Evans H E, Bognacki N S, Perrott L M, Glass L
J Pediatr. 1977 Apr;90(4):621-4. doi: 10.1016/s0022-3476(77)80384-3.
alpha 1-antitrypsin phenotypes were determined in cord sera of 1,010 healthy term infants of black, white and Hispanic background, by the crossed immunoelectrophoresis technique of Fagerhol and Laurell. Among the black group, M prevalence (97%) was higher than among the Hispanic group (88%). MS prevalance in the Hispanic group (6.7%) was higher than among black (1.5%) or white (3.9%) infants. Among those with an M pattern a "step" variant representing a shift of the relative amounts of protein in the major peaks of the M pattern, was found in 96% of neonates, but only among 9.8% of infants one months to two years of age and 18% among children two to ten years of age, regardless of race. Quantitative values of alpha 1-antitrypsin were not decreased among MS and MZ infants.
采用法格霍尔和劳雷尔的交叉免疫电泳技术,对1010名具有黑人、白人及西班牙裔背景的足月健康婴儿的脐带血清进行了α1 -抗胰蛋白酶表型测定。在黑人组中,M型的发生率(97%)高于西班牙裔组(88%)。西班牙裔组中MS型的发生率(6.7%)高于黑人(1.5%)或白人(3.9%)婴儿。在具有M型模式的婴儿中,一种代表M型模式主要峰中蛋白质相对含量变化的“阶梯”变体,在96%的新生儿中被发现,但在1至2岁的婴儿中仅为9.8%,在2至10岁的儿童中为18%,且与种族无关。MS型和MZ型婴儿的α1 -抗胰蛋白酶定量值并未降低。