Nocera Arcangelo
Unità Operativa Semplice Immunologia dei Trapianti, Dipartimento Trapianti, Padiglione XIII II piano, Azienda Ospedaliera Universitaria S. Martino, Genova.
G Ital Nefrol. 2009 Jul-Aug;26(4):499-515.
It is well known that the presence of alloantibodies against human HLA class I (A, B, C) and class II (DR, DQ) antigens in transplant recipients waiting for a first or subsequent kidney transplant has a significant negative impact on graft outcome, with increased acute and chronic rejection rates. HLA antibodies, present in hyperimmunized patients (PRA > 80%) as a result of pregnancies, blood transfusions and previous failed grafts, once thought to be a formidable barrier to renal transplantation, can now be overcome with excellent results by means of desensitization protocols in kidney transplant recipients from living or cadaver donors. Such pretransplant desensitization protocols consist of high-dose intravenous immunoglobulin infusions (IVIg-HD), plasmapheresis associated with low-dose IVIg (IVIg-LD) and immunoabsorption by protein-A sepharose or Ig-sepharose columns. All of the above treatments, associated in many cases with the anti-CD20 monoclonal antibody Rituximab, have been widely applied in living donor kidney transplant recipients showing donor-specific anti-HLA antibodies. Similar desensitization protocols have been used for non-A2 AB0-incompatible living donor kidney transplants. These techniques have allowed successful transplantation in this high-risk patient category by providing live donor kidneys that function promptly with minimal risk of early loss, and have consequently increased the organ donor pool. Long-term follow- up of these patients and the application on a wider scale of these techniques, which for many patients may represent the only realistic chance of a successful transplant, will provide the definitive answers about their real efficacy.
众所周知,在等待首次或再次肾移植的受者体内,针对人类HLA I类(A、B、C)和II类(DR、DQ)抗原的同种抗体的存在对移植结果有显著负面影响,急性和慢性排斥反应率会增加。由于妊娠、输血和既往移植失败,高敏患者(PRA>80%)体内存在HLA抗体,这些抗体曾被认为是肾移植的巨大障碍,但现在通过对活体或尸体供肾的肾移植受者采用脱敏方案,可以取得很好的效果来克服这一障碍。这种移植前脱敏方案包括大剂量静脉注射免疫球蛋白(IVIg-HD)、与小剂量IVIg联合的血浆置换(IVIg-LD)以及通过蛋白A琼脂糖或Ig琼脂糖柱进行免疫吸附。上述所有治疗方法,在许多情况下与抗CD20单克隆抗体利妥昔单抗联合使用,已广泛应用于显示供体特异性抗HLA抗体的活体供肾移植受者。类似的脱敏方案也用于非A2 ABO血型不相容的活体供肾移植。这些技术通过提供能迅速发挥功能且早期丢失风险最小的活体供肾,使这类高风险患者成功进行了移植,从而增加了器官供体库。对这些患者的长期随访以及这些技术在更广泛范围内的应用,对许多患者来说可能是成功移植的唯一现实机会,将为其实际疗效提供明确答案。