marrow Transplant.2016 Dec 19. doi: 10.1038/bmt.2016.330. [Epub ahead of print]
- PMID 27991896
- Therapeutic anti-CD3 monoclonal antibodies: from bench to bedside.
- Kuhn C1, Weiner HL1.
- Immunotherapy.Immunotherapy.2016 Jul;8(8):889-906. doi: 10.2217/imt-2016-0049. Epub 2016 May 10.
- The induction of tolerance is a major goal of immunotherapy. Investigations over the last 20 years have shown that anti-CD3 monoclonal antibodies (mAbs) effectively treat autoimmune disease in animal models and have also shown promise in clinical trials. Tolerance induction by anti-CD3 mAbs is relat
- PMID 27161438
- Heterogeneous CD3 expression levels in differing T cell subsets correlate with the in vivo anti-CD3-mediated T cell modulation.
- Valle A1, Barbagiovanni G1, Jofra T2, Stabilini A2, Perol L3, Baeyens A4, Anand S5, Cagnard N6, Gagliani N2, Piaggio E7, Battaglia M8.
- Journal of immunology (Baltimore, Md. : 1950).J Immunol.2015 Mar 1;194(5):2117-27. doi: 10.4049/jimmunol.1401551. Epub 2015 Feb 2.
- The tolerogenic anti-CD3ε monoclonal Abs (anti-CD3) are promising compounds for the treatment of type 1 diabetes. Anti-CD3 administration induces transient T cell depletion both in preclinical and in clinical studies. Notably, the said depletion mainly affects CD4(+) but not CD8(+) T cells. Moreove
- PMID 25646305
Related Links
- 1. Clin Immunol. 2008 Jun;127(3):322-9. doi: 10.1016/j.clim.2008.02.009. Visilizumab induces apoptosis of mucosal T lymphocytes in ulcerative colitis through activation of caspase 3 and 8 dependent pathways. Yu QT(1 ...
- 海外で流れていた新薬の開発状況に関する情報です。visilizumabは最近盛んに開発がされている「生物学的製剤」の一つです。「T細胞」は幾つかの種類があ...
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