Persistent IgG anticardiolipin autoantibodies are associated with post-COVID syndrome
•To date, no biological markers have been proposed to predict post-coronavirus disease 2019 (COVID-19) syndrome (PCS).•Immunoglobulin G (IgG) anticardiolipin autoantibodies (aCL) are associated with the severity of COVID-19.•This article reports a case of persistent IgG aCL positivity in a patient w...
Saved in:
Published in | International journal of infectious diseases Vol. 113; pp. 23 - 25 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Canada
Elsevier Ltd
01.12.2021
Elsevier The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | •To date, no biological markers have been proposed to predict post-coronavirus disease 2019 (COVID-19) syndrome (PCS).•Immunoglobulin G (IgG) anticardiolipin autoantibodies (aCL) are associated with the severity of COVID-19.•This article reports a case of persistent IgG aCL positivity in a patient with PCS.•Persistence of aCL positivity could be a biological predictor of PCS.
Persistence of various symptoms in patients who have recovered from coronavirus disease 2019 (COVID-19) was recently defined as ‘long COVID’ or ‘post-COVID syndrome’ (PCS). This article reports a case of a 58-year-old woman who, although recovering from COVID-19, had novel and persistent symptoms including neurological complications that could not be explained by any cause other than PCS. In addition to a low inflammatory response, persistence of immunoglobulin G anticardiolipin autoantibody positivity and eosinopenia were found 1 year after acute COVID-19 infection, both of which have been defined previously as independent factors associated with the severity of COVID-19. The pathophysiological mechanism of PCS is unknown, but the possibility of persistence of the virus, especially in the nervous system, could be suggested with a post-infectious inflammatory or autoimmune reaction. |
---|---|
Bibliography: | PMCID: PMC8487460 |
ISSN: | 1201-9712 1878-3511 |
DOI: | 10.1016/j.ijid.2021.09.079 |