C-reactive protein (CRP) was discovered by Tillett and Francis’ in the sera of patients with various infectious and inflammatory diseases as a material which precipitated pneumococcal C-polysaccharide (CPS). Subsequently Abernethy and Ave $ characterized CRP as a protein and identified the requirement for calcium ions in its interaction with CPS, while they and established that the appearance of CRP in the serum is a nonspecific response to infection, inflammation and tissue damage. Abernethy and Averf also introduced the term “acute phase sera” to designate samples obtained from patients in the acute phase of infectious diseases. CRP was called the “acute phase protein” and this term was subsequently applied to the large number of other plasma proteins, the concentrations of which are raised in acute phase sera. At an early stage Abernethy’reported the presence of a precipitin comparable to CRP in acute phase monkey serum and, although he had been unable to find any in mouse or rabbit sera, Anderson and McCarty’later described the existence