利妥昔单抗治疗多发性硬化症患者的低γ球蛋白血症和感染。

IF 7.5
Marine Perriguey, Adil Maarouf, Jan-Patrick Stellmann, Audrey Rico, Clemence Boutiere, Sarah Demortiere, Pierre Durozard, Jean Pelletier, Bertrand Audoin
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引用次数: 25

摘要

背景和目的:确定接受利妥昔单抗(RTX)治疗的多发性硬化症(PwMS)患者低γ球蛋白血症和感染的频率。方法:这项前瞻性观察研究包括2015年至2020年期间在法国马赛大学医院接受RTX的所有连续PwMS。患者就诊至少每6个月一次。结果:我们纳入188例患者(151例复发缓解型MS;平均年龄43.4岁[SD 12.9],中位病程10年[范围0-36],中位扩展残疾状态量表5年[范围0-8],中位随访3.5年[范围1-5.8],中位RTX输注次数5年[范围1-9])。总体而言,188例患者中133例(70.7%)出现症状性感染317例,188例患者中11例(5.9%)出现严重感染13例。4年后,24.4%的患者(95% CI 18.0-33.1)无任何感染,92.0% (95% CI 87.1-97.1)未发生严重感染。在RTX发病时,188例患者中有32例(17%)免疫球蛋白G (IgG)水平异常。RTX后IgG水平p = 0.03)。IgG水平降低的风险p = 0.01)。讨论:在接受RTX治疗的PwMS中,IgG水平降低是常见的,并且与感染的风险相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hypogammaglobulinemia and Infections in Patients With Multiple Sclerosis Treated With Rituximab.

Hypogammaglobulinemia and Infections in Patients With Multiple Sclerosis Treated With Rituximab.

Hypogammaglobulinemia and Infections in Patients With Multiple Sclerosis Treated With Rituximab.

Hypogammaglobulinemia and Infections in Patients With Multiple Sclerosis Treated With Rituximab.

Background and objectives: To determine the frequency of hypogammaglobulinemia and infections in patients with multiple sclerosis (PwMS) receiving rituximab (RTX).

Methods: This prospective observational study included all consecutive PwMS receiving RTX at the university hospital of Marseille, France, between 2015 and 2020. Patient visits occurred at least every 6 months.

Results: We included 188 patients (151 with relapsing-remitting MS; the mean age was 43.4 years [SD 12.9], median disease duration 10 years [range 0-36], median Expanded Disability Status Scale 5 [range 0-8], median follow-up 3.5 years [range 1-5.8], and median number of RTX infusions 5 [range 1-9]). Overall, 317 symptomatic infections and 13 severe infections occurred in 133 of 188 (70.7%) and 11 of 188 (5.9%) patients, respectively. After 4 years, 24.4% of patients (95% CI 18.0-33.1) were free of any infection and 92.0% (95% CI 87.1-97.1) had not experienced a severe infection. At RTX onset, the immunoglobulin G (IgG) level was abnormal in 32 of 188 (17%) patients. After RTX, IgG level was <7, <6, <4 and <2 g/L for 83 (44%), 44 (23.4%), 8 (4.2%) and 1 (0.53%) patients, respectively. The risk of infection was associated with reduced IgG levels (multivariate Cox proportional hazards hazard ratio [HR] = 0.86, 95% CI 0.75-0.98, p = 0.03). The risk of reduced IgG level <6 g/L increased with age (HR = 1.36, 95% CI 1.05-1.75, p = 0.01).

Discussion: In PwMS receiving RTX, reduced IgG level was frequent and interacted with the risk of infection.

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