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SARS-CoV-2 infection in singleton pregnant women increases antiphospholipid antibody prevalence and placental dysfunction riskCOVID in Pregnancy May Trigger Clot-Causing Antibodies

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Key Takeaway
Consider aPL screening 2–4 weeks post-infection in third-trimester pregnant women with SARS-CoV-2 and monitor for placental dysfunction.

This prospective, observational cohort study evaluated singleton pregnant women without pre-existing pregnancy complications who tested positive for SARS-CoV-2 infection. Conducted at the Department of Obstetrics, Peking University People's Hospital, the study monitored patients from the time of infection through standard prenatal care protocols. Serum samples were collected 2–4 weeks post-infection to assess antibody status.

The primary outcome measured the prevalence of antiphospholipid antibodies (aPLs) and their impact on maternal-fetal outcomes. Secondary outcomes included positivity for lupus anticoagulant (LAC), anti-β2-glycoprotein I (aβ2GPI), anticardiolipin antibodies, and placental dysfunction complications. The overall prevalence of aPLs was 18.75% among the cohort.

Prevalence varied significantly by gestational stage, rising from 5.88% in the first trimester to 16.00% in the second and 26.31% in the third trimester. All positive cases exhibited single-antibody positivity, specifically for either aβ2GPI or LAC; no instances of multiple antibody co-positivity were observed. Positivity for aPLs, particularly LAC, was identified as an independent risk factor for placental dysfunction-related complications.

No adverse events, serious adverse events, discontinuations, or specific tolerability issues were reported in the provided data. The study notes that aPL positivity is an independent risk factor for complications related to placental dysfunction. While the study design is observational, the association between infection timing, antibody development, and placental dysfunction risk is clear. Clinicians should consider enhanced monitoring for placental dysfunction, vigilant surveillance of infection status and coagulation function, and appropriate obstetric management for infected women, especially those in the third trimester.

A quiet problem after a common infection

You're pregnant. You catch COVID. The cough clears. Life moves on.

But a few weeks later, your placenta — the organ feeding your baby — could be quietly struggling. And you might feel nothing at all.

That's the concern raised by a new Chinese study on pregnant women after SARS-CoV-2 infection.

COVID is still circulating. Most pregnant women who catch it recover without major problems.

But pregnancy changes how the immune system works. And the placenta depends on smooth blood flow through very small vessels. Anything that tips the body toward more clotting can cause trouble.

Antiphospholipid antibodies (antiphospholipid antibodies = immune proteins that can cause clots) are one such trigger. They are already known to cause miscarriage, preeclampsia, and placental problems in some patients.

The old view vs a new signal

Before COVID, antiphospholipid antibodies were mainly studied in people with autoimmune disease like lupus.

But here's the twist. Research during the pandemic showed that viral infections can sometimes kick the immune system into producing these same antibodies, at least temporarily.

This new study asked: how often does that happen in pregnant women, and does it affect the pregnancy?

How it works, in plain terms

Think of the placenta as a sponge full of tiny rivers.

Those rivers need to stay open for your baby to get oxygen and nutrients. Antiphospholipid antibodies are like small sticky clumps that can block the rivers. Fewer open rivers means less delivery.

Lupus anticoagulant (LAC) is one of the most important of these sticky clumps. Despite its name, it actually makes clotting more likely inside the body.

Researchers at Peking University People's Hospital ran a prospective observational cohort study.

They enrolled pregnant women who had a single (not twin) pregnancy, no pre-existing pregnancy complications, and who tested positive for SARS-CoV-2.

Between December 2022 and January 2023, they drew blood 2 to 4 weeks after each woman's COVID infection. They tested for three antibodies: LAC, anti-β2-glycoprotein I, and anticardiolipin. Then they followed outcomes through standard prenatal care.

Overall, about 1 in 5 infected pregnant women — roughly 19% — tested positive for at least one antiphospholipid antibody.

Every positive case showed just a single antibody. No one had multiple positives at the same time. That is actually reassuring: "triple-positive" patients are usually the highest risk.

The rate rose sharply with pregnancy stage. In the first trimester, fewer than 1 in 17 women tested positive. In the second, about 1 in 6. In the third, more than 1 in 4.

That third-trimester signal is the one to pay attention to.

Women who were positive, especially for LAC, had higher rates of placental-related complications. The authors identified LAC positivity as an independent risk factor for those outcomes.

Here's where it gets interesting

Most of these antibody findings may be temporary. Viral infections can cause short-lived "passenger" antibodies that fade.

But during pregnancy, even a temporary push toward clotting can matter. Timing is everything.

Obstetricians have watched carefully since the pandemic began for signs that COVID raises placental risk. This study adds specific, measurable data to those concerns.

The main takeaway fits broader experience: pregnancy plus a new viral infection deserves attentive follow-up, not panic. And later-pregnancy infections may need closer eyes than earlier ones.

If you are pregnant and have had COVID, share the timing with your obstetric team.

Based on this study, it may be reasonable to discuss antiphospholipid antibody testing 2 to 4 weeks after infection, especially if your infection was in the third trimester. Ask your provider.

Watch for signs of placental trouble: decreased fetal movement, sudden swelling, severe headaches, visual changes, or high blood pressure. Report them quickly. Standard prenatal monitoring becomes even more valuable in this setting.

This study does not suggest every pregnant woman with COVID develops complications. It identifies a subgroup that may benefit from extra attention.

This was a single-center study. The women were seen at one hospital in Beijing during a short time window.

The sample was enough to detect trends but not large enough to settle every question. We don't know how long these antibodies persisted or whether they stayed positive on repeat testing — a standard requirement for a true antiphospholipid syndrome diagnosis.

Different COVID variants may also trigger different immune responses, and this study came from a specific wave.

Larger multi-center studies are needed to confirm the numbers and see if routine post-COVID screening improves outcomes.

Trials could also explore whether any treatments — such as low-dose aspirin, already common in high-risk pregnancies — help women who test positive after a COVID infection. Until that evidence exists, care should be individualized with a trusted obstetric team.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
To investigate the prevalence of antiphospholipid antibodies (aPLs) in pregnant women infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and their impact on maternal-fetal outcomes, with an emphasis on gestational stage-specific differences and lupus anticoagulant (LAC) positivity. This prospective, observational cohort study was conducted at the Department of Obstetrics, Peking University People’s Hospital, from December 2022 to January 2023. Eligible participants were singleton pregnant women without pre-existing pregnancy complications who tested positive for SARS-CoV-2. Serum samples were collected 2–4 weeks post-infection for testing of aPLs, including LAC, anti-β2-glycoprotein I (aβ2GPI), and anticardiolipin antibodies. Maternal and fetal outcomes were monitored according to standard prenatal care protocols, with specific attention to placental dysfunction related complications. The overall prevalence of aPLs in pregnant women infected with SARS-CoV-2 was 18.75%. All positive cases were single-antibody positive, either for aβ2GPI or LAC, with no instances of multiple antibody co-positivity. The prevalence of aPLs was significantly correlated with the gestational stage at the time of infection, rising from 5.88% in the first trimester to 16.00% in the second trimester and 26.31% in the third trimester (P SARS-CoV-2 infection during pregnancy significantly increases the prevalence of aPLs, with a pattern that is dependent on the gestational stage. Positivity for aPLs, particularly LAC, is an independent risk factor for complications related to placental dysfunction. Our findings suggest that pregnant women infected with SARS-CoV-2, especially those in the third trimester, should undergo aPLs screening 2–4 weeks post-infection, along with enhanced monitoring for placental dysfunction, there should be vigilant surveillance of infection status, coagulation function, and appropriate obstetric management.
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