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Published on: August 30, 2018
Antiphospholipid Antibodies in Critically Ill Patients With COVID-19
Meng Xiao1, Yan Zhang1, Shulan Zhang1
1Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Insights
Antiphospholipid antibodies (aPLs) were found in 47% of critically ill COVID-19 patients, with IgA anti-β2 GPI being the most common. These antibodies may indicate a higher risk of cerebral infarction in severe COVID-19 cases.
Area of Science:
- Immunology
- Virology
- Critical Care Medicine
Background:
- Coagulopathy is a known complication in critically ill COVID-19 patients.
- The role of antiphospholipid antibodies (aPLs) in COVID-19-associated coagulopathy is not fully understood.
Purpose of the Study:
- To determine the prevalence and characteristics of aPLs in patients with COVID-19.
- To investigate the association between aPLs and severe outcomes in COVID-19.
Main Methods:
- Sera from 66 critically ill and 13 non-critically ill COVID-19 patients were tested for various aPLs using chemiluminescence immunoassay and ELISA.
- Antibody detection included anticardiolipin antibodies (aCLs), anti-β2-glycoprotein I (anti-β2 GPI), and anti-phosphatidylserine/prothrombin (anti-PS/PT).
Main Results:
- aPLs were detected in 47% of critically ill COVID-19 patients, but none in non-critically ill patients.
- IgA anti-β2 GPI was the most prevalent aPL (28.8%), followed by IgA aCLs (25.8%) and IgG anti-β2 GPI (18.2%).
- Patients with multiple aPLs had a significantly higher incidence of cerebral infarction (P=0.023).
Conclusions:
- Antiphospholipid antibodies are common in critically ill COVID-19 patients and may be transient.
- The presence of multiple aPLs or high titers could identify patients at risk for cerebral infarction.
- COVID-19 may trigger an antiphospholipid syndrome-like condition in susceptible individuals.
Objective:
Coagulopathy is one of the characteristics observed in critically ill patients with coronavirus disease 2019 (COVID-19). Antiphospholipid antibodies (aPLs) contribute to coagulopathy, though their role in COVID-19 remains unclear. This study was undertaken to determine the prevalence and characteristics of aPLs in patients with COVID-19.
Methods:
Sera collected from 66 COVID-19 patients who were critically ill and 13 COVID-19 patients who were not critically ill were tested by chemiluminescence immunoassay for anticardiolipin antibodies (aCLs), anti-β2 -glycoprotein I (anti-β2 GPI) (IgG, IgM, and IgA), and IgG anti-β2 GPI-domain 1 (anti-β2 GPI-D1) and IgM and IgG anti-phosphatidylserine/prothrombin (anti-PS/PT) antibodies were detected in the serum by enzyme-linked immunosorbent assay.
Results:
Of the 66 COVID-19 patients in critical condition, aPLs were detected in 31 (47% ). Antiphospholipid antibodies were not present among COVID-19 patients who were not in critical condition. The IgA anti-β2 GPI antibody was the most commonly observed aPL in patients with COVID-19 and was present in 28.8% (19 of 66) of the critically ill patients, followed by IgA aCLs (17 of 66, or 25.8%) and IgG anti-β2 GPI (12 of 66, or 18.2%). For multiple aPLs, IgA anti-β2 GPI + IgA aCLs was the most common antibody profile observed (15 of 66, or 22.7%), followed by IgA anti-β2 GPI + IgA aCL + IgG anti-β2 GPI (10 of 66, or 15.2%). Antiphospholipid antibodies emerge ~35-39 days after disease onset. A dynamic analysis of aPLs revealed 4 patterns based on the persistence or transient appearance of the aPLs. Patients with multiple aPLs had a significantly higher incidence of cerebral infarction compared to patients who were negative for aPLs (P = 0.023).
Conclusion:
Antiphospholipid antibodies were common in critically ill patients with COVID-19. Repeated testing demonstrating medium to high titers of aPLs and the number of aPL types a patient is positive for may help in identifying patients who are at risk of developing cerebral infarction. Antiphospholipid antibodies may be transient and disappear within a few weeks, but in genetically predisposed patients, COVID-19 may trigger the development of an autoimmune condition similar to the antiphospholipid syndrome (APS), referred to as "COVID-19-induced APS-like syndrome." Long-term follow-up of COVID-19 patients who are positive for aPLs would be of great importance in understanding the pathogenesis of this novel coronavirus.
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