David Geffen School of Medicine, University of California, Los Angeles, California.
David Geffen School of Medicine, University of California, Los Angeles, California; Division of Hematology-Oncology, Department of Medicine, Ronald Reagan UCLA Medical Center, Los Angeles, California.
Biol Blood Marrow Transplant. 2018 Aug;24(8):1715-1720. doi: 10.1016/j.bbmt.2018.03.010. Epub 2018 Mar 16.
Nocardial infections have been rare after allogeneic hematopoietic stem cell transplantation (HSCT). We report 10 recent cases of late-onset nocardiosis (median time of onset of 508 days after transplantation) primarily in patients on high doses of corticosteroids for graft-versus-host disease. All 10 patients had pulmonary infection caused by Nocardia species susceptible to trimethoprim-sulfamethoxazole (TMP-SMX). At time of diagnosis 8 of 10 patients were not receiving TMP-SMX for prophylaxis of Pneumocystis jiroveci pneumonia (PJP; 7 on atovaquone, 1 on i.v. pentamidine). After the initiation of atovaquone prophylaxis for PJP in place of TMP-SMX for many UCLA allogeneic HSCT patients in 2012, 9 cases of nocardiosis occurred in 411 patients (2.2%) over the next 6 years (2012 to 2017) compared with only 1 case in 575 patients (0.17%) during the previous 12 years (2000 to 2011). Although there were no deaths directly related to nocardial infection treated primarily with TMP-SMX, overall mortality in this group of patients was 40%. Based on this experience, the use of atovaquone for PJP prophylaxis in place of TMP-SMX may be associated with an increased risk for previously rare nocardial infections after allogeneic HSCT.
异基因造血干细胞移植(HSCT)后诺卡氏菌感染较为罕见。我们报告了 10 例近期发生的迟发性诺卡氏菌病(移植后中位发病时间为 508 天),主要发生在因移植物抗宿主病而接受大剂量皮质类固醇治疗的患者中。所有 10 例患者均患有对复方磺胺甲噁唑(TMP-SMX)敏感的诺卡氏菌属肺部感染。诊断时,10 例患者中有 8 例未接受 TMP-SMX 预防肺孢子菌肺炎(PJP;7 例使用阿托伐醌,1 例使用静脉注射戊烷脒)。2012 年,在加利福尼亚大学洛杉矶分校的许多异基因 HSCT 患者中,TMP-SMX 被阿托伐醌取代用于预防 PJP 后,随后的 6 年(2012 年至 2017 年)中,411 例患者中有 9 例(2.2%)发生了诺卡氏菌病,而在之前的 12 年(2000 年至 2011 年)中,575 例患者中仅有 1 例(0.17%)。尽管没有直接因主要使用 TMP-SMX 治疗而死于诺卡氏菌感染的病例,但该组患者的总死亡率为 40%。根据这一经验,用阿托伐醌替代 TMP-SMX 预防 PJP 可能会增加异基因 HSCT 后罕见的诺卡氏菌感染的风险。