首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Bovine colostrum as a biologic in clinical medicine: A review a Part II: Clinical studies.
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Bovine colostrum as a biologic in clinical medicine: A review a Part II: Clinical studies.

机译:牛初乳在临床医学中的应用:回顾第二部分:临床研究。

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The value of bovine colostrum as a biologic in medicine is documented in clinical trials and supported by relatively large databases containing case reports and anecdotal findings. The main actions include an antibacterial effect and modulation of the immune response. The ability of bovine colostrum concentrates (BCC are polyvalent bovine colostrum concentrates produced from the colostrums of several 100 cows) to neutralize lipopolysaccharides, i.e. endotoxins arising from Gram-negative bacterial pathogens and to inhibit enterogenic endotoxemia in animal models as shown in the last review to have its counterpart in patient therapy. Clinical trials with BCC provide evidence that oral application reduces the influx of LPS from the gut and this appears to be a major mechanism underlying its therapeutic effect in patients at risk for Gram-negative septic shock; data from two well-controlled clinical studies with a total of 100 surgical patients have shown that the inhibition of intestinal LPS absorption measured after the application of BCC not only reduced the LPS levels in the peripheral blood but also inflammatory parameters like IL-6 and CRP were found to be diminished. The usual daily dose of the commercially available BCC preparation, LactobinA(R) (LC1) is 10 a 20 g daily, but higher doses can be used in the majority of patients because of the low incidence of intolerance problems. In chronic diarrhea involving severe forms of secondary immunodeficiencies, patients receiving LC1 were disease-free for about 4 weeks but the response may be lower in patients with AIDS. BCC is effective in infants with hemorrhagic diarrhea caused by infections with enterohemorrhagic E. coli and reduces the likelihood of the disease progressing to a hemolytic uremic syndrome. The safety of newer BCC products obtained from BSE-free regions seems now beyond contention. In the case of LC1, which was used as a commercial dietary foodstuff in Germany until 1992 and tested in three Phase 1 and 5 clinical studies (two trials in patients with secondary immunodeficiencies, one in surgical patients with gastrointestinal disorders, one in patients undergoing open heart surgery and one in pediatric patients with EHEC infections), there were no cases of BSE-associated disease such as the new variant of Creutzfeldt-Jakob disease. Side effects of clinical relevance are limited to possible intolerance to lactose and sensitivity to milk proteins as these are also present in many commonly used foodstuffs. Important synergistic actions with conventional drug therapies have been observed with BCC including a reduction in LPS plasma levels in patients with Gram-negative bacterial infections treated with bactericidal antibiotics. In healthy persons there are only small concentrations of LPS detectable in peripheral blood (normal values: 3 a 10 pg/ ml plasma, i.e. approximately 0.1 EU/ml). In contrast, elevated systemic levels with concentrations > 300 pg/ml are common in patients with severe Gram-negative sepsis and septic shock. Raised LPS levelsoccur mainly in patients with Gram-negative bacterial infections who have been treated with bacteriocidal antibiotics. The LPS-lowering effects of BCC are probably due to the numerous active components present in BCC which have their origin in the innate humoral and adaptive immune system of their biologic source, the cow.
机译:牛初乳作为医学生物制剂的价值已在临床试验中得到证明,并得到包含病例报告和轶事发现的相对较大的数据库的支持。主要作用包括抗菌作用和免疫应答的调节。牛初乳浓缩物(BCC是从几百头牛的初乳中产生的多价牛初乳浓缩物)中和脂多糖(即革兰氏阴性细菌病原体产生的内毒素和抑制动物模型中肠源性内毒素血症)的能力。在患者治疗方面有相应的选择BCC的临床试验提供了证据,表明口服可减少肠道内LPS的流入,这似乎是潜在的革兰氏阴性败血性休克患者治疗效果的主要机制。来自两项涉及100例外科手术患者的良好对照临床研究的数据表明,应用BCC后对肠道LPS吸收的抑制作用不仅降低了外周血中的LPS水平,而且还降低了炎症参数,例如IL-6和CRP被发现减少。市售BCC制剂LactobinA(L1)的通常每日剂量为10至20 g每日,但由于不耐受问题的发生率较低,因此大多数患者可以使用更高剂量。在涉及严重形式的继发性免疫缺陷的慢性腹泻中,接受LC1的患者无病约4周,但艾滋病患者的反应可能较低。 BCC对因肠出血性大肠杆菌感染引起的出血性腹泻有效,并降低了疾病发展为溶血性尿毒症综合征的可能性。从无疯牛病地区获得的较新的BCC产品的安全性现在似乎已成问题。以LC1为例,直到1992年在德国一直用作商业饮食食品,并在三项1期和5期临床研究中进行了测试(两项针对继发性免疫缺陷患者的试验,一项针对胃肠道疾病的外科手术患者,一项针对开放性消化道疾病的患者)心脏手术和小儿EHEC感染患者之一),没有与BSE相关的疾病,如Creutzfeldt-Jakob疾病的新变种。临床相关性的副作用仅限于对乳糖的不耐受性和对乳蛋白的敏感性,因为它们在许多常用食品中也存在。已观察到BCC与常规药物疗法具有重要的协同作用,包括用杀菌抗生素治疗的革兰氏阴性细菌感染患者的LPS血浆水平降低。在健康人中,外周血中仅可检测到少量LPS(正常值:3至10 pg / ml血浆,即约0.1 EU / ml)。相反,严重革兰氏阴性脓毒症和败血性休克的患者体内浓度高于300 pg / ml的全身水平升高很常见。 LPS水平升高主要发生在已用杀菌抗生素治疗的革兰氏阴性细菌感染患者中。 BCC降低LPS的作用可能归因于BCC中存在的许多活性成分,这些活性成分起源于其生物来源(母牛)的固有体液和适应性免疫系统。

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