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Mycophenolate

Manufactured by Genentech

Mycophenolate is a lab equipment product used for immunosuppression. It is a chemical compound that inhibits the enzyme inosine monophosphate dehydrogenase, which is essential for the de novo synthesis of guanine nucleotides. This mechanism of action leads to the inhibition of lymphocyte proliferation.

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3 protocols using mycophenolate

1

Xenogeneic Lung Transplant Immunosuppression

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To minimize the risk of rejection, an immunosuppression regimen informed by current practices in clinical transplantation, and described for use in xeno-support of human lungs, was used (Figure 1B).14 ,15 (link) At 4 hours before cross-circulation, xeno-support swine were anesthetized, intubated, and administered cobra venom factor (1 mg; Sigma-Aldrich) to deplete complement activity.16 (link) Intravenous diphenhydramine (50 mg; West Ward) and methylprednisolone (1 g; Pfizer) were administered to limit the inflammatory response associated with cobra venom factor. Intravenous tacrolimus (5 mg; Astellas) and mycophenolate (500 mg; Genentech) were also administered before reperfusion and redosed every 12 hours (Supplemental Figure S1C, http://links.lww.com/HEP/F706). methylprednisolone (125 mg; Pfizer) was readministered every 8 hours after the initial dosage.
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2

Immunosuppressive Regimen for Xenotransplantation

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To minimize the risk of rejection, an immunosuppression regimen informed by current practices in clinical transplantation, and previously described for use in xeno-support of human lungs, was used (Fig. 1b).14 ,15 (link) At 4 h before cross-circulation, xeno-support swine were anesthetized, intubated and administered cobra venom factor (CVF, 1 mg; Sigma-Aldrich) to deplete complement activity.16 Intravenous diphenhydramine (50 mg; West-Ward) and methylprednisolone (1 g; Pfizer) were administered to limit the inflammatory response associated with CVF. Intravenous tacrolimus (5 mg; Astellas) and mycophenolate (500 mg; Genentech) were also administered prior to reperfusion and re-dosed every 12 hours (Fig. S1c). methylprednisolone (125 mg; Pfizer) was re-administered every 8 hours after the initial dose.
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3

Xenogeneic Lung Transplant Immunosuppression

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To minimize the risk of immunologic rejection, an immunosuppression regimen informed by established protocols and current practices in clinical lung transplantation was used (Fig. 1B). Four hours before initiation of xenogeneic XC, xeno-support swine were anesthetized, intubated, and administered CVF (1 mg; Sigma-Aldrich) to deplete complement activity (61 (link), 62 (link)). Intravenous diphenhydramine (50 mg; West-Ward Pharmaceuticals) and methylprednisolone (1 g; Pfizer) were administered to mitigate hemodynamic instability occasionally associated with CVF. Intravenous tacrolimus (5 mg; Astellas) and mycophenolate (500 mg; Genentech) were also administered before reperfusion and redosed every 12 hours. methylprednisolone (125 mg; Pfizer) was readministered every 8 hours after the initial dose.
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