At present, it is difficult to distinguish between bacterial infections and
sterile inflammatory processes using radiopharmaceuticals. This is so for
a variety of reasons, including binding to bacteria with low affinity (e.g.
infection) and binding to a specific micro-organism (e.g. radiolabelled mo
noclonal antibodies or F(ab)(2) fragments thereof against micro-organisms).
In this review we propose that radiolabelled antimicrobial peptides should
be the first choice in the development of new radiopharmaceuticals for ima
ging of bacterial infections. Antimicrobial peptides are a recently discove
red component of the innate defence system of plants, animals and humans. T
hese peptides, which now number more than 100, with proven microbicidal act
ivity against a variety of micro-organisms, share certain properties, such
as their small size and cationic charge. The latter allows them to bind pre
ferentially to a broad spectrum of micro organisms. We have recently demons
trated that radiolabelled human defensins allow the rapid visualization of
bacterial infections in mice. Furthermore, binding of this antimicrobial pe
ptide to bacteria is the major factor contributing to the accumulation of t
his tracer in bacterial infections. Based on these considerations, we belie
ve that radiolabelled antimicrobial peptides will be an important asset in
the imaging of infections in patients. ((C) 1998 Lippincott Williams & Wilk
ins).