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患有肺含铁血黄素沉着症儿童的C1q结合免疫复合物及其他免疫学研究。

C1q-binding immune complexes and other immunological studies in children with pulmonary hemosiderosis.

作者信息

Blanco A, Solís P, Gómez S, Linares P, Sánchez Villares E

出版信息

Allergol Immunopathol (Madr). 1984 Jan-Feb;12(1):37-44.

PMID:6375320
Abstract

We report immunological studies performed in 19 sera from 4 children with idiopathic pulmonary hemosiderosis (IPH). Circulating C1q binding immune complexes (IC) were found in 3/4 of the patients during the acute phase. One child showed IC in 4 consecutive crises but they disappeared very rapidly (within 36 hours). Only one serum was positive after acute crisis. In one patient who had 2 episodes. IC were never detected. Precipitation with 2% polyethylene glycol did not correlate with the C1q binding assay. Pulmonary biopsy was available in just one patient and neither immunoglobulins nor complement were found by immunofluorescence. IgA, IgM, IgE, C4 or B factor abnormalities were only occasionally seen. Antinuclear, anti-reticulin and anti-alveolar basement membrane antibody test were always negative. Precipitins against cow's milk proteins were not detected. Seric IC could be primary or secondary to macrophage blockade by hemosiderin. Even in this case, it is well known that circulating IC can perform some immunological actions by interacting with cell receptors or releasing active mediators. In the future, the possibility that IC could contribute to IPH pathogenesis, or modify the treatment response must be taken into account.

摘要

我们报告了对4名患有特发性肺含铁血黄素沉着症(IPH)儿童的19份血清进行的免疫学研究。在急性期,4名患者中有3名检测到循环C1q结合免疫复合物(IC)。一名儿童在连续4次发作时均检测到IC,但它们消失得非常迅速(36小时内)。急性发作后只有一份血清呈阳性。一名有2次发作的患者从未检测到IC。用2%聚乙二醇沉淀法与C1q结合试验结果不相关。仅一名患者进行了肺活检,免疫荧光检查未发现免疫球蛋白和补体。仅偶尔见到IgA、IgM、IgE、C4或B因子异常。抗核抗体、抗网状纤维抗体和抗肺泡基底膜抗体检测始终为阴性。未检测到针对牛奶蛋白的沉淀素。血清IC可能是原发性的,也可能是含铁血黄素对巨噬细胞阻滞继发的。即使在这种情况下,众所周知,循环IC可通过与细胞受体相互作用或释放活性介质发挥一些免疫作用。未来,必须考虑IC可能促成IPH发病机制或改变治疗反应的可能性。

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