:''For a list of immunosuppressive drugs, see the
transplant rejection page''.
'Immunosuppressive drugs' or 'immunosuppressants' are
drugs that are used in
immunosuppressive therapy to inhibit or prevent activity of the
immune system. Clinically they are used to:
★ prevent the
rejection of
transplanted organs and tissues (e.g.
bone marrow,
heart,
kidney,
liver)
★ treatment of
autoimmune diseases or diseases that are most likely of autoimmune origin (e.g.
rheumatoid arthritis,
myasthenia gravis,
systemic lupus erythematosus,
Crohn's disease, and
ulcerative colitis).
★ treatment of some other non-autoimmune inflammatory diseases (eg. long term Allergic
Asthma control).
These drugs are not without
side effects and risks. Because the majority of them act non-selectively, the immune system loses its ability to successfully resist
infections and spreading of
malignant cells. There are also other side effects, like
hypertension,
dyslipidemia,
hyperglycemia,
peptic ulcers, liver and kidney injury. The immunosuppressive drugs also interact with other medicines and affect their
metabolism and action.
Immunosuppressive drugs can be classified into five groups:
★
glucocorticoids
★
cytostatics
★
antibodies
★
drugs acting on immunophilins
★
other drugs
Glucocorticoids
''General information:
Glucocorticoid.''
In pharmacologic (supraphysiologic) doses, glucocorticoids are used to suppress various
allergic,
inflammatory, and autoimmune disorders. They are also administered as posttransplantory immunosuppressants to prevent the
acute transplant rejection and
graft-versus-host disease. Nevertheless, they do not prevent an infection and also inhibit later
reparative processes.
Immunosuppressive mechanism
Glucocorticoids suppress the
cell-mediated immunity. They act by inhibiting genes that code for the cytokines
IL-1,
IL-2,
IL-3,
IL-4,
IL-5,
IL-6,
IL-8 and TNF-γ, the most important of which is the IL-2. Smaller
cytokine production reduces the
T cell proliferation.
Glucocorticoids also suppress the
humoral immunity, causing
B cells to express smaller amounts of IL-2 and of
IL-2 receptors. This diminishes both B cell clone expansion and
antibody synthesis.
Antiinflammatory effects
Glucocorticoids influence all types of inflammatory events, no matter what their cause. They induce the
lipocortin-1 (annexin-1) synthesis, which then binds to
cell membranes preventing the
phospholipase A2 from coming into contact with its
substrate arachidonic acid. This leads to diminished
eicosanoid production. The
cyclooxygenase (both COX-1 and COX-2) expression is also suppressed, potentiating the effect.
Glucocorticoids also stimulate the lipocortin-1 escaping to the extracellular space, where it binds to the
leukocyte membrane receptors and inhibits various inflammatory events:
epithelial adhesion,
emigration,
chemotaxis,
phagocytosis,
respiratory burst and the release of various inflammatory mediators (lysosomal enzymes, cytokines,
tissue plasminogen activator,
chemokines etc.) from
neutrophils,
macrophages and
mastocytes.
Cytostatics
''General information:
Chemotherapy''
Cytostatics inhibit
cell division. In immunotherapy, they are used in smaller doses than in the treatment of malignant diseases. They affect the proliferation of both T cells and B cells. Due to their highest effectiveness,
purine analogs are most frequently administered.
Alkylating agents
The
alkylating agents used in immunotherapy are
nitrogen mustards (cyclophosphamide),
nitrosoureas,
platinum compounds and others. Cyclophosphamide is probably the most potent immunosuppressive compound. In small doses, it is very efficient in the therapy of
systemic lupus erythematosus, autoimmune
hemolytic anemias,
Wegener's granulomatosis and other immune diseases. High doses cause
pancytopenia and hemorrhagic
cystitis.
Antimetabolites
Antimetabolites interfere with the synthesis of nucleic acids. These include:
★
folic acid analogues, such as
methotrexate
★
purine analogues such as
azathioprine and
mercaptopurine
★
pyrimidine analogues
★
protein synthesis inhibitors.
Methotrexate
Methotrexate is a
folic acid analogue. It binds
dihydrofolate reductase and prevents synthesis of
tetrahydrofolate. It is used in the treatment of autoimmune diseases (for example rheumatoid arthritis) and in transplantations.
Azathioprine and Mercaptopurine
Azathioprine, is the main immunosuppressive cytotoxic substance. It is extensively used to control transplant rejection reactions. It is nonenzymatically cleaved to
mercaptopurine, that acts as a purine analogue and an inhibitor of DNA synthesis. Mercaptopurine itself can also be administered directly.
By preventing the clonal expansion of lymphocytes in the induction phase of the immune response, it affects both the
cell and the
humoral immunity. It is also efficient in the treatment of autoimmune diseases.
Cytotoxic antibiotics
Among these,
dactinomycin is the most important. It is used in
kidney transplantations. Other cytotoxic antibiotics are
anthracyclines,
mitomycin C,
bleomycin,
mithramycin.
Antibodies
Antibodies are used as a quick and potent immunosuppression method to prevent the acute rejection reaction.
Polyclonal antibodies
Heterologous
polyclonal antibodies are obtained from the
serum of animals (e.g.
rabbit,
horse) and injected with the patient's
thymocytes or lymphocytes. The antilymphocyte (ALG) and antithymocyte
antigens (ATG) are being used. They are part of the steroid-resistant acute rejection reaction and grave
aplastic anemia treatment. However, they are primarily added to other immunosuppressives to diminish their dosage and toxicity. They also allow transition to cyclosporine therapy.
''
Polyclonal antibodies inhibit T lymphocytes and cause their
lysis, which is both
complement mediated cytolysis and cell-mediated
opsonization followed by removal of
reticuloendothelial cells from the
circulation in the
spleen and liver]]''. In this way, polyclonal antibodies inhibit cell-mediated immune reactions, including graft rejection,
delayed hypersensitivity (i.e.
tuberculin skin reaction), and the
graft-versus-host disease (GVHD), but influence
thymus-dependent antibody production.
Currently (
March 2005) there are two preparations available to the market: Atgam (R), obtained from horse serum, and ''
Thymoglobuline (R), obtained from rabbit serum.''Polyclonal antibodies affect all lymphocytes and cause general immunosuppression possibly leading to
post-transplant lymphoproliferative disorders (PTLD) or serious infections, especially by
cytomegalovirus. To reduce these risks, treatment is provided in a hospital where adequate isolation from infection is available. They are usually administered for five days intravenously in the appropriate quantity. Patients stay in the hospital as long as three weeks to give the immune system time to recover to a point where there is no longer a risk of
serum sickness.
Because of a high
immunogenicity of polyclonal antibodies, almost all patients have an acute reaction to the treatment. It is characterized by
fever,
rigor episodes and even
anaphylaxis. Later during the treatment, some patients develop serum sickness or
immune complex glomerulonephritis. Serum sickness arises seven to fourteen days after the therapy has begun. The patient suffers from fever,
joint pain and
erythema that can be soothed with the use of steroids and
analgesics.
Urticaria (hives) can also be present. It is possible to diminish their toxicity by using highly purified
serum fractions and intravenous administration in the combination with other immunosuppressants, for example
calcineurin inhibitors, cytostatics and cortisteroids. The most frequent combination is to simultaneously use antibodies and cyclosporine. Patients gradually develop a strong immune response to these drugs, reducing or eliminating their effectiveness.
Monoclonal antibodies
Monoclonal antibodies are directed towards exactly defined antigens. Therefore, they cause fewer side effects. Especially significant are the
IL-2 receptor (CD25) and CD3 directed antibodies. They are used to prevent the rejection of transplanted organs, but also to track changes in the lymphocyte subpopulations. It is reasonable to expect similar new drugs in the future.
T-cell receptor directed antibodies
OKT3 (R) is presently the only approved anti-CD3 antibody. It is a mouse anti-CD3 monoclonal antibody of the IgG2a type that prevents
T-cell activation and proliferation by binding the T-cell receptor complex present on all differentiated T cells. As such, it is one of the most potent immunosuppressive substances and is clinically used to control the steroid and/or polyclonal antibodies resistant acute rejection episodes. For acting more specifically than polyclonal antibodies, it is also used preventively in transplantations.
Presently, the OKT3's action mechanism is not yet sufficiently understood. It is known that the molecule binds TCR/CD3, the T-cell receptor complex. During the first few administrations, this binding non-specifically activates T cells, leading to a serious syndrome 30 to 60 minutes later. It is characterized by fever, myalgia, headache and artralgia. In some cases, it progresses to a life-threatening reaction of the cardiovascular system and the central nervous system needing a lengthy therapy. Past this period, CD3 (R) blocks the TCR - antigen binding and causes conformation change or the removal of the entire TCR3/CD3 from the T-cell surface. This lowers the number of T cells, perhaps by sensitising them for the uptake by the reticular epithelial cells. The cross-binding of CD3 molecules also activates an intracellular signal, causing the T cells' anergy or apoptosis, unless they receive another signal through a costimulatory molecule. CD3 antibodies also shift the balance from Th1 to Th2 cells.
Deciding whether to use OKT3(R) in the treatment, it is therefore necessary not only to consider its great effectiveness, but also its toxic side effects: the risk of excessive immunosuppression and the risk that the patient develops neutralizing antibodies against the drug, making it inefficacious. Although CD3(R) antibodies act more specifically than polyclonal antibodies, they lower the cell-mediated immunity significantly, predisposing the patient to opportunistic infections and malignancies.
IL-2 receptor directed antibodies
Interleukin-2 is an important immune system regulator necessary for the clone expansion and survival of activated lymphocytes T. Its effects are mediated by the trimer cell surface receptor IL-2a, consisting of the α, β and γ chains. The IL-2a (CD25, T-cell activation antigen, TAC) is expressed only by the already activated T lymphocytes. Therefore, it is of special significance to the selective immunosuppressive treatment and the research has been focused on the development of effective and safe anti-IL-2 antibodies. By the use of the recombinant gene technology, the mouse anti-Tac antibodies have been modified leading to the presentation of two himeric mouse/human anti-Tac antibodies in the year 1998: basiliximab (Simulect (R)) and daclizumab (Zenapax (R)). These drugs act by binding the IL-2a receptor's α chain, preventing the IL-2 induced clonal expansion of activated lymphocytes and shortening their survival. They are used in the prophylaxis of the acute organ rejection after the bilateral kidney transplantation, both being similarly effective and with only few side effects.
Drugs acting on immunophilins
Cyclosporin
''General information:
cyclosporin''
Together with
tacrolimus,
cyclosporin is a
calcineurin inhibitor. It has been in use since
1983 and is one of the most widely used immunosuppressive drugs. It is a fungal peptide, composed of 11 amino acids.
Cyclosporin is thought to bind to the cytosolic protein
cyclophilin (an immunophilin) of immunocompetent lymphocytes, especially
T-lymphocytes. This complex of cyclosporin and cyclophilin inhibits
calcineurin, which under normal circumstances induces the transcription of
interleukin-2. The drug also inhibits
lymphokine production and
interleukin release, leading to a reduced function of effector T-cells.
Cyclosporin is used in the treatment of acute rejection reactions, but has been increasingly substituted with newer immunosuppressants, as it is
nephrotoxic.
Tacrolimus (Prograf(TM), FK506)
Tacrolimus is a fungal product (''
Streptomyces tsukubaensis''). It is a
macrolide lactone and acts by inhibiting
calcineurin.
The drug is used particularly in the liver and kidney transplantations, although in some clinics it is used in heart, lung and heart/lung transplants. It binds to an immunophilin, followed by the binding of the complex to calcineurin and the inhibition of its phosphatase activity. In this way, it prevents the passage of G0 into G1 phase. Tacrolimus is more potent than cyclosporin and has less pronounced side effects.
Sirolimus (Rapamune (Tm), Rapamycin)
Sirolimus is a macrolide lactone, produced by the
actinomycetes ''
Streptomyces hygroscopicus''. It is used to prevent rejection reactions. Although it is a structural analogue of tacrolimus, it acts somewhat differently and has different side effects.
Contrary to cyclosporine and tacrolimus that affect the first phase of the T lymphocyte activation, sirolimus affects the second one, namely the signal transduction and their clonal proliferation. It binds to the same receptor (immunophilin) as tacrolimus, however the produced complex does not inhibit calcineurin, but another protein. Therefore, sirolimus acts synergistically with cyclosporine and, in combination with other immunosuppressants, has few side effects. Indirectly it inhibits several T lympohocyte kinases and phosphatases, preventing the transmission of signal into their activity and the transition of the cell cycle from G1 to S phase. Similarly, it prevents the B cell differentiation to the plasma cells, which lowers the quantity of IgM, IgG and IgA antibodies produced. It acts as an immunoregulatory agent, and is also active against tumors that involve the PI3K/AKT/mTOR pathway.
Other drugs
Interferons
''General information:
Interferon.''
IFN-β suppresses the production of Th1 cytokines and the activation of monocytes. It is used to slow down the progression of
multiple sclerosis. IFN-γ is able to trigger lymphocytic
apoptosis.
Opioids
Prolonged use of
opioids may cause immunosuppression of both innate and adaptive immunity. Decrease in proliferation as well as immune function has been observed in macrophages as well as lymphocytes. It is thought that these effects are mediated by opioid receptors expressed on the surface of these immune cells.
Reference: Neurochem Res. 1996 Nov;21(11):1375-86.
TNF binding proteins
A
TNF-α (tumor necrosis factor alpha) binding protein is a monoclonal antibody or a circulating
receptor such as
infliximab (Remicade®),
etanercept (Enbrel®), or
adalimumab (Humira®) that binds to
TNF-α and prevent it from inducing the synthesis of IL-1 and IL-6 and the adhesion of lymphocyte activating molecules. They are used in the treatment of
rheumatoid arthritis,
ankylosing spondylitis,
Crohn's disease and
psoriasis.
TNF or the effects of TNF are also suppressed by various natural compounds, including
curcumin (an ingredient in
turmeric) and catechins (in
green tea).
These drugs may raise the risk of contracting
tuberculosis or inducing a latent infection to become active. Infliximab and adalimumab have label warnings stating that patients should be evaluated for latent TB infection and treatment should be initiated prior to starting therapy with them.
Mycophenolate
Mycophenolic acid acts as a non-competitive, selective and reversible inhibitor of
inosine monophosphate dehydrogenase (IMPDH), which is a key enzyme in the ''de novo''
guanosine nucleotide synthesis. In contrast to other human cell types, lymphocytes B and T are very dependent on this process.
Small biological agents
FTY720 is a new synthetic immunosuppressant, currently in phase 3 of clinical trials. It increases the expression or changes the function of certain adhesion molecules (α4/β7
integrin) in lymphocytes, so they accumulate in the
lymphatic tissue (lymphatic nodes) and their number in the circulation is diminished. In this respect, it differs from all other known immunosuppressants.
External links
★
Pancreas-Kidney Transplantation: Drugs, a brief history of immunosuppressive drugs. Accessed on 21 August 2005.
★
WSAVA 2001 - Immunosuppressive drug therapy, from the veterinary point of view. By Mark Papich. Accessed on 21 August 2005.
★
Newer Immunosuppressive Drugs;A Review -Gummert et al. - J Am Soc Nephrol 10:1366-1380, 1999. Free full text at
JASN. Accessed on 21 August 2005.
★
Principles and Practice of Monitoring Immunosuppressive Drugs. W.V.Armstrong, J Lab Med, 2002, 26 (1/2): 27-36. PDF. Accessed on 21 August 2005.
★
Are Immunosuppressive Drugs a Useful Adjuvant to Treatment of HIV with Antiretrovirals?. Hivandhepatitis.com. Accessed on 21 August 2005.
★
Immunosuppression. By Randy P Prescilla, MD; accessed on Emedicine.com on 21 August 2005
★
National Kidney Foundation: A to Z Health Guide, answers to some frequently asked questions about immunosuppression in renal transplatation for a layman. Accessed on 21 August 2005.
★
Immunosuppressants, Pharmacologic profile. Drugguide.com. Accessed on 21 August 2005.
★
Immunosuppressants, a collection of links at
About.com. Accessed ob 21 August 2005.
★
العربية
中国
Français
Deutsch
Ελληνική
हिन्दी
Italiano
日本語
Português
Русский
Español
![Last Minute Travel Deals: Make Sure You\](images/articles/thumbs/klastminutethumb.jpg "Last Minute Travel Deals: Make Sure You\")
![Walking in Waikiki: The Sauce-erer\](images/articles/thumbs/waikikidrinkumbrellathumb.jpg "Walking in Waikiki: The Sauce-erer\")
