${\lambda}_{M1}$ | Maximal rate at which M2 macrophages switch phenotype to become M1 macrophages | $6\times {10}^{-3}$ | day | [31] |

${\lambda}_{M2}$ | Maximal rate at which M1 macrophages switch phenotype to become M2 macrophages | $6\times {10}^{-3}$ | day | Est. from [31] |

${\lambda}_{MI4}$ | Production rate of M2 macrophages due to IL-4 | $1\times {10}^{-3}$ | day | [31] |

${\lambda}_{MI\gamma}$ | Production rate of M1 macrophages due to IFN-γ | $1\times {10}^{-3}$ | day | [31] |

${\lambda}_{MT\alpha}$ | Production rate of M1 macrophages due to TNF-α | $1\times {10}^{-3}$ | day | [31] |

${\lambda}_{T1M1}$ | Production rate of Th1 cells by M1 macrophages and IL-12 | 0.23 | day | [31] |

${\lambda}_{TI2}$ | Production rate of Th1 cells by IL-2 | 1 | day | [31] |

${\lambda}_{T2}$ | Production rate of Th2 cells | 0.8 | day | [31] |

${\lambda}_{I\gamma T1}$ | Production rate of IFN-γ by Th1 cells | $3.731\times {10}^{-3}$ | IU cell | [31] |

${\lambda}_{I12M1}$ | Production rate of IL-12 by M1 macrophages | 0.13 | IU cell | Est. from [31] |

${\lambda}_{I2T1}$ | Production rate of IL-2 by Th1 cells | 0.0672 | IU cell | [31] |

${\lambda}_{T\alpha M1}$ | Production rate of TNF-α by M1 macrophages | 13.91 | IU cell | [31] |

${\lambda}_{I1\beta M1}$ | Production rate of IL-1β by M1 macrophages | 0.1022 | IU cell | Est. from [31] |

${\lambda}_{I10M2}$ | Production rate of IL-10 by M2 macrophages | 0.02 | IU cell | [31] |

${\lambda}_{I4T2}$ | Production rate of IL-4 by Th2 cells | 0.0775 | IU cell | [31] |

${\lambda}_{I4M2}$ | Production rate of IL-4 by M2 macrophages | 0.3094 | IU cell | [31] |

${\lambda}_{I\alpha M2}$ | Production rate of IFN-alpha by M2 macrophages | $1\times {10}^{-5}$ | IU cell | [31] |

${\lambda}_{Treg}$ | Production rate of Tregs from Th0 cells due to TGF-β | 0.001 | day | Est. |

${\lambda}_{MI10}$ | Production rate of M2 macrophages due to IL-10 | $1\times {10}^{-3}$ | day | Est. from [31] |

${\lambda}_{I1\beta T1}$ | Production rate of IL-1beta by Th1 cells | 0.1022 | IU cell | Est. from [31] |