Abstract
Endotoxins from Gram-negative bacteria have been shown to be potent biological activators and are involved in many pathological reactions (Yagoda et al. 1990). Since endotoxins are ubiquitous compounds, they can create serious problems for the pharmaceutical industry. There are several examples of unavoidable drug contamination and of endotoxins that cannot be removed from recombinant procedures involving Escherichia coli bacteria (Yagoda et al. 1990). It is difficult to establish a true threshold dose at which endotoxins will cause clinical effects, but doses less than or equal to 3 ng/kg body weight (bw) can cause fever, chills and headache in humans (Elin et al. 1981). Another reference gives 5 endotoxin units (EU)/kg bw for similar clinical symptoms (Anon. 1987). Vaccines prepared using E. coli bacteria have a high potential for endotoxin content. This is important because endotoxin contamination in general can distort analyses of pharmacological studies and produce unpredictable and erratic effects on animals that receive contaminated vaccines. It is therefore important to identify possible effects of endotoxin-containing vaccines on various physiologic endpoints. It is also pertinent to assess the magnitude of any potential risks involved in using such vaccines. The purpose of this study was to evaluate the blood chemical and clinical response of castrated young boars to commercially available vaccines to E. coli where the bacteria have been formaldehyde killed and the endotoxins have not been removed.
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Acknowledgments
This study was supported by grants from the Swedish Council for Forestry and Agricultural Research.
References
- Anonymous: FDA's Guideline on Validation of the Limulus Amebocyte Lysate Test as an End-Product Endotoxin Test for Human and Animal Parenteral Drugs, Biological Products, and Medical Devices, 1987.
- N C. A clinical study on the effects of a Gram-negative bacterial endotoxin and cloprostenol in non-pregnant and 60 days pregnant gilts. Anim. Reprod. Sci. 1986;10:133–145. [Google Scholar]
- N C, H K. The effect of a bacterial endotoxin or cloprostenol on the clinical status and hormonal levels in 80-100 days pregnant gilts. Acta vet. scand. 1986;27:145–158. doi: 10.1186/BF03548160. [DOI] [PMC free article] [PubMed] [Google Scholar]
- N C, T K, S E. The effect of a Gram-negative bacterial endotoxin and cloprostenol on the plasma levels of 15-keto-13,14-dihy-dro-PGF2a, progesterone, oestradiol-17ß, oestrone sulphate and luteinizing hormone in non-pregnant and 60 days pregnant gilts. Anim. Reprod. Sci. 1986;10:147–162. [Google Scholar]
- H-G E, P R, P S. Die Bestimmung des Eisens mit der Guanidiniumchlorid/ Ferrozin-Methode. J. Clin. Chem. Clin. Biochem. 1979;77:149. [Google Scholar]
- RJ E, SM W, KPWJ M, L C, L A, C B, F O. Properties of reference Escherichia coli endotoxin and its phthal-ylated derivative in humans. J. inf. Dis. 1981;144:329–336. doi: 10.1093/infdis/144.4.329. [DOI] [PubMed] [Google Scholar]
- H H, L-E E, H K. Reduced response to intravenous endotoxin injections following repeated oral administration of endotoxin in the pig. Acta vet. scand. 1993;34:405–419. doi: 10.1186/BF03548185. [DOI] [PMC free article] [PubMed] [Google Scholar]
- E G, H K. Radioimmunoassay of the major plasma metabolite of PGF2a, 15-keto-13,14-dihydro-PGF2a. Methods Enzymol. 1982;86:320–339. doi: 10.1016/0076-6879(82)86204-6. [DOI] [PubMed] [Google Scholar]
- U M, H H, H K, Ä K. Effect of mimicking prepartum concentrations of estradiol-17ß on the inflammatory response to endotoxin in gilts. Am. J. Vet. Res. 1994;55:785–789. [PubMed] [Google Scholar]
- U M, H H. J. Vet. Med. B. 1998. Assaying granulocyte phagocytosis in vitro: effects of storage time and temperature of blood samples. [DOI] [PubMed] [Google Scholar]
- MM P, FL H, DJ M. Determination of copper and zinc in biological material. Clin. Chem. 1967;13:40–48. [PubMed] [Google Scholar]
- T, Kunavongkrit^A R. Chronical venous catheterization for frequent blood sampling in unrestrained pigs. Acta vet. scand. 1983;24:318–320. doi: 10.1186/BF03546736. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DL T, EF F. Determination of calcium in urine and serum by atomic absorption spectrophotometry (AAS). Clin. Chem. 1967;13:101–114. [PubMed] [Google Scholar]
- TJ V, MJ M, BP O ', VA L, H W, RL K, MP F. Bactericidal/permeability-increasing protein ameliorates acute lung injury in porcine endotoxemia. J. Appl. Physiol. 1994;76:2006–2014. doi: 10.1152/jappl.1994.76.5.2006. [DOI] [PubMed] [Google Scholar]
- CR Y, A-C B-F, N A, H K. Biological responses of sheep treated with en-dotoxin-contaminated superoxide dismutase and endotoxin preparations. Acta vet. scand. 1990;31:207–217. doi: 10.1186/BF03547563. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Österlundh I, Hoist TU, Magnusson U: Hormonal and immunological changes in the mammary gland of the sow at parturition. (Submitted for publication). [DOI] [PubMed]
