Kumar S N, Seelig L L, Head J R
J Reprod Immunol. 1985 Nov;8(2-3):235-48. doi: 10.1016/0165-0378(85)90043-9.
The maternal component in the transfer of cellular immunity from the mother to the neonate during lactation was investigated by analyzing the migration of adoptively transferred T-lymphocytes to the mammary gland and into the milk of lactating rats. A T-enriched cell population, containing less than 2.5% of contaminating B-cells, was obtained from mesenteric and peripheral lymph node cells of donor rats by removing B-cells with a panning technique. The T-enriched cells, radiolabeled with [3H]uridine, were injected intravenously into syngeneic lactating females, between 1 and 4 days post-partum. Samples of mesenteric and cervical lymph nodes, spleen, Peyer's patches, small intestine, and mammary gland taken at 48 h and milk obtained at 24 and 48 h were processed for scintillation counting and autoradiography. A large portion of the injected T-cells migrated to T-dependent lymphoid areas (the paracortical and medullary regions of the mesenteric and cervical lymph nodes and the Peyer's patches) and a substantial number also migrated into the small intestine and mammary gland, although the frequency of cells per high-power field was lower than in the lymph nodes. However, total counts of activity recovered were significantly higher in the small intestine and mammary gland than in either the mesenteric or cervical groups of lymph nodes. The distribution of the T-cells within the mammary gland showed a relative predominance of labeled cells in the connective tissue adjacent to the alveolar secretory cells, with a small percentage of cells present within the mammary epithelium. The direct transfer of T-cells through the alveolar epithelium was demonstrated by the presence of labeled cells in milk. These results substantiate that a significant number of T-lymphocytes migrate not only to the mammary gland during lactation but also into milk. These cells may play a passive regulatory or inductive role within the mammary gland or an active role in the maternal-to-neonatal transfer of immunity.
通过分析过继转移的T淋巴细胞在哺乳期大鼠乳腺中的迁移以及进入乳汁的情况,研究了哺乳期母体向新生儿传递细胞免疫过程中的母体成分。通过淘选技术去除B细胞,从供体大鼠的肠系膜和外周淋巴结细胞中获得富含T细胞的群体,其中污染的B细胞少于2.5%。用[3H]尿苷进行放射性标记的富含T细胞的细胞,在产后1至4天静脉注射到同基因的哺乳期雌性大鼠体内。在48小时采集肠系膜和颈部淋巴结、脾脏、派尔集合淋巴结、小肠和乳腺的样本,并在24小时和48小时采集乳汁样本,进行闪烁计数和放射自显影处理。大部分注入的T细胞迁移到T细胞依赖的淋巴区域(肠系膜和颈部淋巴结以及派尔集合淋巴结的副皮质区和髓质区),并且相当数量的T细胞也迁移到小肠和乳腺,尽管每高倍视野中的细胞频率低于淋巴结中的频率。然而,小肠和乳腺中回收的活性总计数明显高于肠系膜或颈部淋巴结组。乳腺内T细胞的分布显示,与肺泡分泌细胞相邻的结缔组织中标记细胞相对占优势,乳腺上皮内有一小部分细胞。乳汁中存在标记细胞证明了T细胞通过肺泡上皮的直接转移。这些结果证实,在哺乳期大量T淋巴细胞不仅迁移到乳腺,而且进入乳汁。这些细胞可能在乳腺内发挥被动调节或诱导作用,或者在母体向新生儿的免疫转移中发挥积极作用。