“…Hemolysis in chronic cold agglutinin disease is usually caused by idiotypically homogeneous IgM kappa-type autoantibodies with specificity for the I antigen [21]. However, the agglutinins may display heterogenity in regards to the light-chain type [5,7], heavy-chain isotype [1,2,6,8,19,20,27] and antibody specificity [5,6]. Cold agglutinins produced as a response to Mycoplasma pneu moniae infections are usually polyclonal IgM anti-I anti bodies [22], whereas IgG anti-i (sometimes in combina tion with IgM rheumatoid factor) are seen in infectious mononucleosis [9,10], and IgG anti-P autoantibodies are characteristic of paroxysmal cold hemoglobinuria [11,25].…”