Herbert P N, Hyams J S, Bernier D N, Berman M M, Saritelli A L, Lynch K M, Nichols A V, Forte T M
J Clin Invest. 1985 Aug;76(2):403-12. doi: 10.1172/JCI111986.
We describe a child, the issue of phenotypically normal parents, who had fat malabsorption, both intestinal and hepatic steatosis, and serum cholesterol and triglyceride concentrations of 38 and 63 mg/dl, respectively. Lipoprotein electrophoresis, Ouchterlony double diffusion, and electron microscopy demonstrated that normal low density lipoproteins (LDL: 1.006 less than rho less than 1.063 g/ml) were absent. Lipoprotein particles in the rho less than 1.006-g/ml fraction were triglyceride rich, very large (93.2 +/- 35.1 nm), and contained the B-48 but not the B-100 apoprotein; both species of apolipoprotein (apo) B were found in the parents' lipoproteins. These chylomicrons and chylomicron remnants were present even in the patient's fasting plasma, which suggested prolonged dietary fat absorption. Plasma levels of high density lipoprotein lipids and proteins were low, and the phosphatidylcholine/sphingomyelin ratio was reduced as in typical abetalipoproteinemia. The monosialylated form of apo C-III was not identified on polyacrylamide gel electrophoresis, which suggested that this protein was elaborated only with very low density lipoproteins (VLDL). A radioimmunoassay for apo B employing a polyclonal antisera to plasma LDL gave apparent plasma apo B levels of 0.6, 66, and 57 mg/dl in the patient and his father and mother, respectively. The displacement curve generated by the parents' VLDL and LDL did not did not differ from control lipoproteins. The patient's chylomicron-chylomicron remnant fraction displaced normal LDL over the entire radioimmunoassay range, but the efficiency of displacement was strikingly less than with B-100 containing lipoproteins. If the patient's B-48 protein is not qualitatively abnormal, these results confirm very limited immunochemical cross-reactivity between at least one major epitope on B-100 and the epitopes expressed on B-48. The apo B defect in this patient appears to be recessive. It abolishes B-100 production and may additionally limit the formation of B-48.
我们描述了一个孩子,其父母表型正常,该患儿存在脂肪吸收不良、肠道和肝脏脂肪变性,血清胆固醇和甘油三酯浓度分别为38和63mg/dl。脂蛋白电泳、双向琼脂扩散试验和电子显微镜检查显示不存在正常的低密度脂蛋白(LDL:1.006<ρ<1.063g/ml)。ρ<1.006g/ml部分的脂蛋白颗粒富含甘油三酯,非常大(93.2±35.1nm),含有B-48载脂蛋白但不含B-100载脂蛋白;两种载脂蛋白B(apo B)均存在于父母的脂蛋白中。即使在患者的空腹血浆中也存在这些乳糜微粒和乳糜微粒残粒,这提示膳食脂肪吸收延长。血浆高密度脂蛋白脂质和蛋白质水平较低,磷脂酰胆碱/鞘磷脂比值降低,如同典型的无β脂蛋白血症。在聚丙烯酰胺凝胶电泳上未鉴定出单唾液酸化形式的apo C-III,这提示该蛋白仅在极低密度脂蛋白(VLDL)中合成。使用针对血浆LDL的多克隆抗血清进行的apo B放射免疫测定显示,患者及其父亲和母亲的血浆apo B水平分别为0.6、66和57mg/dl。父母的VLDL和LDL产生的置换曲线与对照脂蛋白无差异。患者的乳糜微粒-乳糜微粒残粒部分在整个放射免疫测定范围内可置换正常LDL,但置换效率明显低于含B-100的脂蛋白。如果患者的B-48蛋白在质量上无异常,这些结果证实至少一个B-100主要表位与B-48上表达的表位之间的免疫化学交叉反应非常有限。该患者的apo B缺陷似乎是隐性的。它消除了B-100的产生,并且可能还限制了B-48的形成。