Goldfarb N S, Avery R K, Goormastic M, Mehta A C, Schilz R, Smedira N, Pien L, Haug M T, Gordon S M, Hague L K, Dresing J M, Evans-Walker T, Maurer J R
Transplant Center and Department of Pulmonary Medicine, Cleveland Clinic Foundation, OH 44195, USA.
Transplantation. 2001 Jan 27;71(2):242-6. doi: 10.1097/00007890-200101270-00013.
Infectious complications continue to represent a significant source of morbidity and mortality in lung transplant recipients. Identifying specific, remediable immune defects is of potential value. After one lung transplant patient with recurrent infections was noted to be severely hypogammaglobulinemic, a screening program for humoral immune defects was instituted. The objectives were to define the prevalence of hypogammaglobulinemia in lung transplant recipients, assess levels of antibody to specific pathogens, and correlate infectious disease outcomes and survival with immunoglobulin levels.
All lung transplant recipients followed at a single center between October 1996 and June 1999 underwent a posttransplant humoral immune status survey as part of routine posttransplant follow-up. This survey consists of total immunoglobulin levels (IgG, IgM, IgA), IgG subclasses (IgG1-4), and antibody titers to Pneumococcus, diphtheria, and tetanus. Since February 1997, this survey has been incorporated into the pretransplant evaluation as well. Humoral survey results for October 1996 through July 1999 were recorded, and clinical information on major infectious disease outcomes was obtained from chart reviews, discharge summaries, the Cleveland Clinic Unified Transplant Database, and review of all microbiological studies and pathology results for each patient.
Of 67 patients with humoral immune surveys drawn posttransplant, 47 (70%) had IgG levels less than 600 mg/dl (normal 717-1410 mg/dl), of which 25 (37%) had IgG levels less than 400 mg/dl ("lowest IgG group") and 22 (33%) had IgG levels between 400 and 600 mg/dl ("moderately low IgG group"). A total of 20 patients (30%) had IgG levels of more than 600 mg/dl ("normal IgG group"). Infections that were significantly more common in the lowest IgG group, and more common in the moderately low IgG group than the normal IgG group, included: number of pneumonias (P=0.0006), bacteremias (P=0.02), total bacterial infections (P=0.002), tissue-invasive cytomegalovirus (P=0.01), invasive aspergillosis (P=0.001), total fungal infections (P=0.001), and total infections (P=0.006). Median hospital days per posttransplant year was significantly different in the three groups (11.0 vs. 7.4 vs. 2.8 days, P=0.0003.) Invasive aspergillosis occurred in 44% of the lowest IgG group, 9% of the moderately low IgG group, and 0% of the normal IgG group (P<0.001). Survival was poorest in the lowest IgG group and intermediate in the moderately low IgG group. IgG subclass deficiencies occurred in a variety of patterns. Hypogammaglobulinemic patients lacked protective responses to Pneumococcus in 14/47 (30%), diphtheria in 15%, and tetanus in 19%. In a group of 48 patients screened pretransplant, 90% had normal immunoglobulin levels.
Hypogammaglobulinemia in lung transplant recipients is more common than has been previously recognized. An IgG level of less than 400 mg/dl identifies a group at extremely high risk of bacterial and fungal infections, tissue-invasive cytomegalovirus, and poorer survival. Immunoglobulin monitoring may offer an opportunity for intensive surveillance, tapering of immunosuppression, and preemptive therapy for infection.
感染性并发症仍是肺移植受者发病和死亡的重要原因。识别特定的、可纠正的免疫缺陷具有潜在价值。在一名肺移植患者反复感染且被发现严重低丙种球蛋白血症后,启动了一项体液免疫缺陷筛查计划。目的是确定肺移植受者中低丙种球蛋白血症的患病率,评估针对特定病原体的抗体水平,并将感染性疾病结局和生存率与免疫球蛋白水平相关联。
1996年10月至1999年6月在单一中心随访的所有肺移植受者,作为移植后常规随访的一部分,接受了移植后体液免疫状态调查。该调查包括总免疫球蛋白水平(IgG、IgM、IgA)、IgG亚类(IgG1 - 4)以及针对肺炎球菌、白喉和破伤风的抗体滴度。自1997年2月起,该调查也被纳入移植前评估。记录了1996年10月至1999年7月的体液调查结果,并从病历审查、出院小结、克利夫兰诊所统一移植数据库以及每位患者的所有微生物学研究和病理结果审查中获取了主要感染性疾病结局的临床信息。
在67例移植后进行体液免疫调查的患者中,47例(70%)的IgG水平低于600mg/dl(正常为717 - 1410mg/dl),其中25例(37%)的IgG水平低于400mg/dl(“最低IgG组”),22例(33%)的IgG水平在400至600mg/dl之间(“中度低IgG组”)。共有20例患者(30%)的IgG水平高于600mg/dl(“正常IgG组”)。最低IgG组中明显更常见、且中度低IgG组比正常IgG组更常见的感染包括:肺炎数量(P = 0.0006)、菌血症(P = 0.02)、总细菌感染(P = 0.002)、组织侵袭性巨细胞病毒感染(P = 0.01)、侵袭性曲霉病(P = 0.001)、总真菌感染(P = 0.001)以及总感染(P = 0.006)。三组中移植后每年的中位住院天数有显著差异(11.0天对7.4天对2.8天,P = 0.0003)。侵袭性曲霉病在最低IgG组中的发生率为44%,中度低IgG组为9%,正常IgG组为0%(P < 0.001)。最低IgG组的生存率最差,中度低IgG组居中。IgG亚类缺陷以多种模式出现。低丙种球蛋白血症患者中,14/47(30%)对肺炎球菌缺乏保护性反应,15%对白喉缺乏,19%对破伤风缺乏。在一组48例移植前筛查的患者中,90%的免疫球蛋白水平正常。
肺移植受者中的低丙种球蛋白血症比以前认识到的更为常见。IgG水平低于400mg/dl确定了一组发生细菌和真菌感染、组织侵袭性巨细胞病毒感染风险极高且生存率较差的人群。免疫球蛋白监测可能为强化监测以及调整免疫抑制和感染的抢先治疗提供机会。