@article{518157419fc44b08ac6c8cbf540105eb,
title = "SARS-CoV-2 Spike-Binding Antibody Longevity and Protection from Reinfection with Antigenically Similar SARS-CoV-2 Variants",
abstract = "The PARIS (Protection Associated with Rapid Immunity to SARS-CoV-2) cohort follows health care workers with and without documented coronavirus disease 2019 (COVID-19) since April 2020. We report our findings regarding severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike-binding antibody stability and protection from infection in the pre-variant era. We analyzed data from 400 health care workers (150 seropositive and 250 seronegative at enrollment) for a median of 84 days. The SARS-CoV-2 spike-binding antibody titers were highly variable with antibody levels decreasing over the first 3 months, followed by a relative stabilization. We found that both more advanced age (> 40 years) and female sex were associated with higher antibody levels (1.6-fold and 1.4-fold increases, respectively). Only six percent of the initially seropositive participants “seroreverted.” We documented a total of 11 new SARS-CoV-2 infections (10 naive participants and 1 previously infected participant without detectable antibodies; P < 0.01), indicating that spike antibodies limit the risk of reinfection. These observations, however, only apply to SARS-CoV-2 variants antigenically similar to the ancestral SARS-CoV-2 ones. In conclusion, SARS-CoV-2 antibody titers mounted upon infection are stable over several months and provide protection from infection with antigenically similar viruses. IMPORTANCE SARS-CoV-2 is the cause of one of the largest noninfluenza pandemics of this century. This exceptional public health crisis highlights the urgent need for better understanding of the correlates of protection from infection and severe COVID-19. We established the PARIS cohort to determine durability and effectiveness of SARS-CoV-2 immune responses. Here, we report on the kinetics of SARS-CoV-2 spike-binding antibody after SARS-CoV-2 infection as well as reinfection rates using data collected between April 2020 and August 2021. We found that antibody levels stabilized at individual steady state levels after an initial decrease with seroreversion being found in only 6% of the convalescent participants. SARS-CoV-2 infections only occurred in participants without detectable spike-binding antibodies, indicating significant protection from reinfection with antigenically similar viruses. Our data indicate the importance of spike-binding antibody titers in protection prior to vaccination and the wide circulation of antigenically diverse variants of concern.",
keywords = "COVID-19, SARS-CoV-2, antibody durability, modeling, protection, spike-binding antibodies",
author = "{PARIS Study Team} and John Kubale and Charles Gleason and Carre{\~n}o, {Juan Manuel} and Komal Srivastava and Gagandeep Singh and Aubree Gordon and Florian Krammer and Viviana Simon and Hala Alshammary and Amoako, {Angela A.} and Dalles Andre and Awawda, {Mahmoud H.} and Beach, {Katherine F.} and Bielak, {Dominika A.} and Berm{\'u}dez-Gonz{\'a}lez, {Maria C.} and Cai, {Gianna Y.} and Chernet, {Rachel L.} and Christian Cognigni and Ferreri, {Emily D.} and Floda, {Daniel L.} and Joshua Hamburger and Hisaaki Kawabata and Giulio Kleiner and Neko Lyttle and Mendez, {Wanni A.} and Mulder, {Lubbertus C.F.} and Ismail Nabeel and Annika Oostenink and Ariel Raskin and Aria Rooker and Kayla Russo and Salimbangon, {Ashley Beathrese T.} and Miti Saksena and Sominsky, {Levy A.} and Daniel Stadlbauer and Johnstone Tcheou and Ania Wajnberg",
note = "Funding Information: We thank the study participants for their generosity and willingness to participate in longitudinal COVID-19 research studies. None of this work would be possible without their contributions. We are very appreciative of the support of Mount Sinai's leadership throughout the COVID-19 pandemic. We want to especially thank Peter Palese, Carlos Cordon-Cardo, Dennis Charney, David Reich, and Kenneth Davis. We also thank Daniel Caughey for expert administrative assistance and Andrew Brouwer for his thoughtful comments and suggestions. This work is part of the PARIS/SPARTA studies funded by NIAID Collaborative Influenza Vaccine Innovation Centers (CIVIC) contract 75N93019C00051. In addition, this work was also partially funded by the NIAID Centers of Excellence for Influenza Research and Response (CEIRR) contract 75N93021C00014 as well as by anonymous donors. This work is part of the NIAID SARS-CoV-2 Assessment of Viral Evolution (SAVE) program. The Icahn School of Medicine at Mount Sinai has filed patent applications relating to SARS-CoV-2 serological assays (U.S. provisional application numbers 62/994, 252, 63/018, 457, 63/020, 503, and 63/024, 436) and NDV-based SARS-CoV-2 vaccines (U.S. provisional application number 63/251, 020), which list Florian Krammer as co-inventor. Viviana Simon is also listed on the serological assay patent application as coinventor. Patent applications were submitted by the Icahn School of Medicine at Mount Sinai. Mount Sinai has spun out a company, Kantaro, to market serological tests for SARS-CoV-2. Florian Krammer has consulted for Merck and Pfizer (before 2020) and is currently consulting for Pfizer, Third Rock Ventures, Seqirus, and Avimex. The Krammer laboratory is also collaborating with Pfizer on animal models of SARS-CoV-2. Aubree Gordon serves on a scientific advisory board for Janssen and has consulted for Gilead Sciences. Funding Information: This work is part of the PARIS/SPARTA studies funded by NIAID Collaborative Influenza Vaccine Innovation Centers (CIVIC) contract 75N93019C00051. In addition, this work was also partially funded by the NIAID Centers of Excellence for Influenza Research and Response (CEIRR) contract 75N93021C00014 as well as by anonymous donors. This work is part of the NIAID SARS-CoV-2 Assessment of Viral Evolution (SAVE) program. Publisher Copyright: Copyright {\textcopyright} 2022 Kubale et al.",
year = "2022",
month = sep,
doi = "10.1128/mbio.01784-22",
language = "English",
volume = "13",
journal = "mBio",
issn = "2161-2129",
publisher = "American Society for Microbiology",
number = "5",
}