Immunosuppressive therapy: Difference between revisions
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Before starting immunosuppressive therapy, consider the following investigations: |
Before starting immunosuppressive therapy, consider the following investigations: |
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* Tuberculin skin test |
* [[Tuberculin skin test]] |
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* Strongyloides serology, if from endemic country |
* [[Strongyloides]] serology, if from endemic country |
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* |
* [[Hepatitis B]] and [[Hepatitis C virus|C]] serology |
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* Cytomegalovirus serology |
* [[Cytomegalovirus]] serology |
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* HIV serology |
* [[HIV]] serology |
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== Management == |
== Management == |
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* Latent TB infection: start treatment at least 4 weeks prior to starting the biologic |
* [[Latent tuberculosis infection|Latent TB infection]]: start treatment at least 4 weeks prior to starting the biologic |
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== Specific Medications == |
== Specific Medications == |
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{| class="wikitable" |
{| class="wikitable sortable" |
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! Medications |
! Medications |
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! Target |
! Target |
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!Type |
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!Indications |
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! Specific Risks |
! Specific Risks |
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| [[Eculizumab]] |
| [[Eculizumab]] |
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| C5 complement |
| C5 complement |
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| Meningococcus (very high risk), needs MCV4 + MenB + pen prophylaxis |
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| [[meningococcus]] (very high risk; needs MCV4 + MenB + pen prophylaxis) |
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| [[Rituximab]] |
| [[Rituximab]] |
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| CD20 |
| CD20 |
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| Long-term B cell depletion |
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|specific risk of [[PML]] and [[HBV]]; serious bacterial infections, [[PML]], [[parvovirus]], [[CMV]], [[HSV]], and disseminated [[VZV]] infections, [[HBV]] and [[HCV]] reactivation |
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|[[Ocrelizumab]] |
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|CD20 |
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| [[Natalizumab]] |
| [[Natalizumab]] |
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| α4-integrin |
| α4-integrin |
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|humanized IgG4 |
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| JC virus |
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| specific risk of [[PML]]; [[Herpesviridae|herpesvirus]] infections, [[influenza]], [[Cryptosporidium]] diarrhea, bacterial [[pneumonia]] and [[UTI]], [[Pneumocystis jirovecii|PCP]], [[Mycobacterium avium-intracellulare]] infection, [[Aspergillus]] and [[Burkholderia cepacia]] infections |
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| [[Ibrutinib]] |
| [[Ibrutinib]] |
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| Bruton's tyrosine kinase (BTK), on B cells |
| Bruton's tyrosine kinase (BTK), on B cells |
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| Invasive aspergillosis and other fungal infections |
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| Invasive [[aspergillosis]] and other [[Invasive fungal infection|fungal infections]] |
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|Steroids |
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|[[Cyclosphosphamide]] |
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|Antimetabolite |
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|[[Leflunomide]] |
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|Antimetabolite |
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|[[Methotrexate]] |
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|Antimetabolite |
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|[[Azathioprine]] |
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|Antimetabolite |
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|[[6-mercaptopurine]] |
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|Antimetabolite |
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|[[Mycophenolic acid]] |
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|Antimetabolite |
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|[[Mycophenolate mofetil]] |
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|Antimetabolite |
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|[[Tacrolimus]] |
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|Calcineurin inhibitor |
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|[[Cyclosporine]] |
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|Calcineurin inhibitor |
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|[[Sirolimus]] |
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|Calcineurin inhibitor |
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|[[Baricitinib]] |
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|JAK inhibitor |
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|[[Tofacitinib]] |
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|JAK inhibitor |
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|[[Upadacitinib]] |
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|JAK inhibitor |
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|[[Adalimumab]] |
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|TNF-α |
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|human IgG1 |
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|serious pulmonary bacterial infections, [[TB]], [[candidiasis]], [[CMV]] infection, [[toxoplasmosis]], and [[nocardiosis]] |
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|[[Certolizumab pegol]] |
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|TNF-α |
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|humanized Fab' fragment |
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|serious pulmonary bacterial infections, [[TB]], viral and fungal infections |
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|[[Golimumab]] |
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|TNF-α |
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|[[Certolizumab pegol]] |
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|TNF-α |
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|[[Etanercept]] |
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|TNF-α |
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|human dimeric fusion protein |
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|serious bacterial infections, [[TB]], [[NTM]], [[listeriosis]], [[histoplasmosis]], [[candidiasis]], [[aspergillosis]], [[cryptococcosis]], [[nocardiasis]], [[Protozoa|protozoal]] and [[VZV]] infection |
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|[[Infliximab]] |
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|TNF-α |
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|chimeric IgG1 |
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|[[pneumonia]], [[sepsis]], [[TB]], [[NTM]], [[listeriosis]], [[histoplasmosis]], [[candidiasis]], [[aspergillosis]], [[cryptococcosis]], [[salmonellosis]], [[toxoplasmosis]], [[brucellosis]], [[bartonellosis]], [[leishmaniasis]], [[coccidiomycoses]], [[leprosy]], [[CMV]] infection, [[HBV]] reactivation |
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|[[Sulfasalazine]] |
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|Anti-inflammatory |
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|[[5-aminosalicylic acid]] and [[mesalamine]] |
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|Anti-inflammatory |
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|[[Anakinra]] |
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|IL-1 |
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|non-glycosylated IL-1 receptor |
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|[[pneumonia]], [[cellulitis]], [[TB]], unspecified [[Mycobacteria|mycobacterial]] and fungal infections |
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|[[Rilonacept]] |
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|IL-1 |
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|dimeric fusion protein IL-1 inhibitor |
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|[[meningitis]], [[NTM]], severe [[bronchitis]] |
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|[[Canakinumab]] |
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|IL-1 |
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|[[Tocilizumab]] |
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|Anti-IL6 |
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|[[Sarilumab]] |
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|Anti-IL6 |
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|[[Ustekinumab]] |
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|Anti-IL12/IL23 |
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|[[Secukinumab]] |
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|Anti-IL17 |
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|human IgG1κ monoclonal antibody |
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|[[psoriasis]], [[ankylosing spondylitis]], and [[psoriatic arthritis]] |
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|[[Ixekizumab]] |
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|Anti-IL17 |
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|[[Brodalumab]] |
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|Anti-IL17 receptor |
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|[[Belimumab]] |
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|Anti-BLyS |
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|[[Guselkumab]] |
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|Anti-IL23 |
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|[[Risankizumab]] |
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|Anti-IL23 |
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|[[Abatacept]] |
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|T-cell costimulation inhibitor |
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|fusion protein |
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|[[pneumonia]], [[sepsis]], [[aspergillosis]], [[sinusitis]], [[candidiasis]], [[bronchitis]], [[skin and soft tissue infection]], viral infections with [[HSV]] and [[VZV]] |
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|[[Fingolimod]] |
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|Selective T-cell costimulation blocker |
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|[[Siponimod]] |
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|S1PR agonist |
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|[[Ozanimod]] |
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|S1PR agonist |
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|[[Apremilast]] |
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|Phosphodiesterase inhibitor |
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|[[Vedolizumab]] |
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|Anti-integrin |
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|[[Efalizumab]] |
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|CD11a |
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|humanized IgG1 |
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|generally mild; [[pneumonia]], [[cellulitis]], [[abscess]], [[sepsis]], [[Legionella]] pneumonia, [[necrotizing fasciitis]], [[TB]], [[PML]] |
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|[[Alefacept]] |
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|T-cell activation |
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|fusion protein |
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|[[cellulitis]], [[abscess]], wound infections, [[Toxic shock syndrome|toxic shock]], [[pneumonia]], [[appendicitis]], [[cholecystitis]], [[gastroenteritis]], [[NTM]] infection, [[influenza virus]], [[HCV]], and [[Herpesviridae|herpesvirus]] infections |
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|[[Alemtuzumab]] |
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|CD52 |
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|humanized IgG1 |
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|causes prolonged [[lymphopenia]]; overwhelming [[bacteremia]], pneumonia, [[meningitis]], [[CMV]], [[VZV]], and [[HSV]] infections, [[PCP]], [[PML]], [[adenovirus]] infection, [[acanthamebiasis]], [[toxoplasmosis]], [[histoplasmosis]], [[cryptococcosis]], [[aspergillosis]], [[Fusarium]] infection, [[Scedosporium]] infection, [[BK virus]] infection, [[HHV-6]] infection, [[candidiasis]], [[parvovirus]] infection, [[mucormycosis]], [[TB]], [[Balamuthia mandrillaris]] infection, [[NTM]] infection, [[BCG]]-related infection, [[Rhodococcus]] infection, [[HBV]] reactivation |
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|[[90Y-ibritumomab tiuxetan|<sup>90</sup>Y-ibritumomab tiuxetan]] |
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|CD20 |
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|radioconjugated murine IgG1 |
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|[[pneumonia]], [[sepsis]], [[cellulitis]], [[colitis]], [[diarrhea]], [[empyema]], [[osteomyelitis]], [[pericarditis]], viral [[pneumonia]] and [[viral hepatitis]] |
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|[[131I-tositumomab|<sup>131</sup>I-tositumomab]] |
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|CD20 |
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|radioconjugated murine IgG2 |
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|[[pneumonia]], septicemia, [[bronchitis]], skin infections, viral infections |
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|[[Gemtuzumab ozogamicin]] |
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|CD33 |
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|humanized IgG4 conjugated to calichaemicin |
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|causes prolonged [[neutropenia]]; [[sepsis]], [[pneumonia]], [[HSV]] infection, usual opportunistic infections with [[neutropenia]], unusual pathogens include [[Staphylococcus hominis]], [[Agrobacterium radiobacter]], [[Acinetobacter lwoffii]], [[Rhodococcus]], and [[Pantoea agglomerans]] |
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|[[Bevacizumab]] |
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|VEGF |
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|humanized IgG1 |
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|severe [[neutropenia]]; sepsis, anaerobic [[liver abscess]] with [[Bacteroides fragilis]], [[Fusarium]] nasal septal infection, [[endophthalmitis]], intraocular injection including [[Bacillus cereus]] and [[coagulase-negative Staphylococcus]] |
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|[[Cetuximab]] |
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|ErbB1 |
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|chimeric human-murine IgG1 |
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|[[paronychia]] caused by [[Staphylococcus aureus]], [[abscess]], [[sepsis]] |
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|[[Panitumumab]] |
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|ErbB1 |
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|human IgG2 |
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|[[paronychia]], [[abscess]], [[sepsis]] |
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|[[Trastuzumab]] |
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|HER2 |
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|human IgG1 |
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|[[febrile neutropenia]] |
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|[[Basiliximab]] |
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|CD25 |
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|chimeric human-murine IgG1 |
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|bacterial, [[CMV]], and [[HSV]] infections, [[aspergillosis]], [[nocardiosis]], [[candidiasis]], and [[Protozoa|protozoal infections]] |
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|[[Daclizumab]] |
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|CD25 |
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|humanized IgG1 |
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|[[nocardiosis]], [[legionellosis]], [[Non-tuberculous mycobacteria|MOTT infection]], [[TB]], viral infection with [[CMV]], [[BK virus]], [[adenovirus]], [[HSV]], [[RSV]], or [[influenza virus]], fungal infections with [[Aspergillus]], [[Scedosporium]], [[Cunninghamella]], and [[Candida]] |
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|[[Muromonab]] |
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|CD3 |
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|murine IgG2 |
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|bacterial infections, including [[Listeria]], [[Nocardia]], and [[Non-tuberculous mycobacteria|MOTT]] infections; infections with [[Aspergillus]], [[Candida]], [[Cryptococcus]], or [[dermatophytes]]; PCP; infections with [[Toxoplasma gondii]], [[CMV]], [[EBV]], [[HSV]], [[Viral hepatitis|hepatitis viruses]], [[VZV]], [[adenovirus]], [[enterovirus]], [[RSV]], and parainfluenza virus |
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|[[Abciximab]] |
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|GPIIb/IIIa |
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|Fab' fragment of chimeric human-murine IgG1 |
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|[[pneumonia]] |
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|[[Omalizumab]] |
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|IgE |
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|humanized IgG1 |
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|none |
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|[[Palivizumab]] |
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|F protein of [[RSV]] |
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|humanized IgG1 |
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|[[otitis media]] |
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== Further Reading == |
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* Infectious complications associated with monoclonal antibodies and related small molecules. ''Clin Microbiol Rev''. 2009 Apr;22(2):274-90. doi: [https://doi.org/10.1128/CMR.00040-08 10.1128/CMR.00040-08] |
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[[Category:Immunocompromised hosts]] |
[[Category:Immunocompromised hosts]] |
Latest revision as of 18:19, 6 June 2023
Screening
Before starting immunosuppressive therapy, consider the following investigations:
- Tuberculin skin test
- Strongyloides serology, if from endemic country
- Hepatitis B and C serology
- Cytomegalovirus serology
- HIV serology
Management
- Latent TB infection: start treatment at least 4 weeks prior to starting the biologic
Specific Medications
Medications | Target | Type | Indications | Specific Risks |
---|---|---|---|---|
Eculizumab | C5 complement | meningococcus (very high risk; needs MCV4 + MenB + pen prophylaxis) | ||
Rituximab | CD20 | specific risk of PML and HBV; serious bacterial infections, PML, parvovirus, CMV, HSV, and disseminated VZV infections, HBV and HCV reactivation | ||
Ocrelizumab | CD20 | |||
Natalizumab | α4-integrin | humanized IgG4 | specific risk of PML; herpesvirus infections, influenza, Cryptosporidium diarrhea, bacterial pneumonia and UTI, PCP, Mycobacterium avium-intracellulare infection, Aspergillus and Burkholderia cepacia infections | |
Ibrutinib | Bruton's tyrosine kinase (BTK), on B cells | Invasive aspergillosis and other fungal infections | ||
Steroids | ||||
Cyclosphosphamide | Antimetabolite | |||
Leflunomide | Antimetabolite | |||
Methotrexate | Antimetabolite | |||
Azathioprine | Antimetabolite | |||
6-mercaptopurine | Antimetabolite | |||
Mycophenolic acid | Antimetabolite | |||
Mycophenolate mofetil | Antimetabolite | |||
Tacrolimus | Calcineurin inhibitor | |||
Cyclosporine | Calcineurin inhibitor | |||
Sirolimus | Calcineurin inhibitor | |||
Baricitinib | JAK inhibitor | |||
Tofacitinib | JAK inhibitor | |||
Upadacitinib | JAK inhibitor | |||
Adalimumab | TNF-α | human IgG1 | serious pulmonary bacterial infections, TB, candidiasis, CMV infection, toxoplasmosis, and nocardiosis | |
Certolizumab pegol | TNF-α | humanized Fab' fragment | serious pulmonary bacterial infections, TB, viral and fungal infections | |
Golimumab | TNF-α | |||
Certolizumab pegol | TNF-α | |||
Etanercept | TNF-α | human dimeric fusion protein | serious bacterial infections, TB, NTM, listeriosis, histoplasmosis, candidiasis, aspergillosis, cryptococcosis, nocardiasis, protozoal and VZV infection | |
Infliximab | TNF-α | chimeric IgG1 | pneumonia, sepsis, TB, NTM, listeriosis, histoplasmosis, candidiasis, aspergillosis, cryptococcosis, salmonellosis, toxoplasmosis, brucellosis, bartonellosis, leishmaniasis, coccidiomycoses, leprosy, CMV infection, HBV reactivation | |
Sulfasalazine | Anti-inflammatory | |||
5-aminosalicylic acid and mesalamine | Anti-inflammatory | |||
Anakinra | IL-1 | non-glycosylated IL-1 receptor | pneumonia, cellulitis, TB, unspecified mycobacterial and fungal infections | |
Rilonacept | IL-1 | dimeric fusion protein IL-1 inhibitor | meningitis, NTM, severe bronchitis | |
Canakinumab | IL-1 | |||
Tocilizumab | Anti-IL6 | |||
Sarilumab | Anti-IL6 | |||
Ustekinumab | Anti-IL12/IL23 | |||
Secukinumab | Anti-IL17 | human IgG1κ monoclonal antibody | psoriasis, ankylosing spondylitis, and psoriatic arthritis | |
Ixekizumab | Anti-IL17 | |||
Brodalumab | Anti-IL17 receptor | |||
Belimumab | Anti-BLyS | |||
Guselkumab | Anti-IL23 | |||
Risankizumab | Anti-IL23 | |||
Abatacept | T-cell costimulation inhibitor | fusion protein | pneumonia, sepsis, aspergillosis, sinusitis, candidiasis, bronchitis, skin and soft tissue infection, viral infections with HSV and VZV | |
Fingolimod | Selective T-cell costimulation blocker | |||
Siponimod | S1PR agonist | |||
Ozanimod | S1PR agonist | |||
Apremilast | Phosphodiesterase inhibitor | |||
Vedolizumab | Anti-integrin | |||
Efalizumab | CD11a | humanized IgG1 | generally mild; pneumonia, cellulitis, abscess, sepsis, Legionella pneumonia, necrotizing fasciitis, TB, PML | |
Alefacept | T-cell activation | fusion protein | cellulitis, abscess, wound infections, toxic shock, pneumonia, appendicitis, cholecystitis, gastroenteritis, NTM infection, influenza virus, HCV, and herpesvirus infections | |
Alemtuzumab | CD52 | humanized IgG1 | causes prolonged lymphopenia; overwhelming bacteremia, pneumonia, meningitis, CMV, VZV, and HSV infections, PCP, PML, adenovirus infection, acanthamebiasis, toxoplasmosis, histoplasmosis, cryptococcosis, aspergillosis, Fusarium infection, Scedosporium infection, BK virus infection, HHV-6 infection, candidiasis, parvovirus infection, mucormycosis, TB, Balamuthia mandrillaris infection, NTM infection, BCG-related infection, Rhodococcus infection, HBV reactivation | |
90Y-ibritumomab tiuxetan | CD20 | radioconjugated murine IgG1 | pneumonia, sepsis, cellulitis, colitis, diarrhea, empyema, osteomyelitis, pericarditis, viral pneumonia and viral hepatitis | |
131I-tositumomab | CD20 | radioconjugated murine IgG2 | pneumonia, septicemia, bronchitis, skin infections, viral infections | |
Gemtuzumab ozogamicin | CD33 | humanized IgG4 conjugated to calichaemicin | causes prolonged neutropenia; sepsis, pneumonia, HSV infection, usual opportunistic infections with neutropenia, unusual pathogens include Staphylococcus hominis, Agrobacterium radiobacter, Acinetobacter lwoffii, Rhodococcus, and Pantoea agglomerans | |
Bevacizumab | VEGF | humanized IgG1 | severe neutropenia; sepsis, anaerobic liver abscess with Bacteroides fragilis, Fusarium nasal septal infection, endophthalmitis, intraocular injection including Bacillus cereus and coagulase-negative Staphylococcus | |
Cetuximab | ErbB1 | chimeric human-murine IgG1 | paronychia caused by Staphylococcus aureus, abscess, sepsis | |
Panitumumab | ErbB1 | human IgG2 | paronychia, abscess, sepsis | |
Trastuzumab | HER2 | human IgG1 | febrile neutropenia | |
Basiliximab | CD25 | chimeric human-murine IgG1 | bacterial, CMV, and HSV infections, aspergillosis, nocardiosis, candidiasis, and protozoal infections | |
Daclizumab | CD25 | humanized IgG1 | nocardiosis, legionellosis, MOTT infection, TB, viral infection with CMV, BK virus, adenovirus, HSV, RSV, or influenza virus, fungal infections with Aspergillus, Scedosporium, Cunninghamella, and Candida | |
Muromonab | CD3 | murine IgG2 | bacterial infections, including Listeria, Nocardia, and MOTT infections; infections with Aspergillus, Candida, Cryptococcus, or dermatophytes; PCP; infections with Toxoplasma gondii, CMV, EBV, HSV, hepatitis viruses, VZV, adenovirus, enterovirus, RSV, and parainfluenza virus | |
Abciximab | GPIIb/IIIa | Fab' fragment of chimeric human-murine IgG1 | pneumonia | |
Omalizumab | IgE | humanized IgG1 | none | |
Palivizumab | F protein of RSV | humanized IgG1 | otitis media |
Further Reading
- Infectious complications associated with monoclonal antibodies and related small molecules. Clin Microbiol Rev. 2009 Apr;22(2):274-90. doi: 10.1128/CMR.00040-08