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These results suggest that individuals who are immunocompromised with type 2 diabetes (T2D) may need multiple doses of a pneumococcal conjugate vaccine (PCV) to sustain their protection.
Adults with type 2 diabetes (T2D) vaccinated with pneumococcal conjugate vaccine 10 (PCV10) demonstrated a significant protective humoral immune response, though the response was considerably less robust with a more rapid decline in those with T2D compared with non-diabetic controls, according to the results of a study published in Vaccine.1
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Individuals with T2D face increased risk of other comorbid conditions, including pneumococcal infections and invasive pneumococcal diseases such as pneumonia and meningitis. There is a particularly heightened risk of pneumococcal infections, as patients with T2D face a 3-fold increased risk of infections, long hospitalizations, and heightened mortality rates compared to non-diabetic counterparts. Fortunately, multiple effective formulations of PCVs are available for adults and pediatrics, though current literature on pneumococcal vaccine responses in patients with T2D is lacking.2,3
While some past authors have observed heightened serotype-specific antibody titers in patients with T2D compared with healthy counterparts following a pneumococcal polysaccharide vaccine (PPV), there has also been high variability in baseline concentrations and antibody functionality in T2D reported by investigators. Overall, there is limited evidence regarding the immunogenicity of PCV10, particularly in T2D diabetes. The current investigators sought to address these gaps through evaluating PCV10 humoral immune responses in a high-T2D-burden, resource-limited setting in Pakistan.1,4,5
According to the investigators, this trial was the first to study PCV10 immunogenicity in such a setting. In total, 180 adults with and without T2D were enrolled in the trial. In an important note, the enrollees did not present with a history of pneumococcal vaccination. At each time point, serotype-specific anti-pneumococcal polysaccharide IgG concentration was measured against pneumococcal serotypes 1, 19F, 9V, and 18C, given the prevalence of these serotypes in the Pakistani population.1
There was a robust humoral response observed against PCV10 and a significantly increased serum IgG against each tested serotype. Furthermore, the antibody concentration remained significantly higher than the baseline level against all 4 serotypes when measured 8 months post-vaccination. Still, when patients were categorized into groups based on the HbA1c values, those without T2D were found to have significantly higher total IgG concentrations than those with T2D following immunization, indicating a less-durable response to the vaccine in the T2D population.1
In their discussion, the investigators pointed to the higher mortality rates among patients with diabetes due to pneumococcal infections to underscore the importance of these results. Above all, the results indicate that PCV10 is effective at increasing serotype-specific IgG concentration up to 8 months post-vaccination in adults both with and without T2D. However, there was a meaningful decrease in protection after 8 months in patients with T2D, “suggesting an altered immune response to vaccination in those with T2D,” according to the investigators.1
There were some limitations reported by the investigators, most prominently the fact that the single-center study was based on a small sample size. Furthermore, there were only 8 months of follow-up; a longer amount of time following vaccination for evaluation could present more thorough outcomes. Still, these results indicate the importance of repeated pneumococcal vaccination in patients with immunocompromised conditions, including T2D.1