Blood type is a minor player in a much larger cast
Harvard and Emory researchers found coronavirus shows strong preference for binding to proteins unique to blood type A, particularly in lung cells. Multiple studies worldwide show conflicting results; some confirm type A vulnerability while others find no correlation between blood type and disease severity.
- Harvard and Emory researchers found the coronavirus shows strong preference for binding to type A blood antigens in lung cells
- A Brazilian study found type A patients had 2.5 times greater severity risk compared to type O
- Multiple international studies produced conflicting results; no scientific consensus exists on blood type's role in COVID-19 severity
- Type A blood shows greater clotting activity than type O, potentially explaining increased thrombosis risk in severe COVID cases
Research suggests blood type A may increase COVID-19 severity risk while type O offers protection, but scientists warn findings remain preliminary with no scientific consensus on the association.
When the pandemic was still new, Chinese researchers published preliminary findings suggesting that people with blood type A faced higher infection risk from the coronavirus, while those with type O seemed protected. The observation sparked dozens of investigations worldwide, each trying to answer a deceptively simple question: Does the virus care what blood type you are?
The question matters because blood type has been shown to influence vulnerability to other diseases—malaria, hepatitis B, HIV, and bacterial infections have all demonstrated associations with ABO groups. When researchers at Harvard and Emory examined the coronavirus at the molecular level, they found something striking. The virus showed what they called a "strong preference" for binding to proteins present only on type A blood cells, particularly those lining the lungs. The study, published in Blood Advances in March 2021, offered what appeared to be direct evidence of a biological mechanism linking blood type to disease risk.
But the scientific picture fractured almost immediately. A Boston hospital study published months earlier found that types B and AB carried higher infection risk, while type O showed protection—yet type A appeared statistically neutral. A Danish study of over two million people confirmed type O's protective effect against infection but found blood type irrelevant to hospitalization or death. Other investigations produced still different results. Scientists interviewed by the BBC cautioned that these preliminary findings should not trigger alarm or carelessness with preventive measures. The variation, they explained, reflected the messy reality of how science actually works: researchers using different methods, studying different populations, wrestling with confounding factors that blur the picture.
In Brazil, researchers stumbled onto their own evidence almost by accident. Gil de Santis, a blood specialist at a São Paulo teaching hospital, noticed something odd while running a clinical trial on convalescent plasma treatment. His team had to type patients' blood before transfusing them, and he kept seeing far more type A patients among the severely ill than the local population would predict. When his group compared 72 severe COVID patients against 160 controls from the same region, type A appeared in 51 percent of the sick versus 30 percent of the healthy. Type O showed the inverse pattern. The math suggested type A carried 2.5 times greater risk of severe disease. Yet Santis was careful to contextualize the finding: coronary disease increased severity risk twentyfold, diabetes five to sevenfold. Blood type, he emphasized, was a minor player in a much larger cast.
Other Brazilian teams reported similar patterns. In Rio Grande do Sul, a blood bank noticed they were transfusing more type A blood to critically ill COVID patients than their usual demand would suggest—47 percent versus their normal 35 percent. In Goiás, however, researchers analyzing plasma donors found type O most common among those who had recovered, with type A second, matching the general population distribution. When they looked at severe cases, they found type AB predominant and type A nearly absent—contradicting the other studies entirely. The hematologist leading that work, Maria Amorelli, noted that the sample was small and donor populations skew toward type O because of a widespread belief that it is the universal donor. She advised against panic: many type A patients had mild disease, many type O patients had severe cases.
The biological mechanisms proposed to explain any connection remain speculative. Type A blood carries the A antigen, a protein on cell surfaces that the virus appears to favor. But blood type also determines which natural antibodies a person carries—type A individuals have anti-B antibodies, type O individuals have both anti-A and anti-B. Some researchers hypothesize these antibodies might offer protection against viral entry. A third factor emerged in the research: type A blood tends toward greater clotting activity, and severe COVID frequently triggers dangerous blood clots. Type O blood shows less clotting tendency, potentially offering another protective mechanism.
Sean Stowell, one of the Harvard researchers, acknowledged in correspondence with the BBC that the ideal study to settle the question would be impossible to conduct ethically. A truly definitive experiment would require deliberately exposing people with different blood types to equal amounts of virus—something no review board would ever approve. Researchers are therefore left with correlational studies and laboratory experiments, each with inherent limitations. New variants of the virus, Stowell noted, would require new investigation. The science has not reached consensus, and may never reach certainty. For now, having type A blood is not a reason for despair, and having type O is not a reason for complacency.
Citas Notables
Blood type is not something we investigate upfront to assess whether a patient will have more or less risk. Findings have not been relevant enough to change our clinical behavior.— Maria Amorelli, hematologist at Goiás blood bank
A prospective study with equal viral exposure would be necessary to answer this definitively, but such a study would be completely unethical and will never be conducted.— Sean Stowell, Harvard researcher
La Conversación del Hearth Otra perspectiva de la historia
Why did this question about blood type even emerge? It seems oddly specific.
Because early in the pandemic, Chinese researchers noticed that among infected patients in Wuhan and Shenzhen, type A appeared more frequently than it did in the general population, while type O appeared less. That observation triggered a cascade of follow-up studies.
And those follow-up studies all confirmed it?
No. Some did, some didn't. A Boston hospital found type B and AB at higher risk. A Danish study confirmed type O's protection but found it didn't matter for severe outcomes. A Brazilian blood bank found type AB most common among the critically ill. The results scattered in different directions.
So why the disagreement? Are the researchers using different methods?
Partly, yes. Different populations, different study designs, different ways of measuring severity. But also, blood type is probably not the main driver of outcomes. Comorbidities—heart disease, diabetes—matter far more. When you're looking for a small effect in a noisy system, you find different things depending on where you look.
But the Harvard study found a direct biological mechanism, right? The virus prefers type A proteins?
It did find that in the lab. The virus binds more readily to type A antigens on lung cells. That's real. But binding preference in a petri dish doesn't necessarily translate to clinical risk in a living person with an immune system, other health conditions, and countless other variables.
So what should someone with type A blood actually do differently?
Nothing. That's what the Brazilian researchers emphasized. Type A patients have had mild cases. Type O patients have had severe ones. Blood type is one variable among dozens. The protective measures—vaccination, masking when needed, treating underlying conditions—matter far more than knowing your ABO group.
Will we ever know for certain?
Probably not. The only way to know would be unethical. You'd need to expose people with different blood types to equal viral loads and watch what happens. No ethics board would approve that. So we're left with observation and laboratory work, both of which have limits.