Butler W T, Rossen R D, Waldmann T A
J Clin Invest. 1967 Dec;46(12):1883-93. doi: 10.1172/JCI105678.
Experiments were done to investigate mechanisms of appearance of both 7 S and 11 S IgA in nasal secretions. Three IgA preparations, (a) 11 S IgA from nasal secretions, (b) 7 S IgA from homologous serum, and (c) 7 S IgA from autologous serum, were isolated, labeled, and injected intravenously into volunteers. The rate of disappearance from plasma and the extent and nature of their appearance in nasal secretions were examined in detail. After intravenous injection, 11 S IgA from nasal secretions disappeared rapidly from plasma. However, only negligible amounts of 11 S IgA were detected in nasal secretion, which suggested that rapid selective secretion of circulating 11 S IgA does not occur as a mechanism of IgA accumulation in nasal secretions. Both the homologous and autologous 7 S IgA preparations disappeared from plasma at a normal rate, and both appeared in nasal secretions unchanged in sedimentation behavior. The specific activity of IgA in nasal secretions, when related to the total IgA concentration, was about 30-fold less than that in serum. When related to only the 7 S IgA concentration of nasal secretions, the specific activity was about one-half that of serum. These studies are consistent with the following hypotheses: (a) circulating 7 S IgA is a source of part of the 7 S IgA found in nasal secretions. The remainder of the nasal secretion 7 S IgA may be synthesized locally in the tissues of the upper respiratory tract; (b) 11 S IgA in nasal secretions is not assembled from serum 7 S IgA components; and (c) 11 S IgA in nasal secretions is synthesized de novo in the tissues of the upper respiratory tract.
开展实验以研究7S和11S IgA在鼻分泌物中出现的机制。分离出三种IgA制剂,(a)来自鼻分泌物的11S IgA,(b)来自同源血清的7S IgA,以及(c)来自自体血清的7S IgA,进行标记后静脉注射到志愿者体内。详细检查了它们从血浆中消失的速率以及在鼻分泌物中出现的程度和性质。静脉注射后,来自鼻分泌物的11S IgA从血浆中迅速消失。然而,在鼻分泌物中仅检测到极少量的11S IgA,这表明循环中的11S IgA快速选择性分泌并非鼻分泌物中IgA积累的机制。同源和自体的7S IgA制剂均以正常速率从血浆中消失,且二者在鼻分泌物中的沉降行为均未改变。当与总IgA浓度相关时,鼻分泌物中IgA的比活性比血清中的约低30倍。当仅与鼻分泌物中的7S IgA浓度相关时,比活性约为血清的一半。这些研究与以下假设一致:(a)循环中的7S IgA是鼻分泌物中部分7S IgA的来源。鼻分泌物中其余的7S IgA可能在上呼吸道组织中局部合成;(b)鼻分泌物中的11S IgA不是由血清7S IgA成分组装而成;(c)鼻分泌物中的11S IgA是在上呼吸道组织中重新合成的。