Lazarovits A I, Rochon J, Banks L, Hollomby D J, Muirhead N, Jevnikar A M, White M J, Amlot P L, Beauregard-Zollinger L, Stiller C R
Multi-Organ Transplant Service, University Hospital, London, Ontario, Canada.
J Immunol. 1993 Jun 1;150(11):5163-74.
mAb directed against CD7 have been shown to inhibit T cell proliferation in the allogeneic mixed lymphocyte reaction suggesting that CD7 may be an appropriate target for in vivo immunotherapy. We performed a prospective randomized clinical trial with a human-mouse chimeric CD7 mAb (SDZCHH380) and compared it with murine OKT3 for the prophylaxis of kidney transplant rejection. Twenty recipients of first cadaveric renal allografts were randomized to receive either SDZCHH380 or OKT3. SDZCHH380 was well tolerated. Rejection was delayed to day 35. No patients were sensitized to SDZCHH380. In contrast 7/10 OKT3 patients made anti-OKT3 antibodies. SDZCHH380 coated peripheral blood and lymph node T cells and, in contrast to OKT3, induced minimal release of IL-2, IL-6, TNF-alpha, and IFN-gamma. In addition, we showed that CD7-negative T cells mediated rejection in one of the SDZCHH380-treated patients. We conclude that the human-mouse chimeric CD7 mAb SDZCHH380 is well tolerated, is not immunogenic, and merits further study in the prophylaxis of transplant rejection.
已证明针对CD7的单克隆抗体可在同种异体混合淋巴细胞反应中抑制T细胞增殖,这表明CD7可能是体内免疫治疗的合适靶点。我们开展了一项使用人鼠嵌合CD7单克隆抗体(SDZCHH380)的前瞻性随机临床试验,并将其与鼠源性OKT3用于预防肾移植排斥反应的效果进行比较。20例首次接受尸体肾移植的受者被随机分组,分别接受SDZCHH380或OKT3治疗。SDZCHH380耐受性良好。排斥反应延迟至第35天出现。没有患者对SDZCHH380产生致敏反应。相比之下,10例接受OKT3治疗的患者中有7例产生了抗OKT3抗体。SDZCHH380包被外周血和淋巴结T细胞,与OKT3不同的是,它诱导的白细胞介素-2、白细胞介素-6、肿瘤坏死因子-α和干扰素-γ释放极少。此外,我们发现,在1例接受SDZCHH380治疗的患者中,CD7阴性T细胞介导了排斥反应。我们得出结论,人鼠嵌合CD7单克隆抗体SDZCHH380耐受性良好,无免疫原性,在预防移植排斥反应方面值得进一步研究。