Muromonab-CD3 (brand name Orthoclone OKT3, marketed by Janssen-Cilag) is an immunosuppressant medication given to reduce acute rejection in people with organ transplants.[1][2] It is a monoclonal antibody targeted at the CD3 receptor,[3] a membrane protein on the surface of T cells. It is the first monoclonal antibody to be approved for clinical use in humans.[2]
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Mouse |
| Target | CD3 |
| Clinical data | |
| Trade names | Orthoclone OKT3 |
| AHFS/Drugs.com | Consumer Drug Information |
| MedlinePlus | a605011 |
| Routes of administration | Intravenous |
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| Legal status | |
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| Identifiers | |
| CAS Number | |
| DrugBank | |
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| Chemical and physical data | |
| Formula | C6460H9946N1720O2043S56 |
| Molar mass | 146189.98 g·mol−1 |
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Medical uses
editMuromonab-CD3 is approved for the therapy of acute, glucocorticoid-resistant rejection of allogeneic kidney, heart, and liver transplants.[4] Unlike the monoclonal antibodies basiliximab and daclizumab, it is not approved for prophylaxis of transplant rejection, although a 1996 review has found it to be safe for that purpose.[5]
Contraindications
editExcept under special circumstances, the drug is contraindicated for patients with an allergy against mouse proteins, as well as patients with uncompensated heart failure, uncontrolled arterial hypertension or epilepsy. It should not be used during pregnancy or lactation.[2][4]
Adverse effects
editEspecially during the first infusion, the binding of muromonab-CD3 to CD3 can activate T cells to release cytokines like tumor necrosis factor and interferon gamma. This cytokine release syndrome, or CRS, includes side effects like skin reactions, fatigue, fever, chills, myalgia, headaches, nausea and diarrhea,[6] and could lead to life-threatening conditions like apnoea, cardiac arrest, and flash pulmonary edema.[4] To minimize the risk of CRS and to offset some of the minor side effects patient experience, glucocorticoids (such as methylprednisolone), acetaminophen, and diphenhydramine are given before the infusion.[7]
Other adverse effects include leucopenia, as well as an increased risk for severe infections and malignancies typical of immunosuppressive therapies. Neurological side effects like aseptic meningitis and encephalopathy have been observed. Possibly, they are also caused by the T cell activation.[4]
Repeated application can result in tachyphylaxis (reduced effectiveness) due to the formation of anti-mouse antibodies in the patient, which accelerates elimination of the drug. It can also lead to an anaphylactic reaction against the mouse protein,[2] which may be difficult to distinguish from a CRS.
Pharmacology
editT cells recognise antigens primarily via the T cell receptor (TCR).[8]: 160 CD3 is one of the proteins that make up the TCR complex.[8]: 166 The TCR transduces the signal for the T cell to proliferate and attack the antigen.[8]: 160
Muromonab-CD3 is a murine (mouse) monoclonal IgG2a antibody which was created using hybridoma technology.[9] It binds to the T cell receptor-CD3-complex (specifically the CD3 epsilon chain) on the surface of circulating T cells, initially leading to an activation,[7] but subsequently inducing the clearance of TCR complex from cell surface and apoptosis of the T cells.[10] This protects the transplant against the T cells.[2][4] When administered for transplant induction, the drug is administered daily thereafter for up to 7 days.[7]
Newer monoclonal antibodies in development with the same mechanism of action include otelixizumab (also known as TRX4), teplizumab (also known as hOKT3γ1(Ala-Ala) ), visilizumab and foralumab. They are being investigated for the treatment of other conditions like Crohn's disease, ulcerative colitis, and type 1 diabetes.
History
editMuromonab-CD3 was approved by the U.S. Food and Drug Administration (FDA) in 1986,[5] making it the first monoclonal antibody to be approved anywhere as a drug for humans. In the European Communities, it is the first drug to be approved under the directive 87/22/EWG, a precursor of the European Medicines Agency (EMA) centralised approval system in the European Union. This process included an assessment by the Committee for Proprietary Medicinal Products (CPMP, now CHMP), and a subsequent approval by the national health agencies; in Germany, for example, in 1988 by the Paul Ehrlich Institute in Frankfurt. However, the manufacturer of muromonab-CD3 has voluntarily withdrawn[11] it from the United States market in 2010 due to numerous side-effects, better-tolerated alternatives and declining usage.[12]
Society and culture
editLegal status
editOrthoclone OKT3 was withdrawn from the US market in 2010.[13]
Etymology
editMuromonab-CD3 was developed before the WHO nomenclature of monoclonal antibodies took effect, and consequently its name does not follow this convention. Instead, it is a contraction from "murine monoclonal antibody targeting CD3".[2]
Research
editIt has also been investigated for use in treating T-cell acute lymphoblastic leukemia.[14]
References
edit- ^ Midtvedt K, Fauchald P, Lien B, Hartmann A, Albrechtsen D, Bjerkely BL, et al. (February 2003). "Individualized T cell monitored administration of ATG versus OKT3 in steroid-resistant kidney graft rejection". Clinical Transplantation. 17 (1): 69–74. doi:10.1034/j.1399-0012.2003.02105.x. PMID 12588325. S2CID 8677441.
- ^ a b c d e f Mutschler E, Geisslinger G, Kroemer HK, Schäfer-Korting M (2001). Arzneimittelwirkungen (in German) (8 ed.). Stuttgart: Wissenschaftliche Verlagsgesellschaft. p. 937. ISBN 3-8047-1763-2.
- ^ "muromonab-CD3". Guide to Pharmacology. IUPHAR/BPS. Retrieved 21 August 2015.
- ^ a b c d e "Orthoclone OKT3". Professional Drug Information. Drugs.com. Archived from the original on 3 March 2016. Retrieved 3 January 2010.
- ^ a b Smith SL (September 1996). "Ten years of Orthoclone OKT3 (muromonab-CD3): a review". Journal of Transplant Coordination. 6 (3): 109–119, quiz 119–1. doi:10.7182/prtr.1.6.3.8145l3u185493182. PMID 9188368.
- ^ Abramowicz D, Schandene L, Goldman M, Crusiaux A, Vereerstraeten P, De Pauw L, et al. (April 1989). "Release of tumor necrosis factor, interleukin-2, and gamma-interferon in serum after injection of OKT3 monoclonal antibody in kidney transplant recipients". Transplantation. 47 (4): 606–608. doi:10.1097/00007890-198904000-00008. PMID 2523100. S2CID 22740065.
- ^ a b c Bhorade SM, Stern E (January 2009). "Immunosuppression for lung transplantation". Proceedings of the American Thoracic Society. 6 (1): 47–53. doi:10.1513/pats.200808-096go. PMID 19131530.
- ^ a b c Rich R (2013). Clinical immunology : principles and practice (4th ed.). London: Elsevier. ISBN 978-0-7234-3710-9. OCLC 823736017.
- ^ Sgro C (December 1995). "Side-effects of a monoclonal antibody, muromonab CD3/orthoclone OKT3: bibliographic review". Toxicology. Immunotoxicology Papers presented at the Third Summer School in Immunotoxicology. 105 (1): 23–29. Bibcode:1995Toxgy.105...23S. doi:10.1016/0300-483X(95)03123-W. PMID 8638282.
- ^ Benekli M, Hahn T, Williams BT, Cooper M, Roy HN, Wallace P, et al. (September 2006). "Muromonab-CD3 (Orthoclone OKT3), methylprednisolone and cyclosporine for acute graft-versus-host disease prophylaxis in allogeneic bone marrow transplantation". Bone Marrow Transplantation. 38 (5): 365–370. doi:10.1038/sj.bmt.1705450. PMID 16862164. S2CID 31056997.
- ^ Abdi R, Martin S, Gabardi S (2009). "Immunosuppressive Strategies in Human Renal Transplantation – Induction Therapy" (PDF). Nephrology Rounds. 7 (4). Retrieved 11 November 2012.[permanent dead link]
- ^ Mahmud N, Klipa D, Ahsan N (2010). "Antibody immunosuppressive therapy in solid-organ transplant: Part I". mAbs. 2 (2): 148–156. doi:10.4161/mabs.2.2.11159. PMC 2840233. PMID 20150766.
- ^ "Drug Record: Muromonab-CD3". Livertox: Clinical and Research Information on Drug-Induced Liver Injury. National Institute of Diabetes and Digestive and Kidney Diseases. 2012. PMID 31643905.
- ^ Gramatzki M, Burger R, Strobel G, Trautmann U, Bartram CR, Helm G, et al. (March 1995). "Therapy with OKT3 monoclonal antibody in refractory T cell acute lymphoblastic leukemia induces interleukin-2 responsiveness". Leukemia. 9 (3): 382–390. PMID 7885036.
