Journal of Antimicrobial Chemotherapy, Vol 40, 475-483, Copyright © 1997 by The British Society for Antimicrobial Chemotherapy
WN Hustinx, K Kraaijeveld, AI Hoepelman and J Verhoef
The ability of antibodies against the core glycolipid (CGL) of endotoxin to
protect experimentally infected animals against death from Gram-negative
sepsis is reviewed. The limitations and confounding factors inherent to
animal models of sepsis are also briefly discussed. This review considers
30 studies in mice and 12 in other animal species that investigated
protection against heterologous challenge by passive immunization with
anti-CGL antibodies. In 28 (67%) of the reviewed studies antibodies were
found to be protective, either prophylactically (n = 17) or therapeutically
(n = 11). With the possible exception of the type of antibody preparation
that was used (monoclonal versus polyclonal antibodies), none of the many
differences in the experimental protocols were clearly correlated with
success. Convincing proof is still lacking for any of the hypothetical
mechanisms of protection by anti-CGL antibodies. Moreover, the evidence
that protection by these antibodies is attributable to their anti-CGL
specificity is poor. The available data raise serious questions about the
validity of the concept underlying the search for broadly cross- protective
antibodies raised against the core region of endotoxin. However, continuing
research suggests that endotoxin still is a valid target in devising new
adjunctive treatment strategies to improve the outcome of serious
Gram-negative infections.
REVIEWS
Cross-protection by anti-core glycolipid antibodies: evidence from animal experiments
Eijkman-Winkler Institute for Medical & Clinical Microbiology, Utrecht University Hospital, The Netherlands.
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