Longitudinal analysis of SARS-CoV-2 vaccine breakthrough infections reveal limited infectious virus shedding and restricted tissue distribution

Author:

Ke RuianORCID,Martinez Pamela P.,Smith Rebecca L.,Gibson Laura L.,Achenbach Chad J.,McFall Sally,Qi Chao,Jacob Joshua,Dembele Etienne,Bundy Camille,Simons Lacy M.,Ozer Egon A.ORCID,Hultquist Judd F.,Lorenzo-Redondo Ramon,Opdycke Anita K.,Hawkins Claudia,Murphy Robert L.,Mirza Agha,Conte Madison,Gallagher Nicholas,Luo Chun Huai,Jarrett Junko,Conte Abigail,Zhou Ruifeng,Farjo Mireille,Rendon Gloria,Fields Christopher J.,Wang Leyi,Fredrickson Richard,Baughman Melinda E.,Chiu Karen K.,Choi Hannah,Scardina Kevin R.,Owens Alyssa N.,Broach John,Barton Bruce,Lazar Peter,Robinson Matthew L.ORCID,Mostafa Heba H.,Manabe Yukari C.,Pekosz AndrewORCID,McManus David D.,Brooke Christopher B.ORCID

Abstract

ABSTRACTThe global effort to vaccinate people against SARS-CoV-2 in the midst of an ongoing pandemic has raised questions about the nature of vaccine breakthrough infections and the potential for vaccinated individuals to transmit the virus. These questions have become even more urgent as new variants of concern with enhanced transmissibility, such as Delta, continue to emerge. To shed light on how vaccine breakthrough infections compare with infections in immunologically naive individuals, we examined viral dynamics and infectious virus shedding through daily longitudinal sampling in a small cohort of adults infected with SARS-CoV-2 at varying stages of vaccination. The durations of both infectious virus shedding and symptoms were significantly reduced in vaccinated individuals compared with unvaccinated individuals. We also observed that breakthrough infections are associated with strong tissue compartmentalization and are only detectable in saliva in some cases. These data indicate that vaccination shortens the duration of time of high transmission potential, minimizes symptom duration, and may restrict tissue dissemination.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3