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Review
. 2021 Mar 2:16:545-552.
doi: 10.2147/COPD.S283832. eCollection 2021.

Polyvalent Immunoglobulin as a Potential Treatment Option for Patients with Recurrent COPD Exacerbations

Affiliations
Review

Polyvalent Immunoglobulin as a Potential Treatment Option for Patients with Recurrent COPD Exacerbations

Dana Unninayar et al. Int J Chron Obstruct Pulmon Dis. .

Abstract

Chronic obstructive pulmonary disease (COPD) is characterized by chronic airway inflammation and episodes of worsening respiratory symptoms and pulmonary function, termed acute exacerbations of COPD (AECOPD). AECOPD episodes are associated with heightened airway inflammation and are often triggered by infection. A subset of COPD patients develops frequent exacerbations despite maximal existing standard medical therapy. It is therefore clear that a targeted and more effective prevention strategy is needed. Immunoglobulins are glycoprotein molecules that are secreted by B lymphocytes and plasma cells and play a critical role in the adaptive immune response against many pathogens. Altered serum immunoglobulin levels have been observed in patients with immunodeficiencies and inflammatory diseases. Serum immunoglobulin has also been identified as potential biomarkers of AECOPD frequency. Since plasma-derived polyvalent immunoglobulin treatment is effective in preventing recurrent infections in immunodeficient patients and in suppressing inflammation in many inflammatory diseases, it may be conceivable that immunoglobulin treatment may be effective in preventing recurrent AECOPD. In this article, we provide a review of the current knowledge on immunoglobulin treatment in patients with COPD and discuss plausible mechanisms as to how immunoglobulin treatment may work to reduce AECOPD frequency.

Keywords: chronic obstructive pulmonary disease; exacerbation; immunoglobulin treatment.

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Conflict of interest statement

DWC and JC received grant funding through our institution (OHRI) from CSL Behring and Grifols for an investigator-sponsored clinical trial of IVIG in recurrent AECOPD. No influence or conflict exists, but might be perceived. JC reports grants from CSL Behring, grants from Grifols, grants from Takeda, grants and personal fees from OctaPharma, personal fees from GSK, personal fees from Sanofi, personal fees from Alexion Pharma, personal fees from EMD Serono outside the submitted work. DU and SJA do not have competing interests to declare.

Figures

Figure 1
Figure 1
Author’s proposed hypothesis. Humoral immunodeficiency is more prevalent in COPD patients with “high-risk of exacerbations phenotype” than those with a “low-risk of exacerbations phenotype”.

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