Major advances in our understanding of the immunobiology of complement were
made within the past 5 years primarily due to the development of gene-targ
eting technology. New strains of mice bearing specific deficiencies in seru
m complement proteins or their receptors were developed using this approach
. Characterization of these mice has provided new and exciting insights int
o the biology of the complement system. In this review, we discuss recent r
esults on two important aspects of the complement system, i) host protectio
n and inflammation, and ii) regulation of B lymphocytes of adaptive immunit
y. While these two roles appear distinct, they are linked. We discuss how n
atural antibody and classical pathway complement work together in host prot
ection against bacterial infection on the one hand bur, on the other, they
co-operate to induce inflammation as observed in reperfusion injury. Signif
icantly, the lymphocytes that produce natural antibody, the B-1 lymphocytes
, are regulated in part by the complement system.