4.4 Article

Herpesvirus infections and post-COVID-19 manifestations: a pilot observational study

Journal

RHEUMATOLOGY INTERNATIONAL
Volume 42, Issue 9, Pages 1523-1530

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00296-022-05146-9

Keywords

COVID-19; Herpes virus; Epstein-Barr virus; Rheumatology; An autoimmune disease

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The global spread of SARS-CoV-2 has led to unprecedented mutational variation of the virus, contributing to a variety of post-COVID sequelae in immunocompromised subjects and high mortality. Numerous studies have reported the reactivation of herpes virus infections in COVID-19, which worsen the disease and complicate with lasting post-COVID manifestations. This study aimed to describe the clinical and laboratory features of post-COVID manifestations accompanied by the reactivation of herpes virus infections.
The global spread of SARS-CoV-2 points to unrivaled mutational variation of the virus, contributing to a variety of post-COVID sequelae in immunocompromised subjects and high mortality. Numerous studies have reported the reactivation of sluggish herpes virus infections in COVID-19, which exaggerate the course of the disease and complicate with lasting post-COVID manifestations CMV, EBV, HHV6). This study aimed to describe clinical and laboratory features of post-COVID manifestations accompanied by the reactivation of herpes virus infections (CMV, EBV, HHV6). 88 patients were recruited for this study, including subjects with reactivation of herpes viruses, 68 (72.3%) (main group) and 20 (27.7%) subjects without detectable DNA of herpesviruses (control group): 46 (52.3%) female and 42 (47.7%) male; median age was 41.4 +/- 6.7 years. Patients with post-COVID manifestations presented with reactivation of EBV in 42.6%, HHV6 in 25.0%, and EBV plus HHV6 in 32.4%. Compared with controls, patients with herpes virus infections presented with more frequent slight fever temperature, headache, psycho-neurological disorders, pulmonary abnormalities and myalgia (p < 0.01), activation of liver enzymes, elevated CRP and D-dimer, and suppressed cellular immune response (p <= 0.05). Preliminary results indicate a likely involvement of reactivated herpes virus infections, primarily EBV infections in severe COVID-19 and the formation of the post-COVID syndrome. Patients with the post-COVID syndrome and reactivation of EBV and HHV6 infections are at high risk of developing various pathologies, including rheumatologic diseases.

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