P-2051. Assessing SARS-CoV-2 Correlates Protection from Exposed Household Members: A Prospective Cohort Study (AB-PROTECT Study)

Abstract Background The protection afforded by COVID-19 vaccination wanes over time and varies by SARS-CoV-2 strain. Identifying a marker to serve as an immunologic correlate of protection (CoP) is crucial to ensure future vaccine iterations are sufficiently protective and to inform recommendations for the timing of subsequent vaccine doses.Figure 1.Antibody titres.The probability of COVID-19 by log transformed anti-Spike and anti-RBD IgG titres with raw values represented by dots. Methods A prospective cohort of asymptomatic adults exposed to a household member with COVID-19 was created in Toronto, Ontario from October 1, 2021 until February 21, 2023. At enrolment, anti-spike and anti-receptor binding domain (RBD) IgG titres were measured as were pseudoneutralization titres against wild-type, BA.1 and BA.5 strains for those who provided serum. Participants were followed for 28 days with molecular or antigen testing performed if COVID-19 symptoms arose. A convalescent DBS was collected to assess for asymptomatic infection to compare acute and convalescent anti-nucleoprotein IgG titres. The probability of contracting COVID-19 was modeled using a binomial generalized additive model with a logit link and a thin plate spline on log transformed antibody titres adjusted for whether mitigation measures were employed.Figure 2.Pseudoneutralization Titres.The probability of COVID-19 by log transformed SARS-CoV-2 wild-type pseudoneutralization antibody titres for the entire cohort and households with a circulating Omicron variant. Results In total, 432 individuals from 311 households participated, of which 210 developed COVID-19. The median age was 43 (interquartile range 38-50), 67% (288/432) received 3 vaccine doses, 65% (280/432) were a parent of the index case and 51% (222/432) employed a mitigation measure. There was no difference in the probability of infection by Spike or RBD titres (Figure 1). The difference in probability of COVID for Spike IgG between the 90th (8.83) and 10th percentiles (5.76) is 1.01 (95% CI 0.9 - 1.15, p = 0.84). For RBD IgG the difference between 90th (8.17) and 10th percentiles (5.27) is 1.01 (95% CI 0.89 - 1.14, p = 0.87). Wild-type pseudoneutralization titres also did not confer protection (Figure 2). No differences were identified by circulating household SARS-CoV-2 variant or by pseudoneutralization strain. Conclusion Vaccine derived immune markers of asymptomatic household contacts do not correlate with protection against COVID-19. This could be due to the nonexistence of humoral correlates, rapid rise in antibody titres during the pre-symptomatic phase, or changes in behaviour overrides immune protection. Disclosures Allison McGeer, MD, AstraZeneca: Honoraria|GSK: Honoraria|Merck: Honoraria|Moderna: Honoraria|Novavax: Honoraria|Pfizer: Grant/Research Support|Pfizer: Honoraria|Roche: Honoraria|Seqirus: Grant/Research Support|Seqirus: Honoraria

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Journal
Open Forum Infectious Diseases
Published
2025-01-29
DOI
https://doi.org/10.1093/ofid/ofae631.2207
Primary Topic
COVID-19 Pandemic Impacts
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article

P-2051. Assessing SARS-CoV-2 Correlates Protection from Exposed Household Members: A Prospective Cohort Study (AB-PROTECT Study)

Angel Li, Yaejin Lee, Andrea Llanes, Allison McGeer et al.
Open Forum Infectious Diseases
COVID-19 Pandemic Impacts
article

P-2051. Assessing SARS-CoV-2 Correlates Protection from Exposed Household Members: A Prospective Cohort Study (AB-PROTECT Study)

Angel Li, Yaejin Lee, Andrea Llanes, Allison McGeer, Christopher Kandel, Maureen Taylor, Jeff Powis, Robert W. Kozak, Wenqi Shi, Alexandra Kurtesi, Queenie Hu, Tulunay Tursun, Melanie Delgado-Brand, Geneviève Mailhot, Karen Colwill, Anne‐Claude Gingras, Freda Qi, Maxime Lefebvre, Helen Elliott, Janine McCready, Gloria Crowl
article en

Abstract

Abstract Background The protection afforded by COVID-19 vaccination wanes over time and varies by SARS-CoV-2 strain. Identifying a marker to serve as an immunologic correlate of protection (CoP) is crucial to ensure future vaccine iterations are sufficiently protective and to inform recommendations for the timing of subsequent vaccine doses.Figure 1.Antibody titres.The probability of COVID-19 by log transformed anti-Spike and anti-RBD IgG titres with raw values represented by dots. Methods A prospective cohort of asymptomatic adults exposed to a household member with COVID-19 was created in Toronto, Ontario from October 1, 2021 until February 21, 2023. At enrolment, anti-spike and anti-receptor binding domain (RBD) IgG titres were measured as were pseudoneutralization titres against wild-type, BA.1 and BA.5 strains for those who provided serum. Participants were followed for 28 days with molecular or antigen testing performed if COVID-19 symptoms arose. A convalescent DBS was collected to assess for asymptomatic infection to compare acute and convalescent anti-nucleoprotein IgG titres. The probability of contracting COVID-19 was modeled using a binomial generalized additive model with a logit link and a thin plate spline on log transformed antibody titres adjusted for whether mitigation measures were employed.Figure 2.Pseudoneutralization Titres.The probability of COVID-19 by log transformed SARS-CoV-2 wild-type pseudoneutralization antibody titres for the entire cohort and households with a circulating Omicron variant. Results In total, 432 individuals from 311 households participated, of which 210 developed COVID-19. The median age was 43 (interquartile range 38-50), 67% (288/432) received 3 vaccine doses, 65% (280/432) were a parent of the index case and 51% (222/432) employed a mitigation measure. There was no difference in the probability of infection by Spike or RBD titres (Figure 1). The difference in probability of COVID for Spike IgG between the 90th (8.83) and 10th percentiles (5.76) is 1.01 (95% CI 0.9 - 1.15, p = 0.84). For RBD IgG the difference between 90th (8.17) and 10th percentiles (5.27) is 1.01 (95% CI 0.89 - 1.14, p = 0.87). Wild-type pseudoneutralization titres also did not confer protection (Figure 2). No differences were identified by circulating household SARS-CoV-2 variant or by pseudoneutralization strain. Conclusion Vaccine derived immune markers of asymptomatic household contacts do not correlate with protection against COVID-19. This could be due to the nonexistence of humoral correlates, rapid rise in antibody titres during the pre-symptomatic phase, or changes in behaviour overrides immune protection. Disclosures Allison McGeer, MD, AstraZeneca: Honoraria|GSK: Honoraria|Merck: Honoraria|Moderna: Honoraria|Novavax: Honoraria|Pfizer: Grant/Research Support|Pfizer: Honoraria|Roche: Honoraria|Seqirus: Grant/Research Support|Seqirus: Honoraria

Open Forum Infectious DiseasesVol. 12(Supplement_1)
Mount Sinai Hospital (CA), Sunnybrook Health Science Centre (CA), University of Toronto (CA), Lunenfeld-Tanenbaum Research Institute (CA), Sinai Hospital (US), Toronto East General Hospital (CA), Health Sciences Centre (CA), Sinai Health System (CA)
Openalex Percentile: Top 98%
COVID-19 Pandemic Impacts
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