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Limited Innovations After More Than 65 Years of Immunoglobulin Replacement Therapy: Potential of IgA- and IgM-Enriched Formulations to Prevent Bacterial Respiratory Tract Infections

机译:65多年免疫球蛋白替代治疗后的有限创新:IGA-和IgM-富集的配方的潜力,以防止细菌呼吸道感染

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摘要

Patients with primary immunoglobulin deficiency have lower immunoglobulin levels or decreased immunoglobulin function, which makes these patients more susceptible to bacterial infection. Most prevalent are the selective IgA deficiencies (~1:3,000), followed by common variable immune deficiency (~1:25,000). Agammaglobulinemia is less common (~1:400,000) and is characterized by very low or no immunoglobulin production resulting in a more severe disease phenotype. Therapy for patients with agammaglobulinemia mainly relies on prophylactic antibiotics and the use of IgG replacement therapy, which successfully reduces the frequency of invasive bacterial infections. Currently used immunoglobulin preparations contain only IgG. As a result, concurrent IgA and IgM deficiency persist in a large proportion of agammaglobulinemia patients. Especially patients with IgM deficiency remain at risk for recurrent infections at mucosal surfaces, which includes the respiratory tract. IgA and IgM have multiple functions in the protection against bacterial infections at the mucosal surface. Because of their multimeric structure, both IgA and IgM are able to agglutinate bacteria efficiently. Agglutination allows for entrapment of bacteria in mucus that increases clearance from the respiratory tract. IgA is also important for blocking bacterial adhesion by interfering with bacterial adhesion receptors. IgM in its place is very well capable of activating complement, therefore, it is thought to be important in complement-mediated protection at the mucosal surface. The purpose of this Mini Review is to highlight the latest advances regarding IgA- and IgM-enriched immunoglobulin replacement therapy. We describe the different IgA- and IgM-enriched IgG formulations, their possible modes of action and potential to protect against respiratory tract infections in patients with primary immunoglobulin deficiencies.
机译:患有初级免疫球蛋白缺乏的患者具有较低的免疫球蛋白水平或降低免疫球蛋白功能,使这些患者更容易受细菌感染。最普遍的是选择性IgA缺陷(〜1:3,000),其次是常见的可变免疫缺陷(〜1:25,000)。 Agammaglobulinemia不太常见(〜1:400,000),其特征在于非常低或没有免疫球蛋白产生,导致更严重的疾病表型。 Agammaglobobulinemia患者的治疗主要依赖于预防性抗生素和IgG替代治疗的使用,从而成功降低了侵袭性细菌感染的频率。目前使用的免疫球蛋白制剂仅含有IgG。结果,同时IgA和IgM缺乏持续存在于大部分Agammaglobulinemia患者。特别是IgM缺乏患者仍然有粘膜表面经常感染的风险,包括呼吸道。 IgA和IgM在保护粘膜表面的细菌感染方面具有多种功能。由于它们的多聚体结构,IgA和IgM都能够有效地凝集细菌。凝集允许在粘液中捕获细菌,从而增加呼吸道的间隙。 IgA对于通过干扰细菌粘附受体阻断细菌粘附也很重要。 IgM在其位置非常好,能够激活补体,因此,认为在粘膜表面的补充介导的保护中是重要的。该迷你审查的目的是突出富含IgA和IgM的免疫球蛋白替代疗法的最新进展。我们描述了不同的IgA和IgM富集的IgG制剂,其可能的作用方式和潜力,以防止患有原发性免疫球蛋白缺陷患者的呼吸道感染。

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