Lam H-Y, van Hoffen E, Michelsen A, Guikers K, van der Tas C H W, Bruijnzeel-Koomen C A F M, Knulst A C
Department of Dermatology/Allergology, University Medical Center Utrecht, Utrecht, The Netherlands.
Clin Exp Allergy. 2008 Jun;38(6):995-1002. doi: 10.1111/j.1365-2222.2008.02968.x. Epub 2008 Apr 1.
Studies on cow's milk allergy (CMA) in adults are scarce. Little is known about the clinical symptoms, eliciting doses (ED), and allergens involved.
The aim of this study was to analyse the clinical symptoms, ED and allergen recognition in adult CMA patients, compared with cow's milk (CM)-sensitized, but tolerant controls.
Adult CMA patients were evaluated by standardized questionnaires (n=30), skin prick tests (SPTs) and specific IgE for CM allergens (n=18), and a double-blind placebo-controlled food challenge (DBPCFC, n=10). A control group (n=25) of CM-sensitized, but tolerant adults was included.
The majority of CMA patients (20/30, 67%) reported severe symptoms. In all patients participating in DBPCFC, CMA was confirmed. ED for subjective symptoms (0.3-300 mg CM protein) were significantly lower than that for objective symptoms (300-9000 mg CM protein). The severity of CMA by history and ED was not correlated with SPT or IgE. Patients had higher SPT reactivity than controls for CM, alpha-lactalbumin and beta-lactoglobulin (P=0.002, P=0.014 and P=0.004) but not for casein. Specific IgE to CM tended to be higher (P=0.068) and IgE to casein was higher in patients than that in controls (P=0.016). No difference was observed for IgE to alpha-lactalbumin and beta-lactoglobulin.
Adult CMA is severe in nature. ED are low, starting from 0.3 mg CM protein. Patients with CMA recognize the same major allergens (casein and whey proteins) as controls, but display a stronger SPT and IgE reactivity.
关于成人牛奶过敏(CMA)的研究较少。对于其临床症状、诱发剂量(ED)及相关过敏原知之甚少。
本研究旨在分析成人CMA患者的临床症状、ED及过敏原识别情况,并与牛奶(CM)致敏但耐受的对照组进行比较。
通过标准化问卷(n = 30)、皮肤点刺试验(SPT)及针对CM过敏原的特异性IgE检测(n = 18)对成人CMA患者进行评估,并进行双盲安慰剂对照食物激发试验(DBPCFC,n = 10)。纳入一组CM致敏但耐受的成人对照组(n = 25)。
大多数CMA患者(20/30,67%)报告有严重症状。所有参与DBPCFC的患者均确诊为CMA。主观症状的ED(0.3 - 300 mg CM蛋白)显著低于客观症状的ED(300 - 9000 mg CM蛋白)。根据病史和ED判断的CMA严重程度与SPT或IgE无关。患者对于CM、α-乳白蛋白和β-乳球蛋白的SPT反应性高于对照组(P = 0.002、P = 0.014和P = 0.004),但对于酪蛋白则不然。患者针对CM的特异性IgE往往更高(P = 0.068),且针对酪蛋白的IgE高于对照组(P = 0.016)。针对α-乳白蛋白和β-乳球蛋白的IgE未观察到差异。
成人CMA本质上较为严重。ED较低,起始于0.3 mg CM蛋白。CMA患者与对照组识别相同的主要过敏原(酪蛋白和乳清蛋白),但表现出更强的SPT和IgE反应性。