Gorenberg D J, Daniele R P
Am Rev Respir Dis. 1976 Dec;114(6):1099-105. doi: 10.1164/arrd.1976.114.6.1099.
To gain insight into the structure of the lung's immune system, the identity and function of immunocompetent cells in the broncho-alveolar air spaces and tracheobronchial lymph nodes of normal guinea pigs were examined. Guinea pig thymus-derived (T) lymphocytes (mediators of cellular immunity) were identified by their ability to form rosettes with rabbit erythrocytes (E rosettes). Bone marrow-derived (B) lymphocytes (mediators of humoral immunity) were identified by their ability to form rosettes with sheep erythrocytes sensitized with antibody and complement (EAC rosettes) and by the presence of surface immunoglobulin, detected by direct immunofluorescence. Total lung lavage yielded 14+/-5.0 X 10(6) (mean +/- SD) cells. There were 68+/-5 per cent cells of the monocyte-macrophage series as judged by morphology, the ingestion of latex particles, and the uptake of neutral red; 20+/-9 per cent were eosinophils, and 12+/-5 per cent were lymphocytes. Stable populations of T and B lymphocytes were recovered from guinea pig airways and tracheobronchial lymph nodes. T cells represented 76 per cent of lymphocytes from the airways and 64 per cent of lymphocytes in tracheobronchial lymph node; B cells equalled 14 per cent and 30 per cent, respectively. The functional potential of T cells present in the lung and tracheobronchial lymph node was demonstrated by their proliferative response to phytohemagglutinin. These results indicated that, although macrophages are the predominant cell type, viable T and B lymphocytes are present in the guinea pig broncho-alveolar air space. The composition of these cells is comparable to what has been observed in normal human lungs and provides preliminary evidence that the guinea pig may be a useful model for humans. This report also describes a method using 2 vital stains whereby macrophages, lymphocytes, and rosetted lymphocytes can be distinguished in unseparated cell suspensions prepared from bronchial aspirates.
为深入了解肺免疫系统的结构,对正常豚鼠支气管肺泡气腔和气管支气管淋巴结中免疫活性细胞的特性及功能进行了研究。豚鼠胸腺来源的(T)淋巴细胞(细胞免疫的介质)通过其与兔红细胞形成玫瑰花结的能力(E玫瑰花结)来鉴定。骨髓来源的(B)淋巴细胞(体液免疫的介质)通过其与用抗体和补体致敏的绵羊红细胞形成玫瑰花结的能力(EAC玫瑰花结)以及通过直接免疫荧光检测到的表面免疫球蛋白的存在来鉴定。全肺灌洗产生了14±5.0×10⁶(平均值±标准差)个细胞。根据形态、乳胶颗粒摄取和中性红摄取判断,单核细胞 - 巨噬细胞系列细胞占68±5%;嗜酸性粒细胞占20±9%,淋巴细胞占12±5%。从豚鼠气道和气管支气管淋巴结中回收了稳定的T和B淋巴细胞群体。T细胞占气道淋巴细胞的76%,占气管支气管淋巴结淋巴细胞的64%;B细胞分别占14%和30%。肺和气管支气管淋巴结中存在的T细胞的功能潜力通过其对植物血凝素的增殖反应得以证明。这些结果表明,尽管巨噬细胞是主要的细胞类型,但豚鼠支气管肺泡气腔中存在有活力的T和B淋巴细胞。这些细胞的组成与在正常人类肺中观察到的情况相当,并提供了初步证据表明豚鼠可能是人类的有用模型。本报告还描述了一种使用两种活体染色剂的方法,通过该方法可以在由支气管吸出物制备的未分离细胞悬液中区分巨噬细胞、淋巴细胞和形成玫瑰花结的淋巴细胞。