Bergholtz B O, Thorsby E
Scand J Immunol. 1977;6(8):779-86. doi: 10.1111/j.1365-3083.1977.tb02151.x.
The proliferative response of immune human T lymphocytes to low concentrations of purified protein derivative (PPD) in vitro was found to require the presence of macrophages. By coculturing different combinations of immune T lymphocytes and allogeneic macrophages with PPD in low concentration, optimal stimulation (that is, as efficient as the autologous combinations) was shown to require HLA-D identity between the macrophages and responding T cells. Identity for HLA-A and -B appeared to be of less or no importance. It is concluded that membrane structures encoded by HLA-D or closely linked loci are involved in the human macrophage/T-lymphocyte interaction in the proliferative response to PPD, much in the same way as the Ia antigens of rodents.
研究发现,体外培养时,人免疫T淋巴细胞对低浓度纯化蛋白衍生物(PPD)的增殖反应需要巨噬细胞的存在。通过将免疫T淋巴细胞与同种异体巨噬细胞的不同组合与低浓度PPD共同培养,结果表明,最佳刺激(即与自体组合一样有效)需要巨噬细胞与反应性T细胞之间的HLA - D相同。HLA - A和 - B相同似乎不太重要或无关紧要。结论是,HLA - D或紧密连锁基因座编码的膜结构参与了人类巨噬细胞/T淋巴细胞在对PPD增殖反应中的相互作用,这与啮齿动物的Ia抗原的作用方式非常相似。