Ahlstedt S, Carlsson B, Fällström S P, Hanson L A, Holmgren J, Lidin-Janson G, Lindblad B S, Jodal U, Kaijser B, Solh-Akerlund A, Wadsworth C
Ciba Found Symp. 1977(46):115-34. doi: 10.1002/9780470720288.ch6.
Ingestion of Escherichia coli O83 bacteria by adults resulted in a transient irregular colonization leading to a serum antibody response in only four out of 14 cases examined. In all of three pregnant women, however, IgA antibodies against E. coli O83 antigen were released from colostral cells after similar bacterial ingestion although no serum antibody response was noted. The findings indicate a link between the antigenic exposure to the gut and secretory antibodies of the IgA class, presumably locally formed in the mammary gland. Antibodies of the secretory IgA class registered in colostrum may, at least partly, reflect the antigenic exposure of the gut. These antibodies are probably important in protecting against E. coli infections in the neonate, as suggested by the findings of antibodies in human milk against O and K antigens of non-enteropathogenic as well as enteropathogenic serotypes of E. coli. Furthermore, in milk of women from low socio-economic groups in Pakistan, neutralizing antibodies were present against enterotoxins of E. coli bacteria and occasionally against Vibrio cholerae enterotoxins. In addition, secretory IgA antibodies against food proteins were detected in human milk. This suggests that intestinal exposure to such antigens could stimulate a local immune response in the gut resulting in triggered lymphoid cells homing to the mammary gland. These human milk secretory IgA antibodies against bovine milk proteins may help to prevent cow's milk allergy in infants on mixed feeding, since these infants tend to have a lower serum antibody response to cow's milk proteins than infants fed mostly artificially. Furthermore, children suffering from cow's milk protein intolerance and gluten enteropathy may have higher serum levels of antibody to cow's milk protein antigens than normal children, possibly reflecting increased permeability of the intestinal mucosa for various antigens.
成年人摄入大肠杆菌O83后会导致短暂的不规则定植,在14例受检病例中只有4例产生血清抗体反应。然而,在所有3名孕妇中,摄入类似细菌后,初乳细胞会释放出针对大肠杆菌O83抗原的IgA抗体,尽管未观察到血清抗体反应。这些发现表明肠道抗原暴露与IgA类分泌抗体之间存在联系,推测这些抗体是在乳腺局部形成的。初乳中检测到的分泌型IgA类抗体可能至少部分反映了肠道的抗原暴露情况。这些抗体可能对预防新生儿感染大肠杆菌很重要,正如人乳中存在针对非致病性和致病性大肠杆菌血清型的O和K抗原的抗体这一发现所表明的那样。此外,在巴基斯坦社会经济地位较低群体的妇女乳汁中,存在针对大肠杆菌肠毒素的中和抗体,偶尔也存在针对霍乱弧菌肠毒素的中和抗体。另外,在人乳中检测到针对食物蛋白的分泌型IgA抗体。这表明肠道接触此类抗原可刺激肠道局部免疫反应,导致触发的淋巴细胞归巢至乳腺。这些针对牛乳蛋白的人乳分泌型IgA抗体可能有助于预防混合喂养婴儿的牛奶过敏,因为这些婴儿对牛乳蛋白的血清抗体反应往往低于主要采用人工喂养的婴儿。此外,患有牛乳蛋白不耐受和麸质肠病的儿童,其血清中针对牛乳蛋白抗原的抗体水平可能高于正常儿童,这可能反映出肠道黏膜对各种抗原的通透性增加。