Seroconversion and antibody persistence after yellow fever vaccination in people living with HIV: impact of baseline HIV viral load and yellow fever seropositivity

Author:

Martin Charlotte12ORCID,Florence Eric3,Domingo Cristina45,Delforge Marc12,De Wit Stéphane12,Dauby Nicolas126787

Affiliation:

1. Infectious Diseases Department , Saint-Pierre University Hospital, , 1000 Brussels , Belgium

2. Université Libre de Bruxelles (ULB) , Saint-Pierre University Hospital, , 1000 Brussels , Belgium

3. Institute of Tropical Medicine , 2000 Antwerp , Belgium

4. Robert Koch Institute, Centre for Biological Threats and Special Pathogens - Highly Pathogenic Viruses- ZBS-1 , 13353 Berlin , Germany

5. Robert Koch Institute, Centre for International Health Protection (ZIG) -ZIG-4 Public Health Laboratory Support , 13353 Berlin , Germany

6. Institute for Medical Immunology , , 1070 Brussels , Belgium

7. Université Libre de Bruxelles (ULB) , , 1070 Brussels , Belgium

8. School of Public Health , , 1070 Brussels , Belgium

Abstract

Abstract Background Data on seroconversion rates following yellow fever (YF) vaccine and effect of revaccination in people living with HIV (PLWH) are scarce. We aimed at determining key factors for seroconversion after YF vaccine in PLWH and the role of preexisting neutralizing antibodies (NAbs) at vaccination. Methods A retrospective cross-sectional study at several timepoints in two Belgian AIDS Reference Center. For each individual, plasma samples from three timepoints were selected: Timepoint 0 (TP0) in the year before administration of the YF vaccine, Timepoint 1 (TP1) in the year following the YF vaccine, Timepoint 2 (TP2) >1 year after the YF vaccine. Plasma samples were analysed for YF NAbs by plaque reduction neutralization test. The primary endpoint was the number of patients with protective levels of NAbs ≥ 1/10. A boosted immune response was defined as a 4-fold increase in serologic titres following revaccination. Results Of the 160 PLWH included, protective levels of NAbs were present in 36%, 87% and 72% of subjects at baseline, at a median of 12 months and a median of 96 months after YF vaccination, respectively. Among vaccine recipients negative for YF NAbs at baseline (n = 102), 83% seroconverted. PLWH with undetectable HIV viral load (VL) at baseline were more likely to seroconvert (P < 0·01). A booster response was observed in only 17% of subjects with baseline seropositivity (n = 10 out of 58). In multivariate analysis, undetectable HIV VL at vaccination and baseline YF seropositivity were associated with persistent levels of protective NAbs at a median of 8 years after YF vaccination. Conclusion Undetectable HIV VL at baseline is associated with high rates of seroconversion. YF seropositivity before revaccination is associated with low rates of booster effect but a higher chance of long term persistent NAbs response, suggesting a benefit of revaccination in PLWH.

Funder

International Society of Travel Medicine

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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