Frew A J, Kay A B
Department of Respiratory Physiology, City General Hospital, Stoke-on-Trent, England.
Clin Exp Immunol. 1991 Jul;85(1):70-4. doi: 10.1111/j.1365-2249.1991.tb05684.x.
There still remains some controversy regarding the possible role of immune complexes in the pathogenesis of the late-phase skin reaction (LPSR). To assess this, skin biopsies were obtained from LPSR induced in atopic human subjects 6, 24 and 48 h after allergen challenge. Cryostat sections were stained by direct immunofluorescence for the presence of fibrinogen, immunoglobulin classes IgM and IgG and for the complement components C1q and C3c. Complement components were observed in only two of the 29 biopsies studied. In both instances, only C3c was detected. One of these subjects also had unequivocal IgG staining at 6 h. IgM staining was detected in two out of 10 subjects at 6 h but no significant deposition of immunoglobulins could be found at 24 or 48 h. Fibrinogen deposition was observed in about half of the biopsies at each time-point. This study suggests that substantial complement and immunoglobulin deposition are not overt features of the allergen-induced LPSR, although the presence of small amounts of immune complexes, below the sensitivity of the method employed cannot be excluded. Fibrin deposition occurs in the LPSR but does not appear to be a prerequisite for LPSR development.
关于免疫复合物在迟发性皮肤反应(LPSR)发病机制中可能发挥的作用,仍存在一些争议。为评估这一点,在变应原激发后6小时、24小时和48小时,从特应性人类受试者诱发的LPSR中获取皮肤活检样本。冰冻切片通过直接免疫荧光染色检测纤维蛋白原、免疫球蛋白IgM和IgG类别以及补体成分C1q和C3c的存在情况。在所研究的29份活检样本中,仅在两份样本中观察到补体成分。在这两个样本中,均仅检测到C3c。其中一名受试者在6小时时也有明确的IgG染色。在10名受试者中的两名在6小时时检测到IgM染色,但在24小时或48小时时未发现免疫球蛋白有明显沉积。在每个时间点,约一半的活检样本中观察到纤维蛋白原沉积。这项研究表明,大量补体和免疫球蛋白沉积并非变应原诱导的LPSR的明显特征,尽管不能排除存在少量低于所用方法检测灵敏度的免疫复合物。纤维蛋白沉积发生在LPSR中,但似乎不是LPSR发生的先决条件。