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|    Message 811 of 1,639    |
|    Roody Poot Poot to All    |
|    COVID is SARS and liberals are only too     |
|    30 Dec 21 23:09:24    |
      XPost: alt.health.virus.cure.alternatives, rec.sport.football.college       From: easypost@yahoo.com              The SARS-CoV-2 delta (B.1.617.2) variant is highly transmissible and       spreading globally, including in populations with high vaccination       rates. We aimed to investigate transmission and viral load kinetics       in vaccinated and unvaccinated individuals with mild delta variant       infection in the community.              Methods       Between Sept 13, 2020, and Sept 15, 2021, 602 community contacts       (identified via the UK contract-tracing system) of 471 UK COVID-19       index cases were recruited to the Assessment of Transmission and       Contagiousness of COVID-19 in Contacts cohort study and contributed       8145 upper respiratory tract samples from daily sampling for up to       20 days. Household and non-household exposed contacts aged 5 years       or older were eligible for recruitment if they could provide       informed consent and agree to self-swabbing of the upper respiratory       tract. We analysed transmission risk by vaccination status for 231       contacts exposed to 162 epidemiologically linked delta variant-       infected index cases. We compared viral load trajectories from fully       vaccinated individuals with delta infection (n=29) with unvaccinated       individuals with delta (n=16), alpha (B.1.1.7; n=39), and pre-alpha       (n=49) infections. Primary outcomes for the epidemiological analysis       were to assess the secondary attack rate (SAR) in household contacts       stratified by contact vaccination status and the index cases’       vaccination status. Primary outcomes for the viral load kinetics       analysis were to detect differences in the peak viral load, viral       growth rate, and viral decline rate between participants according       to SARS-CoV-2 variant and vaccination status.              Findings       The SAR in household contacts exposed to the delta variant was 25%       (95% CI 18–33) for fully vaccinated individuals compared with 38%       (24–53) in unvaccinated individuals. The median time between second       vaccine dose and study recruitment in fully vaccinated contacts was       longer for infected individuals (median 101 days [IQR 74–120]) than       for uninfected individuals (64 days [32–97], p=0·001). SAR among       household contacts exposed to fully vaccinated index cases was       similar to household contacts exposed to unvaccinated index cases       (25% [95% CI 15–35] for vaccinated vs 23% [15–31] for unvaccinated).       12 (39%) of 31 infections in fully vaccinated household contacts       arose from fully vaccinated epidemiologically linked index cases,       further confirmed by genomic and virological analysis in three index       case–contact pairs. Although peak viral load did not differ by       vaccination status or variant type, it increased modestly with age       (difference of 0·39 [95% credible interval –0·03 to 0·79] in peak       log10 viral load per mL between those aged 10 years and 50 years).       Fully vaccinated individuals with delta variant infection had a       faster (posterior probability >0·84) mean rate of viral load decline       (0·95 log10 copies per mL per day) than did unvaccinated individuals       with pre-alpha (0·69), alpha (0·82), or delta (0·79) variant       infections. Within individuals, faster viral load growth was       correlated with higher peak viral load (correlation 0·42 [95%       credible interval 0·13 to 0·65]) and slower decline (–0·44 [–0·67 to       –0·18]).              Interpretation       Vaccination reduces the risk of delta variant infection and       accelerates viral clearance. Nonetheless, fully vaccinated       individuals with breakthrough infections have peak viral load       similar to unvaccinated cases and can efficiently transmit infection       in household settings, including to fully vaccinated contacts.       Host–virus interactions early in infection may shape the entire       viral trajectory.              Funding       National Institute for Health Research.              https://www.thelancet.com/journals/laninf/article/PIIS1473-3099       (21)00648-4/fulltext              --- SoupGate-Win32 v1.05        * Origin: you cannot sedate... all the things you hate (1:229/2)    |
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