DOAJ Open Access 2018

Serotypes With Low Invasive Potential Are Associated With an Impaired Antibody Response in Invasive Pneumococcal Disease

Nils Littorin Fabian Uddén Jonas Ahl Jonas Ahl Fredrik Resman +4 lainnya

Abstrak

Pneumococcal polysaccharide vaccines may elicit a hyporesponse under certain conditions. There is limited knowledge, however, on the type of specific antibody response in individuals with invasive pneumococcal disease (IPD). The aim of this study was to investigate the functional antibody response in patients with IPD caused by different serotypes. Pre-immune and convalescent sera from 40 patients (age 14–91 years) with IPD caused by serotypes with low (serotype 3, 19F, and 23F) and high (1, 4, 7F, and 14) invasive potential were investigated. For each patient, the homologous serotype-specific antibody concentration was determined. The functionality of induced antibodies post-IPD was evaluated in an opsonophagocytic assay (OPA). Undetectable or decreased pneumococcal killing in OPA following IPD, i.e., a nonfunctional antibody response, was observed in 24 of 40 patients (60%). Patients with nonfunctional antibody responses had lower serotype specific IgG antibody ratios post-IPD than patients with increased OPA titres. A nonfunctional antibody response was associated with low invasive serotypes (3, 19F, and 23F, p = 0.015). In conclusion, a nonfunctional antibody response may follow IPD, and was in our cohort associated to serotypes with low invasive potential. These findings need to be confirmed in a larger material.

Topik & Kata Kunci

Penulis (9)

N

Nils Littorin

F

Fabian Uddén

J

Jonas Ahl

J

Jonas Ahl

F

Fredrik Resman

F

Fredrik Resman

H

Hans-Christian Slotved

S

Simon Athlin

K

Kristian Riesbeck

Format Sitasi

Littorin, N., Uddén, F., Ahl, J., Ahl, J., Resman, F., Resman, F. et al. (2018). Serotypes With Low Invasive Potential Are Associated With an Impaired Antibody Response in Invasive Pneumococcal Disease. https://doi.org/10.3389/fmicb.2018.02746

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Informasi Jurnal
Tahun Terbit
2018
Sumber Database
DOAJ
DOI
10.3389/fmicb.2018.02746
Akses
Open Access ✓