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Evidence of recent Epstein-Barr virus reactivation in individuals experiencing Long COVID
Michael J Peluso; Tyler-Marie Deveau; Sadie E Munter; Dylan Ryder; Amanda Buck; Gabrielle Beck-Engeser; Fay Chan; Scott Lu; Sarah A Goldberg; Rebecca Hoh; Viva Tai; Leonel Torres; Nikita S Iyer; Monika Deswal; Lynn H Ngo; Melissa Buitrago; Antonio Rodriguez; Jessica Y Chen; Brandon C Yee; Ahmed Chenna; John W Winslow; Christos J Petropoulos; Amelia N Deitchman; Joanna Hellmuth; Matthew A Spinelli; Matthew S Durstenfeld; Priscilla Y Hsue; J Daniel Kelly; Jeffrey N Martin; Steven G Deeks; Peter W Hunt; Timothy J Henrich.
Afiliação
  • Michael J Peluso; University of California, San Francisco
  • Tyler-Marie Deveau; University of California, San Francisco
  • Sadie E Munter; University of California, San Francisco
  • Dylan Ryder; University of California, San Francisco
  • Amanda Buck; University of California, San Francisco
  • Gabrielle Beck-Engeser; University of California, San Francisco
  • Fay Chan; University of California, San Francisco
  • Scott Lu; University of California, San Francisco
  • Sarah A Goldberg; University of California, San Francisco
  • Rebecca Hoh; University of California, San Francisco
  • Viva Tai; University of California, San Francisco
  • Leonel Torres; University of California, San Francisco
  • Nikita S Iyer; University of California, San Francisco
  • Monika Deswal; University of California, San Francisco
  • Lynn H Ngo; University of California, San Francisco
  • Melissa Buitrago; University of California, San Francisco
  • Antonio Rodriguez; University of California, San Francisco
  • Jessica Y Chen; University of California, San Francisco
  • Brandon C Yee; Monogram Biosciences
  • Ahmed Chenna; Monogram Biosciences
  • John W Winslow; Monogram Biosciences
  • Christos J Petropoulos; Monogram Biosciences
  • Amelia N Deitchman; University of California, San Francisco
  • Joanna Hellmuth; University of California, San Francisco
  • Matthew A Spinelli; University of California, San Francisco
  • Matthew S Durstenfeld; University of California, San Francisco
  • Priscilla Y Hsue; University of California, San Francisco
  • J Daniel Kelly; University of California, San Francisco
  • Jeffrey N Martin; University of California, San Francisco
  • Steven G Deeks; University of California, San Francisco
  • Peter W Hunt; University of California, San Francisco
  • Timothy J Henrich; University of California, San Francisco
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22276660
ABSTRACT
The presence and reactivation of chronic viral infections such as Epstein-Barr virus (EBV), cytomegalovirus (CMV) and human immunodeficiency virus (HIV) have been proposed as potential contributors to Long COVID (LC), but studies in well-characterized post-acute cohorts of individuals with COVID-19 over a longer time course consistent with current case definitions of LC are limited. In a cohort of 280 adults with prior SARS-CoV-2 infection, we observed that LC symptoms such as fatigue and neurocognitive dysfunction at a median of 4 months following initial diagnosis were independently associated with serological evidence of recent EBV reactivation (early antigen-D [EA-D] IgG positivity) or high nuclear antigen IgG levels, but not with ongoing EBV viremia. Evidence of EBV reactivation (EA-D IgG) was most strongly associated with fatigue (OR 2.12). Underlying HIV infection was also independently associated with neurocognitive LC (OR 2.5). Interestingly, participants who had serologic evidence of prior CMV infection were less likely to develop neurocognitive LC (OR 0.52) and tended to have less severe (>5 symptoms reported) LC (OR 0.44). Overall, these findings suggest differential effects of chronic viral co-infections on the likelihood of developing LC and predicted distinct syndromic patterns. Further assessment during the acute phase of COVID-19 is warranted. SUMMARYThe authors found that Long COVID symptoms in a post-acute cohort were associated with serological evidence of recent EBV reactivation and pre-existing HIV infection when adjusted for participant factors, sample timing, comorbid conditions and prior hospitalization, whereas underlying CMV infection was associated with a decreased risk of Long COVID.
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Estudo diagnóstico / Estudo observacional / Estudo prognóstico Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Estudo diagnóstico / Estudo observacional / Estudo prognóstico Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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