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Clinical Trial
. 2022 Aug 24;226(2):287-291.
doi: 10.1093/infdis/jiaa783.

Intestinal Antibody Responses to 2 Novel Live Attenuated Type 2 Oral Poliovirus Vaccines in Healthy Adults in Belgium

Affiliations
Clinical Trial

Intestinal Antibody Responses to 2 Novel Live Attenuated Type 2 Oral Poliovirus Vaccines in Healthy Adults in Belgium

Elizabeth B Brickley et al. J Infect Dis. .

Abstract

In a blinded phase 1 trial (EudraCT 2017-0000908-21; NCT03430349) in Belgium, healthy adults (aged 18-50 years) previously immunized exclusively with inactivated poliovirus vaccine were administered a single dose of 1 of 2 novel type 2 oral poliovirus vaccines (nOPV2-c1: S2/cre5/S15domV/rec1/hifi3 (n = 15); nOPV2-c2: S2/S15domV/CpG40 (n = 15)) and isolated for 28 days in a purpose-built containment facility. Using stool samples collected near days 0, 14, 21, and 28, we evaluated intestinal neutralization and immunoglobulin A responses to the nOPV2s and found that nOPV2-c1 and nOPV2-c2 induced detectable poliovirus type 2-specific intestinal neutralizing responses in 40.0% and 46.7% of participants, respectively.

Keywords: eradication; intestinal antibodies; live attenuated vaccine; mucosal immunity; poliovirus.

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Figures

Figure 1.
Figure 1.
Reverse cumulative distribution functions of poliovirus type 2–specific stool neutralizing activity and immunoglobulin A (IgA) levels before and after receiving nOPV2-c1 (n = 15) (A, B) or nOPV2-c2 (n = 15) (C, D). Because stool samples were not available for all participants on all days, we described the aggregate of the measurements obtained from samples collected on days −2 to 0 (before vaccination) for day 0, days 12–16 for day 14, days 19–23 for day 21, and days 26–30 for day 28. If ≥2 stool samples were collected within each window for a given participant, we calculated the geometric mean of the stool neutralization titer or IgA mean fluorescence intensity (MFI).

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References

    1. Wright PF, Connor RI, Wieland-Alter WF, et al. . Vaccine-induced mucosal immunity to poliovirus: analysis of cohorts from an open-label, randomised controlled trial in Latin American infants. Lancet Infect Dis 2016; 16:1377–84. - PMC - PubMed
    1. Brickley EB, Wieland-Alter W, Connor RI, et al. . Intestinal immunity to poliovirus following sequential trivalent inactivated polio vaccine/bivalent oral polio vaccine and trivalent inactivated polio vaccine-only immunization schedules: analysis of an open-label, randomized, controlled trial in Chilean infants. Clin Infect Dis 2018; 67:42–50. - PMC - PubMed
    1. Brickley EB, Strauch CB, Wieland-Alter WF, et al. . Intestinal immune responses to type 2 oral polio vaccine (OPV) challenge in infants previously immunized with bivalent OPV and either high-dose or standard inactivated polio vaccine. J Infect Dis 2018; 217:371–80. - PMC - PubMed
    1. Brickley EB, Connor RI, Wieland-Alter WF, et al. . Intestinal antibody responses to a live oral poliovirus vaccine challenge among adults previously immunized with inactivated polio vaccine in Sweden. BMJ Glob Health 2019; 4:e001613. - PMC - PubMed
    1. Macklin GR, Grassly NC, Sutter RW, et al. . Vaccine schedules and the effect on humoral and intestinal immunity against poliovirus: a systematic review and network meta-analysis. Lancet Infect Dis 2019; 19:1121–8. - PubMed

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