Voss Ralf-Holger, Kuball Jürgen, Engel Renate, Guillaume Philippe, Romero Pedro, Huber Christoph, Theobald Matthias
Department of Hematology and Oncology, Johannes Gutenberg-University, Mainz, Germany.
Immunol Res. 2006;34(1):67-87. doi: 10.1385/IR:34:1:67.
Retroviral transfer of T cell antigen receptor (TCR) genes selected by circumventing tolerance to broad tumor- and leukemia-associated antigens in human leukocyte antigen (HLA)-A*0201 (A2.1) transgenic (Tg) mice allows the therapeutic reprogramming of human T lymphocytes. Using a human CD8 x A2.1/Kb mouse derived TCR specific for natural peptide-A2.1 (pA2.1) complexes comprising residues 81-88 of the human homolog of the murine double-minute 2 oncoprotein, MDM2(81-88), we found that the heterodimeric CD8 alpha beta coreceptor, but not normally expressed homodimeric CD8 alpha alpha, is required for tetramer binding and functional redirection of TCR- transduced human T cells. CD8+T cells that received a humanized derivative of the MDM2 TCR bound pA2.1 tetramers only in the presence of an anti-human-CD8 anti-body and required more peptide than wild-type (WT) MDM2 TCR+T cells to mount equivalent cytotoxicity. They were, however, sufficiently effective in recognizing malignant targets including fresh leukemia cells. Most efficient expression of transduced TCR in human T lymphocytes was governed by mouse as compared to human constant (C) alphabeta domains, as demonstrated with partially humanized and murinized TCR of primary mouse and human origin, respectively. We further observed a reciprocal relationship between the level of Tg WT mouse relative to natural human TCR expression, resulting in T cells with decreased normal human cell surface TCR. In contrast, natural human TCR display remained unaffected after delivery of the humanized MDM2 TCR. These results provide important insights into the molecular basis of TCR gene therapy of malignant disease.
在人类白细胞抗原(HLA)-A*0201(A2.1)转基因(Tg)小鼠中,通过规避对广泛的肿瘤和白血病相关抗原的耐受性来选择T细胞抗原受体(TCR)基因进行逆转录病毒转移,可实现人类T淋巴细胞的治疗性重编程。使用一种源自人CD8 x A2.1/Kb小鼠的TCR,其对包含鼠双微体2癌蛋白(MDM2)人类同源物第81 - 88位残基的天然肽 - A2.1(pA2.1)复合物具有特异性,我们发现异二聚体CD8αβ共受体而非正常表达的同二聚体CD8αα,是TCR转导的人类T细胞进行四聚体结合和功能重定向所必需的。接受MDM2 TCR人源化衍生物的CD8⁺T细胞仅在存在抗人CD8抗体的情况下结合pA2.1四聚体,并且与野生型(WT)MDM2 TCR⁺T细胞相比,需要更多的肽才能产生同等的细胞毒性。然而,它们在识别包括新鲜白血病细胞在内的恶性靶标方面足够有效。与人类恒定(C)αβ结构域相比,转导的TCR在人类T淋巴细胞中的最有效表达受小鼠结构域调控,分别用源自原代小鼠和人类的部分人源化和鼠源化TCR证明了这一点。我们进一步观察到Tg WT小鼠相对于天然人类TCR表达水平之间的相互关系,导致T细胞表面正常人类TCR水平降低。相反,在递送人源化MDM2 TCR后,天然人类TCR的展示保持不受影响。这些结果为恶性疾病的TCR基因治疗的分子基础提供了重要见解。