Antibodies in the Kidd blood group system show a great deal of serolog
ical variability, are notoriously elusive and hence evoke difficulties
in detection. However, they have been regularly reported as causing s
evere immediate or delayed haemolytic transfusion reactions and this c
linical potential has been largely attributed to their complement bind
ing ability. In initial investigations on 43 anti-Jk(a)/Jk(b) sera wit
h a range of titres of IgG antibody only a few seemed to fix complemen
t, though following repeated tests on 20 of these sera a further five
were shown to bind complement, making a total of 12 (27.9%) showing ev
idence of complement binding. Twenty-three sera were unavailable for r
e-testing. Subsequent tests revealed that only those sera which showed
direct agglutination or were positive with an anti-IgM reagent in an
indirect antiglobulin test (IAT) fixed complement. Evaluations on the
IgG fractions of six selected potent anti-Jk(a) sera failed to reveal
any complement-fixing ability although all the original sera bound com
plement avidly and contained variable amounts of IgM antibody, some at
very low subagglutinating levels. These findings challenge past perce
ptions and give cause for reflection on the changing methodologies and
strategies which could unduly compromise the detection of these poten
tially clinically damaging antibodies.