Lacuesta Kristine, Buza Elizabeth, Hauser Hans, Granville Laura, Pule Martin, Corboy Greg, Finegold Milton, Weiss Heidi, Chen Si Y, Brenner Malcolm K, Heslop Helen E, Rooney Cliona M, Bollard Catherine M
Center for Cell and Gene Therapy, Baylor College of Medicine, The Methodist Hospital and Texas Children's Hospital, Houston, Texas 77030, USA.
J Immunother. 2006 May-Jun;29(3):250-60. doi: 10.1097/01.cji.0000192104.24583.ca.
Transforming growth factor (TGF)-beta, a pleiotropic cytokine that regulates cell growth, is secreted by many human tumors and markedly inhibits tumor-specific cellular immunity. It has previously been shown by our group that transduction of cytotoxic T lymphocytes (CTLs) with a retroviral vector expressing the dominant-negative TGFbeta type II receptor (DNR) overcomes this tumor evasion in a model of Epstein-Barr virus (EBV)-positive Hodgkin disease. TGFbeta is an important physiologic regulator of T-cell growth and survival, however, abrogation of this regulatory signal in genetically modified cells is potentially problematic. To ensure that unresponsiveness to TGFbeta did not lead to the unregulated growth of genetically modified CTLs, the characteristics of DNR-transduced CTLs in vivo were studied. Donor C57BL6 mice were vaccinated with human papillomavirus-E7 plasmid DNA to induce production of E7-specific CTLs. The E7-specific CTLs were genetically modified to express enhanced green fluorescent protein (GFP) or DNR and administered to syngeneic mice. All mice received monthly boosts with E7 DNA for 9 months, and during this time, transduced CTLs were detected in the peripheral blood of most of the mice using a quantitative real-time polymerase chain reaction. By 12 months, 3 months after cessation of vaccination, no DNR-transduced CTLs or GFP-transduced CTLs were detected in the peripheral blood. There were 4 cases of lymphoma (2 DNR-transduced mice and 2 control mice): all tumors were CD3-/CD8- and were also negative for the DNR transgene. Hence, mature antigen-specific cytotoxic T cells can be genetically modified to resist the antiproliferative effects of TGFbeta without undergoing spontaneous lymphoproliferation in vivo. They may be of value for treating human cancers, which use TGFbeta as a powerful immune evasion mechanism.
转化生长因子(TGF)-β是一种调节细胞生长的多效性细胞因子,由许多人类肿瘤分泌,并显著抑制肿瘤特异性细胞免疫。我们小组之前已经证明,用表达显性负性TGFβ II型受体(DNR)的逆转录病毒载体转导细胞毒性T淋巴细胞(CTL),可在爱泼斯坦-巴尔病毒(EBV)阳性霍奇金病模型中克服这种肿瘤逃逸现象。然而,TGFβ是T细胞生长和存活的重要生理调节因子,在基因修饰细胞中消除这种调节信号可能存在问题。为确保对TGFβ无反应不会导致基因修饰的CTL不受控制地生长,研究了体内DNR转导的CTL的特性。给供体C57BL6小鼠接种人乳头瘤病毒-E7质粒DNA,以诱导产生E7特异性CTL。将E7特异性CTL进行基因修饰以表达增强型绿色荧光蛋白(GFP)或DNR,并给予同基因小鼠。所有小鼠每月用E7 DNA加强免疫9个月,在此期间,使用定量实时聚合酶链反应在大多数小鼠的外周血中检测到转导的CTL。到12个月时,即停止接种疫苗3个月后,在外周血中未检测到DNR转导的CTL或GFP转导的CTL。有4例淋巴瘤(2只DNR转导小鼠和2只对照小鼠):所有肿瘤均为CD3-/CD8-,且DNR转基因也为阴性。因此,成熟的抗原特异性细胞毒性T细胞可以进行基因修饰,以抵抗TGFβ的抗增殖作用,而不会在体内发生自发的淋巴细胞增殖。它们可能对治疗将TGFβ作为强大免疫逃逸机制的人类癌症有价值。