Immunoneutralization of procalcitonin as therapy of sepsis

Author:

Becker K.L.1,Nylén E.S.2,Snider R.H.2,Müller B.3,White J.C.2

Affiliation:

1. George Washington University and Veterans Affairs Medical Center, Washington, DC, USA,

2. George Washington University and Veterans Affairs Medical Center, Washington, DC, USA

3. University of Basel, Switzerland

Abstract

Prior studies have demonstrated that the prohormone, procalcitonin (ProCT), and its component calcitonin precursors (CTpr) are increased in the serum of septic patients, correlate with the severity of the illness, and persist for relatively long periods of time. Animal studies in septic hamsters have revealed that the administration of ProCT is toxic and that immunoneutralization with IgG that is reactive to this molecule significantly improves survival. A large animal model of a very rapidly lethal polymicrobial sepsis has been developed in the pig in order to measure continuous physiological and metabolic parameters and also to compare the effects in this animal of an immunoneutralization, which is performed late in the course of the disease, to an identical, but early, therapy. Based upon the physiological and metabolic parameters, the late therapy, which was initiated during the fourth hour at a time when pigs were nearly moribund, was found to be as beneficial as early therapy. In both late and early therapy, the only animals to survive at the predetermined time of euthanasia were those which had received immunoneutralization therapy.

Publisher

SAGE Publications

Subject

Infectious Diseases,Cell Biology,Molecular Biology,Immunology,Microbiology

Reference28 articles.

1. Thyroid Hypocalcemic Principle and Recurrent Laryngeal Nerve Injury as Factors Affecting the Response to Parathyroidectomy in Rats1

2. CALCITONIN IN EXTRATHYROIDAL TISSUES OF MAN

3. Becker KL, Müller B., Nylén ES et al. Calcitonin gene family of peptides. Structure, molecular biology and effects. In: Bilizikian JP, Raisz LG, Rodin GA. (eds) Principles of Bone Biology, 2nd edn. San Diego, CA: Academic Press, 2002; 616—639.

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