Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Pediatric Infectious Diseases and Immunology, Department of Pediatrics, Amalia Children's Hospital, Radboud University Medical Center, Nijmegen, The Netherlands.
J Clin Immunol. 2018 Feb;38(2):185-192. doi: 10.1007/s10875-017-0474-7. Epub 2018 Jan 15.
Antibody replacement therapy for patients with antibody deficiencies contains only IgG. As a result, concurrent IgM and IgA deficiency present in a large proportion of antibody deficient patients persists. Especially patients with IgM deficiency remain at risk for recurrent infections of the gastrointestinal and respiratory tract. The lack of IgM in the current IgG replacement therapy is likely to contribute to the persistence of these mucosal infections because this antibody class is especially important for complement activation on the mucosal surface. We evaluated whether supplementation with IgM increased serum bactericidal capacity in vitro. Serum was collected from a patient with agammaglobulinemia and supplemented with purified serum IgM to normal levels. Antibody and complement deposition on the bacterial surface was determined by multi-color flow cytometry. Bacterial survival in serum was determined by colony-forming unit counts. We present a patient previously diagnosed with agammaglobulinemia due to CD79A (Igα) deficiency revealing a novel pathogenic insertion variant in the CD79a gene (NM_001783.3:c.353_354insT). Despite IgG replacement therapy and antibiotic prophylaxis, this patient developed a Campylobacter jejuni spondylodiscitis of lumbar vertebrae L4-L5. We found that serum IgM significantly contributes to complement activation on the bacterial surface of C. jejuni. Furthermore, supplementation of serum IgM augmented serum bactericidal activity significantly. In conclusion, supplementation of intravenous IgG replacement therapy with IgM may potentially offer greater protection against bacterial infections, also in the context of increasing antibiotic resistance.
抗体缺陷患者的抗体替代疗法仅包含 IgG。因此,在很大一部分抗体缺陷患者中同时存在 IgM 和 IgA 缺陷的情况仍然存在。特别是 IgM 缺陷的患者仍然存在胃肠道和呼吸道反复感染的风险。当前 IgG 替代疗法中缺乏 IgM 可能导致这些黏膜感染持续存在,因为这种抗体类别对于黏膜表面的补体激活尤为重要。我们评估了 IgM 补充是否会增加体外血清杀菌能力。从一名患有丙种球蛋白缺乏症的患者中采集血清,并补充纯化的血清 IgM 以达到正常水平。通过多色流式细胞术测定抗体和补体在细菌表面的沉积。通过菌落形成单位计数确定血清中细菌的存活情况。我们介绍了一名以前因 CD79A(Igα)缺陷而被诊断为丙种球蛋白缺乏症的患者,该患者在 CD79a 基因(NM_001783.3:c.353_354insT)中发现了一种新的致病性插入变异。尽管进行了 IgG 替代疗法和抗生素预防,但该患者仍发生了空肠弯曲菌腰椎 L4-L5 脊椎炎。我们发现血清 IgM 可显著促进空肠弯曲菌表面的补体激活。此外,补充血清 IgM 可显著增强血清杀菌活性。总之,静脉内 IgG 替代疗法中补充 IgM 可能会提供针对细菌感染的更大保护,特别是在抗生素耐药性不断增加的情况下。