Infections associated with immunosuppressants: Difference between revisions

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m (Text replacement - "[[Human herpesviruses" to "[[Herpesviridae")
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|CD52
|CD52
|depletes T and B cells
|depletes T and B cells
|[[Human herpesviruses|herpesviruses]], especially [[CMV]] and [[EBV]], [[BK virus]], [[PML]], [[Pneumocystis]], [[Cryptococcus]], [[dimorphic fungi]]
|[[Herpesviridae|herpesviruses]], especially [[CMV]] and [[EBV]], [[BK virus]], [[PML]], [[Pneumocystis]], [[Cryptococcus]], [[dimorphic fungi]]
|-
|-
|[[rituximab]]
|[[rituximab]]
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|CD3
|CD3
|depletes T cells
|depletes T cells
|[[Human herpesviruses|herpesviruses]], especially [[CMV]] and [[EBV]], [[BK virus]], [[Pneumocystis]], [[Cryptococcus]], [[dimorphic fungi]]
|[[Herpesviridae|herpesviruses]], especially [[CMV]] and [[EBV]], [[BK virus]], [[Pneumocystis]], [[Cryptococcus]], [[dimorphic fungi]]
|-
|-
|corticosteroids
|corticosteroids
|multiple
|multiple
|multiple
|multiple
|[[LTBI]] reactivation, [[Human herpesviruses|herpesviruses]] (especially [[HSV]]/[[VZV]]), [[Candida]], [[Pneumocystis]], [[dimorphic fungi]], [[invasive fungal infection]]
|[[LTBI]] reactivation, [[Herpesviridae|herpesviruses]] (especially [[HSV]]/[[VZV]]), [[Candida]], [[Pneumocystis]], [[dimorphic fungi]], [[invasive fungal infection]]
|-
|-
|[[adalimumab]]
|[[adalimumab]]

Revision as of 17:39, 18 September 2020

Drug Target Effect Infections
alemtuzumab CD52 depletes T and B cells herpesviruses, especially CMV and EBV, BK virus, PML, Pneumocystis, Cryptococcus, dimorphic fungi
rituximab CD20 depletes B cells HBV reactivation, PML, Pneumocystis
antithymocyte globulin CD3 depletes T cells herpesviruses, especially CMV and EBV, BK virus, Pneumocystis, Cryptococcus, dimorphic fungi
corticosteroids multiple multiple LTBI reactivation, herpesviruses (especially HSV/VZV), Candida, Pneumocystis, dimorphic fungi, invasive fungal infection
adalimumab TNF-α intracellular organisms, including tuberculosis, non-tuberculous mycobacteria, Aspergillus, dimorphic fungi, Pneumocystis, Cryptococcus, Candida, hepatitis B, human herpesviruses (especially HSV and VZV), Strongyloides stercoralis, Legionella, Nocardia, Salmonella, Staphylococcus aureus septic arthritis, Leishmania, Plasmodium, Babesia, Strongyloides
infliximab
golimumab
etanercept
anakinra IL-1 prevents cytokines from activating B and T cells LTBI reactivation
canakinumab
rilonacept
basiliximab CD-25 block IL-2 receptor, preventing activation of T, B, and NK cells human herpesviruses
daclizumab
tocilizumab IL-6 prevents cytokine production LTBI reactivation, Candida, Aspergillus, Pneumocystis, dimorphic fungi, human herpesviruses
abatacept CD28 blocks APCs from binding T cells EBV, PML, CMV, Pneumocystis, LTBI reactivation, hepatitis B reactivation, malignancies (lymphoma, lung cancer, and skin cancer)
belatacept
natalizumab integrin inhibits T cell migration
vedolizumab
eculizumab C5 inhibits terminal complement severe Neisseria meningitidis infections, Streptococcus pneumoniae, Haemophilus influenzae
ustekinumab IL-12 and IL-23 inhibits cytokines