Enhanced immune response in bovine species
a bovine and immune-boosting technology, applied in the field of bovine immune activation in a member of the bovine species, can solve the problems of loss of milk production, negative impact on carcass characteristics, and current vaccination programs and pharmaceutical therapies are not optimal
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example 1
Evaluation of Cattle Receiving a DNA Immunomodulator Before or After Developing Natural Bovine Respiratory Disease
[0078]The purpose of this study was to determine the efficacy of the DNA immunomodulator administered to calves prior to and after developing natural cases of BRD.
Immunomodulator
[0079]The immunomodulator used in this study was a composition comprising a cationic lipid and non-coding DNA. The synthetic immunomodulator lipid components [1-[2-[9-(Z)-octadecenoyloxy]]-2-[8](Z)-heptadecenyl]-3-[hydroxyethyl]imidazolinium chloride (DOTIM) and a synthetic neutral lipid cholesterol were formulated to produce liposomes approximately 200 nm in diameter (See, U.S. Pat. No. 6,693,086). The DNA component was a 4242 base-pair non-coding DNA plasmid produced in E. coli, which, being negatively charged, associates with the positively-charged (cationic) liposomes (See, U.S. Pat. No. 6,693,086).
Study Animals
[0080]84 Holstein steer calves of weaning age were selected from a herd without a ...
example 2
Evaluation of Cattle Receiving a DNA Immunomodulator Concurrently with or One Day After an Experimental Challenge with Mannheimia haemolytica
[0091]The purpose of this study was to determine the efficacy of the DNA immunomodulator administered to calves concurrently with or one day after an experimental challenge with Mannheimia haemolytica.
Immunomodulator
[0092]The immunomodulator used in this study was the composition described above in Example 1.
Study Animals
[0093]84 Holstein steer calves of weaning age and weighing on average about 300 lbs (136 kg) were selected from a herd without a current history of respiratory disease. Each individual calf was initially evaluated and determined to be in good health. The 84 calves were divided into seven treatment groups of 12 calves each. Only animals not vaccinated for Mannheimia haemolytica were included in the study. None of the animals had received an antimicrobial agent within 30 days prior to administration of DNA immunomodulator. The ...
example 3
Evaluation of Cattle Receiving a DNA Immunomodulator Two Days Before or Concurrently with an Experimental Challenge with Mannheimia haemolytica
[0103]The purpose of this study was to determine the efficacy of the DNA immunomodulator administered to calves two days before or concurrently with an experimental challenge with Mannheimia haemolytica.
Immunomodulator
[0104]The immunomodulator used in this study was the composition described above in Example 1.
[0105]Study Animals
[0106]96 Holstein steer calves weighing on average about 800-1000 lbs (363-454 kg) were selected from a herd without a current history of respiratory disease. Each individual calf was initially evaluated and determined to be in good health. The 96 calves were divided into eight treatment groups of 12 calves each. Only animals not vaccinated for Mannheimia haemolytica were included in the study. None of the animals had received an antimicrobial agent within 30 days prior to administration of DNA immunomodulator. The ...
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