Najafian Nader, Salama Alan D, Fedoseyeva Eugenia V, Benichou Gilles, Sayegh Mohamed H
*Laboratory of Immunogenetics and Transplantation, Brigham and Women's Hospital, Nephrology Division, Children's Hospital, Harvard Medical School, Boston, Massachusetts, and Cellular and Molecular Immunology Laboratory, Schepens Eye Research Institute, and Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts.
J Am Soc Nephrol. 2002 Jan;13(1):252-259. doi: 10.1681/ASN.V131252.
Chronic allograft dysfunction, which is the most common cause of late allograft failure, is in part caused by an ongoing immune response orchestrated by T lymphocytes primed by the indirect pathway of allorecognition. The low frequencies of such T cells have made it difficult to study indirect alloreactivity by using currently available assays. The development of a sensitive, clinically useful method of measuring indirect alloreactivity among human renal transplant recipients was thus attempted. Furthermore, in a pilot immunologic study, the contribution of the indirect pathway was studied in two groups of renal transplant recipients, i.e., patients with no prior acute rejection episodes and stable renal function ("stable" patients) and patients with at least one previous episode of biopsy-proven acute rejection, who were thus at risk for the development of chronic rejection ("high-risk" patients). The frequencies of type 1 T helper (interferon-gamma-producing) and type 2 T helper (interleukin-5- and -10-producing) peripheral blood lymphocytes reactive with a panel of synthetic peptides (corresponding to sequences from donor HLA-DR molecules) were determined for renal transplant recipients and normal control subjects by using an enzyme-linked immunosorbent spot assay (ELISPOT). Among recipients of DR-mismatched allografts, a cut-off value of 60 interferon-gamma spots/10(6) cells significantly (P = 0.02) separated stable patients (creatinine concentration, 1.1 +/- 0.3 mg/dl) from high-risk patients (creatinine concentration, 2.3 +/- 1.7 mg/dl). This is the first demonstration that the enzyme-linked immunosorbent spot assay can be used to monitor indirect alloreactivity to donor HLA-DR peptides among renal transplant recipients. These data provide the rationale for the prospective study of indirect alloreactivity among transplant recipients, to allow predictions of which patients would be at risk for the development of chronic rejection and thus allow appropriate planning of future interventions.
慢性移植肾失功是移植肾晚期失功的最常见原因,部分是由间接途径同种异体识别启动的T淋巴细胞所协调的持续免疫反应引起的。这类T细胞频率较低,使得利用现有检测方法研究间接同种异体反应性变得困难。因此,人们尝试开发一种灵敏且临床实用的方法来测量人类肾移植受者的间接同种异体反应性。此外,在一项初步免疫学研究中,对两组肾移植受者进行了间接途径作用的研究,即既往无急性排斥发作且肾功能稳定的患者(“稳定”患者)和至少有一次经活检证实的急性排斥发作且因此有发生慢性排斥风险的患者(“高危”患者)。通过酶联免疫斑点试验(ELISPOT)测定了肾移植受者和正常对照受试者外周血中与一组合成肽(对应供体HLA - DR分子序列)反应的1型辅助性T细胞(产生干扰素 - γ)和2型辅助性T细胞(产生白细胞介素 - 5和 - 10)的频率。在接受DR错配移植肾的受者中,以60个干扰素 - γ斑点/10⁶细胞为临界值,可显著(P = 0.02)区分稳定患者(肌酐浓度,1.1±0.3mg/dl)和高危患者(肌酐浓度,2.3±1.7mg/dl)。这是首次证明酶联免疫斑点试验可用于监测肾移植受者对供体HLA - DR肽的间接同种异体反应性。这些数据为前瞻性研究移植受者的间接同种异体反应性提供了理论依据,以便预测哪些患者有发生慢性排斥的风险,从而为未来干预措施的合理规划提供依据。