Institute of Clinical Medicine, University of Tromsø, Bone and joint research group, Tromsø, Norway,
Clin Rheumatol. 2013 Nov;32(11):1677-81. doi: 10.1007/s10067-013-2293-4. Epub 2013 Jun 11.
Reports in haematology, transplantation medicine and rheumatology indicate that Rituximab, a B cell depleting therapy, increases the risk for Pneumocystis jiroveci pneumopathy. Patients with antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis have an increased incidence of P. jiroveci pneumopathy compared to other autoimmune diseases and Rituximab is often used to induce and maintain remission. Herein, we present a case of a patient with granulomatosis with polyangiitis treated with Rituximab for relapse that developed P. jiroveci pneumopathy 3 months after and we review the relevant literature to assess P. jiroveci pneumopathy incidence and risks factors under Rituximab. We also discuss whether P. jiroveci screening before Rituximab and P. jiroveci pneumopathy prophylaxis under Rituximab are indicated. P. jiroveci colonisation is found in 25 % of patients with autoimmune diseases. However, the association between colonisation and P. jiroveci pneumopathy development is not very strong. P. jiroveci pneumopathy incidence in ANCA-associated vasculitis patients treated with Rituximab is found to be 1.2 %. Therefore, evidence and practice do not support the use of P. jiroveci pneumopathy chemoprophylaxis in all ANCA-associated vasculitis patients receiving Rituximab. CD4 cell count cut-off does not work well in patients treated with Rituximab as it does not reflect T cell impairment following B cell depletion. To help stratify the risk of both colonisation and P. jiroveci pneumopathy development, assessment of the patient's net state of immunodeficiency before administering Rituximab-including age, renal or lung involvement, previous infections due to T cell dysfunction, blood tests (lymphocytopenia, low CD4 cell count) and concomitant therapy-is warranted.
血液学、移植医学和风湿病学的报告表明,利妥昔单抗(一种 B 细胞耗竭疗法)会增加卡氏肺孢子菌肺炎的风险。与其他自身免疫性疾病相比,抗中性粒细胞胞质抗体(ANCA)相关血管炎患者发生卡氏肺孢子菌肺炎的发病率更高,而利妥昔单抗常用于诱导和维持缓解。在此,我们报告了一例复发性肉芽肿伴多血管炎患者,在接受利妥昔单抗治疗后 3 个月发生卡氏肺孢子菌肺炎的病例,并回顾了相关文献,以评估利妥昔单抗下卡氏肺孢子菌肺炎的发病率和危险因素。我们还讨论了在利妥昔单抗治疗前是否需要进行卡氏肺孢子菌筛查以及在利妥昔单抗治疗下是否需要预防性使用卡氏肺孢子菌肺炎。25%的自身免疫性疾病患者存在卡氏肺孢子菌定植。然而,定植与卡氏肺孢子菌肺炎发展之间的关联并不十分强烈。在接受利妥昔单抗治疗的 ANCA 相关血管炎患者中,卡氏肺孢子菌肺炎的发病率为 1.2%。因此,证据和实践并不支持在所有接受利妥昔单抗治疗的 ANCA 相关血管炎患者中预防性使用卡氏肺孢子菌肺炎化学预防。CD4 细胞计数截止值在接受利妥昔单抗治疗的患者中效果不佳,因为它不能反映 B 细胞耗竭后 T 细胞功能障碍。为了帮助分层评估患者在接受利妥昔单抗治疗前的免疫缺陷状况(包括年龄、肾脏或肺部受累、因 T 细胞功能障碍而导致的既往感染、血液检查[淋巴细胞减少、低 CD4 细胞计数]和同时进行的治疗),以评估定植和卡氏肺孢子菌肺炎发展的风险。