Warren E H, Greenberg P D, Riddell S R
Fred Hutchinson Cancer Research Center, Seattle, WA 98104, USA.
Blood. 1998 Mar 15;91(6):2197-207.
Cytotoxic T lymphocytes (CTL) specific for human minor histocompatibility (H) antigens can be isolated from the blood of major histocompatibility complex (MHC)-matched allogeneic bone marrow transplant (BMT) recipients and may play a prominent role in the graft-versus-host (GVH) and graft-versus-leukemia (GVL) reactions (Tsoi et al, J Immunol 125:2258, 1980; Tsoi et al, Transplant Proc 15:1484, 1983; Goulmy et al, Nature 302:159, 1983; Irle et al, Transplantation 40:329, 1985; and Niederwieser et al, Blood 81:2200, 1993). The identification of minor H antigens that are expressed in hematopoietic cells, including leukemic cells, but not in fibroblasts and other tissue types has suggested that such tissue-restricted antigens could potentially serve as targets for T-cell immunotherapy to enhance GVL activity without inducing GVH disease (de Bueger et al, J Immunol 149:1788, 1992; van der Harst et al, Blood 83:1060, 1994; and Dolstra et al, J Immunol 158:560, 1997). To explore the feasibility of this strategy, donor CD3+CD8+ CTL clones specific for recipient minor H antigens were isolated and characterized from allogeneic BMT recipients. CTL clones were obtained from the majority of donor/recipient pairs. Seventeen distinct minor H antigens distinguishable by their MHC-restricting allele, population frequency, and/or distribution of tissue expression were defined by 56 CD3+CD8+ CTL clones isolated from these patients. The MHC-restricting alleles for these CTL clones included HLA-A2 and HLA-B7, which had previously been shown to present minor H antigens to CTL, as well as HLA-A3, -A11, -B8, -B53, and -Cw7, which had not previously been described to present minor H antigens to CTL. Estimated phenotype frequencies for these 17 distinct minor H antigens range from 0.17 to 0.92. In vitro cytotoxicity assays using hematopoietic cells and fibroblasts as target cells showed that 5 of the 17 minor H antigens were expressed in both hematopoietic cells and fibroblasts. However, 12 were presented for CTL recognition only by hematopoietic cells and not by dermal fibroblasts derived from the same donors. These results significantly extend the spectrum of CTL-defined human minor H antigens that could potentially serve as target antigens for cellular immunotherapy to promote GVL activity after allogeneic BMT.
针对人类次要组织相容性(H)抗原的细胞毒性T淋巴细胞(CTL)可从主要组织相容性复合体(MHC)匹配的异基因骨髓移植(BMT)受者的血液中分离出来,并且可能在移植物抗宿主(GVH)和移植物抗白血病(GVL)反应中发挥重要作用(Tsoi等人,《免疫学杂志》125:2258,1980;Tsoi等人,《移植会议录》15:1484,1983;Goulmy等人,《自然》302:159,1983;Irle等人,《移植》40:329,1985;以及Niederwieser等人,《血液》81:2200,1993)。在造血细胞(包括白血病细胞)中表达但在成纤维细胞和其他组织类型中不表达的次要H抗原的鉴定表明,这种组织限制性抗原可能潜在地作为T细胞免疫治疗的靶点,以增强GVL活性而不诱发GVH疾病(de Bueger等人,《免疫学杂志》149:1788,1992;van der Harst等人,《血液》83:1060,1994;以及Dolstra等人,《免疫学杂志》158:560,1997)。为了探索该策略的可行性,从异基因BMT受者中分离并鉴定了针对受者次要H抗原的供体CD3+CD8+ CTL克隆。大多数供体/受者对都获得了CTL克隆。从这些患者中分离出的56个CD3+CD8+ CTL克隆定义了17种不同的次要H抗原,这些抗原可通过其MHC限制性等位基因、群体频率和/或组织表达分布来区分。这些CTL克隆的MHC限制性等位基因包括先前已被证明可将次要H抗原呈递给CTL的HLA - A2和HLA - B7,以及先前未被描述可将次要H抗原呈递给CTL的HLA - A3、- A11、- B8、- B53和- Cw7。这17种不同次要H抗原的估计表型频率范围为0.17至0.92。使用造血细胞和成纤维细胞作为靶细胞的体外细胞毒性试验表明,17种次要H抗原中有5种在造血细胞和成纤维细胞中均有表达。然而,其中12种仅由造血细胞呈递给CTL识别,而来自相同供体的皮肤成纤维细胞则不能呈递。这些结果显著扩展了CTL定义的人类次要H抗原的范围,这些抗原可能潜在地作为细胞免疫治疗的靶抗原,以促进异基因BMT后的GVL活性。