Goldberg L S, Douglas S D, Fudenberg H H
Clin Exp Immunol. 1969 May;4(5):579-84.
Sera and saliva from nine adult subjects with acquired agammaglobulinaemia and from two individuals with a selective absence of γA were studied for γA and secretory γA content. In all subjects, except for one (B.Cr.), secretory γA was detected in saliva when γA was demonstrable by radial diffusion in serum, and salivary secretory piece alone was found in the absence of serum γA. Saliva B.Cr. contained both γA and free secretory piece, whereas the serum from this patient appeared to lack γA. However, when tested by quantitative complement fixation, a small amount of serum γA was detected. Chromatographic separation and subsequent immunological testing of saliva B.Cr. revealed the presence of secretory γA, secretory piece, and a small amount of serum-type γA. Severity of sinopulmonary infections in these subjects did not correlate with the presence or absence of secretory γA. These observations further substantiate that the production of serum and secretory γA is controlled by similar mechanisms, and that a quantitative defect in secretory γA production does not by itself account for the presence of sinopulmonary disease.
对9名获得性无丙种球蛋白血症成年患者的血清和唾液以及2名选择性缺乏γA的个体的血清和唾液进行了γA和分泌型γA含量研究。在所有受试者中,除了一名受试者(B.Cr.)外,当通过血清中的单向扩散证明存在γA时,在唾液中检测到了分泌型γA,并且在没有血清γA的情况下仅发现了唾液分泌片。唾液B.Cr.中同时含有γA和游离分泌片,而该患者的血清似乎缺乏γA。然而,通过定量补体结合试验检测时,发现了少量血清γA。对唾液B.Cr.进行色谱分离并随后进行免疫学检测,结果显示存在分泌型γA、分泌片和少量血清型γA。这些受试者鼻窦肺部感染的严重程度与分泌型γA的有无无关。这些观察结果进一步证实,血清γA和分泌型γA的产生受相似机制控制,并且分泌型γA产生的定量缺陷本身并不能解释鼻窦肺部疾病的存在。