Havenith C E, Breedijk A J, Betjes M G, Calame W, Beelen R H, Hoefsmit E C
Department of Cell Biology, Vrije Universiteit, Amsterdam, The Netherlands.
Am J Respir Cell Mol Biol. 1993 Mar;8(3):319-24. doi: 10.1165/ajrcmb/8.3.319.
In the present study, splenic dendritic cells (DC) and alveolar macrophages (AM) were pulsed with antigen in vitro and subsequently intratracheally instilled to test whether these cells have the capacity to sensitize T cells in the draining lymph nodes of the lung. The data demonstrate that antigen-pulsed DC, instilled in the bronchoalveolar lumen, induce antigen-specific T cell priming in vivo in the draining lymph nodes. T cell priming is only seen with viable but not with killed antigen-pulsed DC. Amounts as low as 5 x 10(3) to 10 x 10(3) cells can still induce some responsiveness. In addition, it was found that instillation of viable as well as killed pulsed Ia-negative AM also leads to T cell priming, although about 10 times higher numbers of cells had to be used in comparison with DC. The results suggest that DC instilled in the bronchoalveolar lumen present antigen directly to naive T cells, whereas for AM other mechanisms are involved.
在本研究中,脾树突状细胞(DC)和肺泡巨噬细胞(AM)在体外经抗原脉冲处理,随后经气管内注入,以测试这些细胞是否有能力在肺引流淋巴结中致敏T细胞。数据表明,注入支气管肺泡腔内的经抗原脉冲处理的DC在体内引流淋巴结中诱导抗原特异性T细胞致敏。仅在活的而非灭活的经抗原脉冲处理的DC中观察到T细胞致敏。低至5×10³至10×10³个细胞的量仍可诱导一定的反应性。此外,还发现注入活的以及灭活的经脉冲处理的Ia阴性AM也会导致T细胞致敏,尽管与DC相比,所需细胞数量约高10倍。结果表明,注入支气管肺泡腔内的DC直接将抗原呈递给幼稚T细胞,而对于AM则涉及其他机制。