Abstract

BackgroundPatients living with HIV (PLHIV) are prone to invasive pneumococcal disease. The 13-valent conjugated pneumococcal vaccine (PCV13) is currently recommended for all PLHIV, followed in most guidelines by a 23-valent polysaccharide pneumococcal vaccine. Data are scarce concerning the immunological efficacy of PCV13 among PLHIV.ObjectiveTo assess the immunological response at one month, and the immunological protection at 1-, 6-, and 12 months in PLHIV with a CD4 cell count above 200 cells/µl after a single dose of PCV13, as measured by both ELISA and opsonophagocytic assay (OPA).MethodsPLHIV with CD4 cell count >200 cells/µl were included. Specific IgG serum concentrations for eight serotypes by ELISA and seven serotypes by OPA were measured at baseline, 1-, 6-, and 12 months after the PCV13 vaccination. Global response was defined as a two-fold increase from baseline of specific IgG antibody levels (μg/ml) assayed by ELISA or as a four-fold increase in OPA titer from baseline, for at least five serotypes targeted by PCV13. Global protection was defined as an IgG-concentration ≥1 µg/ml by ELISA or as an opsonization titer ≥LLOQ by OPA for at least five tested serotypes targeted by PCV13. Factors associated with global response and global protection were assessed using logistic regression.ResultsOf the 38 PLHIV included, 57.9% and 63.2% were global responders, 92.1% and 78.9% were globally protected at one month, and 64.7% and 55.9% were still protected at 12 months, by ELISA and OPA respectively. A CD4/CD8 ratio of >0.8 was significantly associated with a better global response by OPA (OR=6.11, p=0.02), and a CD4 nadir <200 was significantly associated with a poorer global response by ELISA (OR=0.22, p=0.04). A CD4 cell count nadir <200 and age over 50 years were associated with poorer global protection by OPA at M1 (OR=0.18, p=0.04) and M12 (OR= 0.15, p=0.02), respectively. Plasma HIV RNA viral load <40 copies/ml was significantly associated with a better global protection at M1 by ELISA and OPA (OR=21.33, p=0.025 and OR=8.40, p=0.04)ConclusionVaccination with PCV13 in these patients induced immunological response and protection at one month. At one year, more than half of patients were still immunologically protected.

Highlights

  • Streptococcus pneumoniae, formerly known as pneumococcus, causes severe infections such as bacterial pneumonia and invasive pneumococcal diseases (IPD) including meningitis, arthritis, and bacteremia

  • -Global responder to the vaccine by enzyme-linked immunosorbent assay (ELISA) or opsonophagocytic assay (OPA) was defined as a patient who developed a response for at least five of the tested serotypes targeted by PCV13

  • -Global protection by ELISA or OPA was defined by a protection for at least five of the tested serotypes targeted by PCV13

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Summary

Introduction

Streptococcus pneumoniae, formerly known as pneumococcus, causes severe infections such as bacterial pneumonia and invasive pneumococcal diseases (IPD) including meningitis, arthritis, and bacteremia. They are responsible for a high morbidity and mortality burden. S.pneumoniae possess a polysaccharide (PS) pneumococcal capsule which partly explains its virulence. People living with HIV (PLHIV) are at higher risk of invasive pneumococcal diseases (IPD) than the general population. Factors likely to explain these differences are loss of memory cells, persistent inflammation, and nasopharyngeal pneumococcal carriage [5, 6]. Patients living with HIV (PLHIV) are prone to invasive pneumococcal disease. Data are scarce concerning the immunological efficacy of PCV13 among PLHIV

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