“…More specifically, an impairment of the immune function of the spleen results in: (a) a reduction in IgM-memory B cells and a defective opsonization activity, thus predisposing to infections caused by encapsulated bacteria (mainly Streptococcus pneumoniae, Neisseria meningitidis and Haemophylus influenzae); and (b) a decrease in marginal zone B cells which, in turn, predisposes to the emergence of autoreactive T-cell clones, as a consequence of contemporary T-regulatory cell depletion, with the subsequent development of autoimmunity. Moreover, it must be remembered that the spleen also has an important filtering function; impairment results in (a) the defective removal of pits from erythrocytes, with a consequent increase in circulating pitted red cells and Howell-Jolly bodies, and (b) reduced platelet sequestration, leading to thrombocytosis, which, in turn, predisposes to thromboembolism [10,11].…”