Adler K A, Fenger T W, Wilson L A
Transplantation. 1980 Apr;29(4):267-73. doi: 10.1097/00007890-198004000-00001.
A xenoantiserum to human Ia antigens has been described that is capable of blocking not only stimulation in the mixed lymphocyte reaction (MLR) but also the induction of cytotoxic T lymphocytes (CTLs). Data from immunofluorescence as well as complement-dependent cytolytic assays indicate that the anti-Ia xenoantiserum is directed against B cell surface antigens. Inhibition of complement-dependent cytolysis with column fractions of B cell antigens and autoradiography of immune precipitates electrophoresed on sodium dodecyl sulfate (SDS)-polyacrylamide gels have established that the antigen detected by the xenoantiserum has characteristics of the human two-polypeptide Ia molecular complex. Allogeneic stimulator cells pretreated with anti-Ia at very low doses were unable to stimulate in the MLR and failed to induce CTLs. Neither anti-beta 2-microglobulin nor a non-HLA-associated antilymphocyte serum in similar dose ranges inhibited MLR or cell-mediated lympholysis (CML) assays. Absorption of anti-Ia xenoantiserum with B lymphoblasts, but not T lymphoblasts, removed inhibitory activity for both MLR and CML. Untreated third-party stimulator cells cocultivated with anti-Ia-pretreated stimulator cells provided stimulation in the MLR that apparently allowed partial recovery of CML against targets from the same donor as the anti-Ia-treated stimulator cells. Elimination of the helper effect, normally provided by MLR stimulation, may be one mechanism by which anti-Ia xenoantiserum prevents induction of CTLs.
已描述了一种针对人Ia抗原的异种抗血清,它不仅能够阻断混合淋巴细胞反应(MLR)中的刺激,还能阻断细胞毒性T淋巴细胞(CTL)的诱导。免疫荧光以及补体依赖性细胞溶解试验的数据表明,抗Ia异种抗血清针对的是B细胞表面抗原。用B细胞抗原的柱层析组分抑制补体依赖性细胞溶解,并对在十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶上电泳的免疫沉淀物进行放射自显影,已证实异种抗血清检测到的抗原具有人双多肽Ia分子复合物的特征。用极低剂量的抗Ia预处理的同种异体刺激细胞在MLR中无法刺激,也无法诱导CTL。在相似剂量范围内,抗β2-微球蛋白和非HLA相关的抗淋巴细胞血清均未抑制MLR或细胞介导的淋巴细胞溶解(CML)试验。用B淋巴母细胞而非T淋巴母细胞吸收抗Ia异种抗血清,可消除对MLR和CML的抑制活性。与抗Ia预处理的刺激细胞共培养的未处理第三方刺激细胞在MLR中提供了刺激,这显然使针对与抗Ia处理的刺激细胞来自同一供体的靶标的CML部分恢复。消除通常由MLR刺激提供的辅助作用可能是抗Ia异种抗血清阻止CTL诱导的一种机制。