Similarly, Mahesula et al. [57], using quantitative tandem mass spectrometry-based proteomics at numerous time points, reported a correlation of expression levels of CD47 and other related proteins with importance in the disease progression in the EAE animal model of MS, including MBP:223-228, which corresponded to the basic myelin protein, and MIF:79-87, which corresponded to a pro-inflammatory cytokine that suppresses migration of macrophages [57]. The gene discussed is CD47; the disease is myeloid sarcoma.