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P Pierson

Publications and source records attributed to P Pierson.

7 recordsLinked to original sources

The effect of colchicine-specific active immunization on colchicine toxicity and disposition in the rabbit.

Anti-colchicine antibodies raised in rabbits are effective at protecting rabbits from acute colchicine intoxication. The positive effect depends on the ratio between the binding site capacity of the specific antibodies and the colchicine dose. Immunized rabbits receiving 6 mg/kg colchicine intravenously (LD100) died within 8 h as rapidly as those of the non-immunized control group. In contrast, if the colchicine dose was reduced to 3 mg/kg (LD83), rabbits were protected and mortality decreased to 17%. Study of plasma colchicine pharmacokinetics indicated that colchicine was totally sequestrated by antibodies in the 3 mg/kg group and only 55-80% sequestrated in 6 mg/kg group. This sequestration contributed to reducing colchicine diffusion into tissues (the volume of distribution decreased 7-fold) and to increasing the terminal half-life and the total body clearance of the drug. Moreover, as the slope of the dose-lethality curve was steep, a small binding capacity was sufficient to neutralize colchicine toxicity at 3 mg/kg. Results clearly indicate that anti-colchicine antibodies are able to effectively sequestrate colchicine. Moreover, the amount of circulating antibodies is a crucial limiting factor for the effectiveness of immunotoxicotherapy.

Animals

Immunotoxicotherapy: present status and future trends.

Immunotoxicotherapy (ITT) is currently used in humans for the treatment of snake venom and cardiac glycoside poisoning. Other toxins have been studied in animals or in vitro to assess their suitability as candidates for detoxification by specific antibodies. Testing conditions are often empirical suggesting that numerous improvements need to be introduced in ITT. Basic mechanisms in ITT include three phases: sequestration, extraction and elimination. The pharmacokinetics of these three phases depend on the type of antidotal binding site (ABS). IgG or its Fab2, Fab or Fv fragment are the possible choices. The Fab fragment is the most frequently used ABS because of its diffusion properties in the peripheral compartments and its renal excretion by glomerular filtration. Toxicokinetic and pharmacokinetic considerations indicate that the dosage cannot be satisfactorily calculated from stoichiometric principles. Study of the toxin dose-lethality curves shows that ABS dosage can be lowered. Moreover, clinical data reveal that some FAb fragments are directly eliminated without acting on toxin molecules. In order to counteract these drawbacks, a compromise between dosage and duration of infusion is suggested. Other improvements will stem from advances in immunologic methodology. Monoclonal and chimeric antibodies are new tools that will help resolve the clinical problems of immunogenicity and adverse reactions associated with polyclonal ABS.

Animals

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