Yazaki M, Takahashi T, Andho M, Akatsuka Y, Ito T, Miyake Y, Ito Y, Nakamura S, Wada Y
Department of Pediatrics, Nagoya City University Medical School, Nagoya, Japan.
Bone Marrow Transplant. 1999 Jul;24(2):129-37. doi: 10.1038/sj.bmt.1701856.
Bulk cytotoxic T lymphocytes (CTL) were generated by in vitro stimulation of BMT donor lymphocytes with Philadelphia chromosome (Ph)-positive leukemic cells from an HLA-identical sibling patient. CTL were cytotoxic against the patient's leukemic cells as well as the EBV-lymphoblastoid cell line (EBV-LCL) generated from the patient's cells, suggesting that they recognize a minor histocompatibility antigen (mHAg). Subsequently, several CTL lines were established by a limiting dilution method and analyzed. One of these CTL lines, 16C12 CTL which used a single TCRbetaV3S1 for CD8 cells, lysed HLA-A31-positive leukemic cells and EBV-LCL, but not fibroblasts. The cytotoxicity against the patient's leukemic cells and EBV-LCL was blocked by anti-HLA-A31 moAb, anti-HLA-class I moAb, and anti-CD8 moAb, suggesting that this mHAg was presented with HLA-A31. The antigen recognized by 16C12 CTL seemed to be a novel mHAg, since HLA-A31 restricted antigen has not been reported to date and 16C12 CTL showed no cytotoxicity against EBV-LCL which probably express known mHAgs. CTL detecting this mHAg may play an important role in the GVL effect in HLA-A31-positive BMT patients.
通过用来自 HLA 相同的同胞患者的费城染色体(Ph)阳性白血病细胞体外刺激骨髓移植(BMT)供体淋巴细胞,产生大量细胞毒性 T 淋巴细胞(CTL)。CTL 对患者的白血病细胞以及由患者细胞产生的 EBV 淋巴母细胞系(EBV-LCL)具有细胞毒性,这表明它们识别一种次要组织相容性抗原(mHAg)。随后,通过有限稀释法建立了几个 CTL 系并进行分析。其中一个 CTL 系,即 16C12 CTL,其 CD8 细胞使用单一 TCRbetaV3S1,可裂解 HLA-A31 阳性白血病细胞和 EBV-LCL,但不能裂解成纤维细胞。针对患者白血病细胞和 EBV-LCL 的细胞毒性被抗 HLA-A31 单克隆抗体、抗 HLA-I 类单克隆抗体和抗 CD8 单克隆抗体阻断,这表明这种 mHAg 是与 HLA-A31 呈递的。16C12 CTL 识别的抗原似乎是一种新型 mHAg,因为迄今为止尚未报道 HLA-A31 限制性抗原,并且 16C12 CTL 对可能表达已知 mHAgs 的 EBV-LCL 没有细胞毒性。检测这种 mHAg 的 CTL 可能在 HLA-A31 阳性 BMT 患者的移植物抗白血病(GVL)效应中发挥重要作用。