Brownlie Helen, Speight Nigel
Independent Researcher and Former Local Government Officer, Social Policy and Research, Glasgow G2 4P, UK.
Paediatrician and Independent Researcher, Durham DH1 1QN, UK.
Healthcare (Basel). 2021 Nov 12;9(11):1546. doi: 10.3390/healthcare9111546.
The findings of controlled trials on use of intravenous immunoglobulin G (IV IgG) to treat myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are generally viewed as representing mixed results. On detailed review, a clearer picture emerges, which suggests that the potential therapeutic value of this intervention has been underestimated. Our analysis is consistent with the propositions that: (1) IgG is highly effective for a proportion of patients with severe and well-characterised ME/CFS; (2) responders can be predicted with a high degree of accuracy based on markers of immune dysfunction. Rigorous steps were taken in the research trials to record adverse events, with transient symptom exacerbation commonly experienced in both intervention and placebo control groups, suggesting that this reflected the impact of participation on people with an illness characterised by post-exertional symptom exacerbation. Worsening of certain specific symptoms, notably headache, did occur more commonly with IgG and may have been concomitant to effective treatment, being associated with clinical improvement. The findings emerging from this review are supported by clinical observations relating to treatment of patients with severe and very severe ME/CFS, for whom intramuscular and subcutaneous administration provide alternative options. We conclude that: (1) there is a strong case for this area of research to be revived; (2) pending further research, clinicians would be justified in offering a course of IgG to selected ME/CFS patients at the more severe end of the spectrum. As the majority of trial participants had experienced an acute viral or viral-like onset, we further suggest that IgG treatment may be pertinent to the care of some patients who remain ill following infection with SARS-CoV-2 virus.
关于使用静脉注射免疫球蛋白G(IV IgG)治疗肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)的对照试验结果,总体上被认为是喜忧参半。经过详细审查,情况变得更加清晰,这表明这种干预措施的潜在治疗价值被低估了。我们的分析与以下观点一致:(1)IgG对一部分症状严重且特征明确的ME/CFS患者非常有效;(2)基于免疫功能障碍标志物,可以高度准确地预测反应者。研究试验中采取了严格措施记录不良事件,干预组和安慰剂对照组都普遍出现短暂的症状加重,这表明这反映了参与试验对患有运动后症状加重疾病的人的影响。某些特定症状,尤其是头痛,确实在使用IgG时更常见,并且可能与有效治疗同时发生,与临床改善相关。这项综述得出的结果得到了与严重和非常严重的ME/CFS患者治疗相关的临床观察结果的支持,对于这些患者,肌肉注射和皮下注射提供了替代选择。我们得出以下结论:(1)有充分理由恢复该领域的研究;(2)在进一步研究之前,临床医生有理由为病情较为严重的部分ME/CFS患者提供一个疗程的IgG治疗。由于大多数试验参与者经历过急性病毒感染或类似病毒感染的发病过程,我们进一步建议,IgG治疗可能适用于一些感染SARS-CoV-2病毒后仍患病的患者的护理。