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首页> 外文期刊>Journal of Clinical Immunology >Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study.
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Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study.

机译:免疫球蛋白替代疗法对原发性抗体缺乏症患者临床结局的有效性:一项多中心前瞻性队列研究的结果。

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摘要

A 5-years multicenter prospective study on 201 patients with common variable immunodeficiencies and 101 patients with X-linked agammaglobulinemia over a cumulative follow-up period of 1,365 patient-years was conducted to identify prognostic markers and risk factors for associated clinical co-morbidities, the effects of long-term immunoglobulin treatment and the IgG trough level to be maintained over time required to minimise infection risk. Overall, 21% of the patients with common variable immunodeficiencies and 24% of patients with X-linked agammaglobulinemia remained infection free during the study. A reduction of pneumonia episodes has been observed after initiation of Ig replacement. During the observation time, pneumonia incidence remained low and constant over time. Patients with pneumonia did not have significant lower IgG trough levels than patients without pneumonia, with the exception of patients whose IgG trough levels were persistently <400 mg/dL. In X-linked agammaglobulinemia, the only co-morbidity risk factor identified for pneumonia by the final multivariable model was the presence of bronchiectasis. In common variable immunodeficiencies, our data allowed us to identify a clinical phenotype characterised by a high pneumonia risk: patients with low IgG and IgA levels at diagnosis; patients who had IgA level <7 mg/dL and who had bronchiectasis. The effect of therapy with immunoglobulins at replacement dosage for non-infectious co-morbidities (autoimmunity, lymphocytic hyperplasia and enteropathy) remains to be established. A unique general protective trough IgG level in antibody deficiency patients will remain undefined because of the major role played by the progression of lung disease in X-linked agammaglobulinemia and in a subset of patients with common variable immunodeficiencies.
机译:一项为期5年的多中心前瞻性研究,在1,365个患者-年的累积随访期内,对201名具有共同可变免疫缺陷的患者和101例X连锁性丙种球蛋白血症的患者进行了研究,以确定相关临床合并症的预后指标和危险因素,长期免疫球蛋白治疗的效果以及IgG谷水平应随时间而保持,以最大程度地降低感染风险。总体而言,在研究过程中,有21%的具有共同可变免疫缺陷的患者和24%的X连锁性丙种球蛋白血症的患者保持无感染。开始更换Ig后,肺炎发作减少。在观察期间,肺炎的发生率一直保持较低水平,并且随时间推移保持恒定。肺炎患者的IgG谷值水平没有非肺炎患者,但IgG谷值持续<400 mg / dL的患者除外。在X连锁的丙种球蛋白血症中,由最终的多变量模型确定的肺炎的唯一合并症危险因素是支气管扩张。在常见的可变免疫缺陷中,我们的数据使我们能够确定以高肺炎风险为特征的临床表型:诊断时IgG和IgA水平低的患者; IgA水平<7 mg / dL且患有支气管扩张的患者。补充免疫球蛋白治疗非感染性合并症(自身免疫,淋巴细胞增生和肠病)的效果尚待确定。由于X连锁的丙种球蛋白血症和部分具有可变免疫缺陷的患者中肺部疾病的进展起着重要作用,因此抗体缺乏症患者中独特的一般性保护槽IgG水平仍然不确定。

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