Necker-Pasteur Center for Infectious Diseases and Tropical Medicine, Necker-Enfants Malades University Hospital, Assistance Publique des Hôpitaux de Paris (AP-HP), Université de Paris, 149 Rue de Sèvres, 75015, Paris, France.
Pediatric Immuno-Hematology and Rheumatology Unit, Necker-Enfants Malades University Hospital, AP-HP, Université de Paris, Paris, France.
J Clin Immunol. 2021 Aug;41(6):1266-1271. doi: 10.1007/s10875-021-01043-1. Epub 2021 Apr 21.
Outcome of patients with X-linked agammaglobulinemia (XLA) has improved with the widespread use of immunoglobulin replacement therapy (IgRT). There are few data on the spectrum of infections experienced by patients undergoing IgRT. We carried out a retrospective cross-sectional analysis of the records of XLA patients seen at Necker-Enfants Malades Hospital, Paris. For each infection, we evaluated infection site, microbial etiology, antibiotic prophylaxis, immunosuppressive treatment, IgRT route, and last known IgG trough level. Sixty patients were included, who cumulated a follow-up of 1470 patient-years. We recorded 188 infections, including 97 after initiation of IgRT. The rate of infection was highest before IgRT (0.66 vs. 0.06 per person-year (ppy), p < 0.001) and was higher after the age of 16 compared to before (0.14 vs. 0.05 ppy, p = 0.048). It was similar for patients receiving intravenous or subcutaneous Ig (0.09 vs 0.05 ppy, p = 0.54). The lungs and gastrointestinal tract accounted for 71% of infection sites. Forty-six (47%) infections occurred in patients receiving antibiotic prophylaxis. Sixteen (16.5%) infections occurred in patients receiving immunosuppressive therapy, which more frequently occurred after age 16 (35% vs. 2.4%, p < 0.001). The median IgG trough level prior to all infections was 8.4 g/L. Almost half (44.3%) of infections occurred with prior IgG trough levels > 8 g/L, and 16/97 (16.7%) in patients with trough levels > 10 g/L. Infection remains a significant issue in patients with XLA undergoing IgRT despite adequate IgG trough levels. Chronic inflammatory manifestations of X-linked agammaglobulinemia and immunosuppressive therapies may be significant drivers of infection during adulthood.
接受免疫球蛋白替代疗法 (IgRT) 的 X 连锁无丙种球蛋白血症 (XLA) 患者的预后已得到改善。关于接受 IgRT 的患者所经历的感染谱的数据很少。我们对巴黎 Necker-Enfants Malades 医院就诊的 XLA 患者的记录进行了回顾性横断面分析。对于每种感染,我们评估了感染部位、微生物病因、抗生素预防、免疫抑制治疗、IgRT 途径和最后一次已知 IgG 谷值水平。共纳入 60 例患者,累计随访 1470 患者年。我们记录了 188 例感染,其中 97 例发生在开始 IgRT 之后。在 IgRT 之前感染率最高(0.66 比 0.06 人年,p<0.001),16 岁后高于 16 岁前(0.14 比 0.05 人年,p=0.048)。静脉内或皮下 Ig 治疗的患者感染率相似(0.09 比 0.05 人年,p=0.54)。肺部和胃肠道占感染部位的 71%。46(47%)例感染发生在接受抗生素预防的患者中。16(16.5%)例感染发生在接受免疫抑制治疗的患者中,16 岁后更常发生(35%比 2.4%,p<0.001)。所有感染前的 IgG 谷值中位数为 8.4g/L。近一半(44.3%)的感染发生在 IgG 谷值水平>8g/L 之前,而 97 例感染中有 16 例(16.7%)的 IgG 谷值水平>10g/L。尽管 IgG 谷值水平充足,但 XLA 患者接受 IgRT 后感染仍然是一个重要问题。X 连锁无丙种球蛋白血症的慢性炎症表现和免疫抑制治疗可能是成年期感染的重要驱动因素。