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Successful vaccination of sheep against footrot and attempts to eradicate the disease depend on there being a limit to the antigenic diversity of the causative bacterium, Bacteroides nodosus. Fimbrial antigenic variation was therefore investigated in vivo, both under conditions of chronic infection and under the pressure of a vaccine-induced immune response, to ascertain whether this represented an obstacle to such goals. Material was available from 5 experiments and although B. nodosus appeared to have undergone changes in its fimbrial antigens in one of these, the possibility that superinfection was responsible for the variation detected could not be ruled out because all sheep in this case were maintained at pasture. Overall, the results provided no evidence of fimbrial antigenic shift in B. nodosus in vivo and in conclusion, the survival of the organism in the sheep's foot, both in long-term natural infection and following vaccination, must therefore be related to factors other than the ability to undergo antigenic variation in order to evade the host's immune response. 相似文献
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D. A. Hedges B.Sc.Agr. T. F. Reardon M.Sc.Agr. C.S.I.R.O. 《Australian veterinary journal》1975,51(2):88-90
Data are presented on the effects of the use of pregnant mare serum gonadotrophin (PMS) and of increased liverweight on the number of lambs born, or in utero, in mature fine-woolled Merino ewes. The primary effect of increased bodyweight was to reduce the number of barren ewes whereas the main effect of PMS treatment was to increase the level of twinning among those ewes which conceived. The 2 effects appeared to be additive but it is pointed out that the survival rate of the lambs will be an important consideration in assessing the relative merits of the 2 treatments. 相似文献
106.
Lo JC Wang Y Tumanov AV Bamji M Yao Z Reardon CA Getz GS Fu YX 《Science (New York, N.Y.)》2007,316(5822):285-288
Hyperlipidemia, one of the most important risk factors for coronary heart disease, is often associated with inflammation. We identified lymphotoxin (LT) and LIGHT, tumor necrosis factor cytokine family members that are primarily expressed on lymphocytes, as critical regulators of key enzymes that control lipid metabolism. Dysregulation of LIGHT expression on T cells resulted in hypertriglyceridemia and hypercholesterolemia. In low-density lipoprotein receptor-deficient mice, which lack the ability to control lipid levels in the blood, inhibition of LT and LIGHT signaling with a soluble lymphotoxin beta receptor decoy protein attenuated the dyslipidemia. These results suggest that the immune system directly influences lipid metabolism and that LT modulating agents may represent a novel therapeutic route for the treatment of dyslipidemia. 相似文献
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