Høst A
Department of Pediatrics, Odense University Hospital, Denmark.
Pediatr Allergy Immunol. 1994;5(5 Suppl):1-36.
Reproducible clinically abnormal reactions to cow's milk protein (CMP) may be due to the interaction between one or more milk proteins and one or more immune mechanisms, possibly any of the four basic types of hypersensitivity reactions. At present, evidence for type I, III and IV reactions against CMP has been demonstrated. Immunologically mediated reactions, mainly immediate IgE-mediated reactions are defined as cow's milk protein allergy (CMPA). Non immunologically reactions against CMP are defined as cow's milk protein intolerance (CMPI). Many studies on "cow's milk allergy'" have not investigated the immunological basis of the clinical reactions. It is not possible to differentiate between CMPA and CMPI solely on clinical symptoms. No single laboratory test is diagnostic of CMPA/CMPI. Therefore, the diagnosis still has to be based on strict well-defined elimination and milk challenge procedures. Before 1950 CMPA/CMPI was rarely diagnosed. Since 1970 widely varying estimates of the incidence from 1.8% to 7.5% have been reported, mainly reflecting differences in diagnostic criteria and study design. Based on strict diagnostic criteria the incidence of confirmed CMPA/CMPI in infancy seems to be about 2-5% in developed countries. Symptoms suggestive of CMPA/CMPI may be encountered in about 5-15% of infants emphasizing the importance of controlled elimination/milk challenge. In breastfed infants reproducible clinical reactions to CMP in human milk have been reported in about 0.5%. Most infants with CMPA/CMPI develop symptoms before one month of age, often within one week after introduction of cow's milk based formula. The majority have > or = 2 symptoms and symptoms from > or = 2 organ systems. About 50%-70% have cutaneous symptoms, 50-60% gastrointestinal symptoms, and about 20-30% respiratory symptoms. In exclusively breast-fed infants with CMPA/CMPI severe atopic eczema is a predominant symptom. Debut of CMPA/CMPI after 12 months is extremely rare. The basic treatment is complete avoidance of CMP. In infancy a proven hypoallergenic CM substitute is needed. Due to clinically important residual allergenicity in some hypoallergenic formulae controlled clinical testing is necessary in each case before use. Goat's milk proteins share identity with CMP Raw untreated cow's milk and unhomogenized cow's milk is as allergenic as normal pasteurized and homogenized milk products. The prognosis of CMPA/CMPI is good with a remission rate about 45-50% at one year, 60-75% at two years, and 85-90% at three years. Associated adverse reactions to other foods develop in about 50%, and allergy against inhalants in 50-80% before puberty.(ABSTRACT TRUNCATED AT 400 WORDS)
对牛奶蛋白(CMP)产生可重复的临床异常反应可能是由于一种或多种牛奶蛋白与一种或多种免疫机制之间的相互作用,可能是四种基本类型的超敏反应中的任何一种。目前,针对CMP的I型、III型和IV型反应的证据已得到证实。免疫介导的反应,主要是即刻IgE介导的反应被定义为牛奶蛋白过敏(CMPA)。对CMP的非免疫反应被定义为牛奶蛋白不耐受(CMPI)。许多关于“牛奶过敏”的研究并未调查临床反应的免疫基础。仅根据临床症状无法区分CMPA和CMPI。没有单一的实验室检查可诊断CMPA/CMPI。因此,诊断仍需基于严格明确的排除和牛奶激发程序。1950年以前,CMPA/CMPI很少被诊断出来。自1970年以来,报告的发病率差异很大,从1.8%到7.5%不等,主要反映了诊断标准和研究设计的差异。根据严格的诊断标准,发达国家婴儿中确诊的CMPA/CMPI发病率似乎约为2%-5%。在约5%-15%的婴儿中可能会出现提示CMPA/CMPI的症状,这强调了进行对照排除/牛奶激发试验的重要性。在母乳喂养的婴儿中,据报道对人乳中CMP产生可重复临床反应的比例约为0.5%。大多数CMPA/CMPI婴儿在1月龄前出现症状,通常在引入基于牛奶的配方奶后一周内。大多数婴儿有≥2种症状,且症状来自≥2个器官系统。约50%-70%有皮肤症状,50%-60%有胃肠道症状,约20%-30%有呼吸道症状。在纯母乳喂养且患有CMPA/CMPI的婴儿中,重度特应性皮炎是主要症状。12个月后出现CMPA/CMPI极为罕见。基本治疗方法是完全避免CMP。在婴儿期,需要一种经过验证的低敏性CMP替代品。由于某些低敏配方奶存在临床上重要的残留致敏性,每种配方奶在使用前都需要进行对照临床试验。山羊奶蛋白与CMP有相同的抗原性。未经处理的生牛奶和未均质化的牛奶与正常巴氏杀菌和均质化的奶制品一样具有致敏性。CMPA/CMPI的预后良好,1年缓解率约为45%-50%,2年为60%-75%,3年为85%-90%。约50%会出现对其他食物的相关不良反应,青春期前对吸入性过敏原过敏的比例为50%-80%。(摘要截选至400字)