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When it comes to creating treatments for Covid-19, the disease caused by the novel coronavirus, the first line of defense may be a century-old technology: purified blood plasma.

Medical literature published during the Spanish flu pandemic of 1918 includes case reports describing how transfusions of blood products obtained from survivors may have contributed to a 50% reduction in death among severely ill patients. In 1934, a measles outbreak at a Pennsylvania boarding school was halted when serum harvested from the first infected student was used to treat 62 fellow students. Only three of the 62 students developed measles — all mild cases.

More recently, plasma-derived therapy was used to treat patients during outbreaks of Ebola and avian flu. And on Wednesday the Japanese drugmaker Takeda Pharmaceutical Co. said it was developing a new coronavirus drug derived from the blood plasma of people who have recovered from Covid-19. Its approach is based on the idea that antibodies developed by recovered patients might strengthen the immune system of new patients.


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Here’s what you need to know about how this old technology might help slow the coronavirus outbreak.

How is blood plasma turned into an infection-fighting drug?

Patients who have recovered from a disease have permanent antibodies generated by the immune system floating in their blood plasma, the liquid component of blood. To turn that into a drug, the plasma is harvested, tested for safety, and purified to isolate those protective antibodies. When injected into a new patient, the “plasma-derived therapy” — also known as convalescent plasma — provides “passive immunity” until the patient’s immune system can generate its own antibodies.


Mike Ryan, the head of the WHO’s emergencies program, has said convalescent plasma is a “very important area to pursue” as a potential treatment for patients with Covid-19. “It must be given at the right time because it mops up the virus in the system and it just gives the new patient’s immune system a vital push at the time it needs it — but it has to be carefully time and it’s not always successful.”

Is this approach already being used in this outbreak?

In February, doctors in Shanghai set up a special clinical to administer convalescent plasma to select patients who were newly infected with coronavirus.

“In China, we’ve only heard anecdotal reports of encouraging results. Nothing has been published yet,” said Greg Poland, a physician and infectious disease expert at the Mayo Clinic in Rochester, Minn. “But this approach is definitely worth trying.”

How is what Takeda is doing different?

Takeda already makes a medicine called intravenous immunoglobin, or IVIG, for treating patients who have immune disorders. It consists of antibodies of all types purified from the blood plasma of healthy people. Giving antibodies in this purified form is easier, because it requires a much lower volume of treatment; it’s safer, because there is no chance of transmitting other viruses; and it’s more efficient.

With its new treatment, TAK-888, Takeda hopes to create an IVIG from the blood of people who have been infected with the coronavirus and who have recovered. That could create a treatment or prophylactic relatively quickly. It might not need to go through phase I studies to demonstrate basic safety, or larger phase III studies to demonstrate efficacy. That means the treatment could be available sooner.

The other advantage of this approach is that researchers don’t need to figure out which antibodies work best at fighting off the novel coronavirus. They basically import the entire disease-fighting army of antibodies from patients whose bodies have already won. The antibodies in TAK-888 will be more narrowly selected to target coronavirus than those in garden variety IVIG.

How much of this new drug can Takeda make?

“We are not looking at this as a therapy that everyone should go on,” Julie Kim, the president of Takeda’s blood plasma unit, told STAT. “This will be targeted to patients who have severe disease.”

Kim said the hope is that a single donor might provide enough IVIG for a single patient. But it’s also possible that IVIG derived from several people would be needed to treat each patient. Takeda won’t know until it has taken steps to learn how many antibodies are present in patients who have recovered, and what dose of TAK-888 appears necessary to be effective. Those measures, Takeda said, could be discovered without large-scale trials.

Kim said that she could not comment on precise timelines until Takeda has had discussions with regulators like the Food and Drug Administration.

Are there others working with antibody treatments?

Yes. Among them is Regeneron, which is working on a mix of manufactured antibodies to attack the coronavirus. Vir Biotechnology, another biotech firm, has said it will have a similar approach.

The IVIG approach Takeda is using is known as “polyclonal antibodies,” which means, simply, that there are a lot of different types of antibodies in the mix. But many biotech drugs are what are known as monoclonal antibodies, single antibodies that can be originally generated in mice and then manufactured in huge tanks of cells.

One reason to be optimistic is that Regeneron has pulled it off before, manufacturing a treatment composed of three different monoclonal antibodies that appears to have some effectiveness against the Ebola virus.

Geoffrey Porges, an analyst at the investment bank SVB Leerink, said in an interview he was “very impressed” with the speed at which Regeneron developed an Ebola treatment. He said that the novel coronavirus might be harder, because it is not clear what parts of the rapidly mutating virus antibodies should target. “But if anyone can figure this out, it’s Regeneron,” he said.

Don’t vaccines also work by creating antibodies?

Vaccines work by teaching the body to make its own antibodies to an infectious agent without a person ever becoming infected. This is why they are among the most powerful weapons in public health.

But Porges, who worked at Merck’s vaccine division in the 1990s, said he thinks that creating a vaccine might be harder than companies expect, because this new virus is just not well enough understood. “You kind of need to have some fundamental understanding of the immunology and the virus before you can develop a vaccine,” he said. “It’s not clear to me that we have that.”

Many companies, including the biotechnology firm Moderna and the large pharmaceutical companies Johnson & Johnson and Sanofi, are working hard to develop vaccines quickly.

So which of these approaches is better? 

That’s not the right question. Convalescent plasma, and then IVIG, could provide our first-line defense for people with Covid-19, especially those who are older and at much higher risk for complications. A monoclonal antibody drug could reach a greater number of patients. We also need antiviral drugs, such as remdesivir, being tested by Gilead Sciences. And a vaccine could do the most to slow or stop transmission.

“We need them all,” said Poland of the Mayo Clinic.

Andrew Joseph contributed reporting.

  • On behalf of those people affected with the coronavirus and the entire world, i would like to join hands and wish all of them quick recovery

  • Does coronavirus seem to be affecting a specific blood type?meaning more one blood type than another??

  • Answering my wife’s question: How are they going to treat Corona virus patients, as an anthropologist with some epidemiological training I remembered impressive anecdotal information from the Ebola crisis that there were survivors with immunity that were doing heroic contact work that other health workers could never do without “spacesuit” protection. Rushing to my computer, as I explained, I said that this might be the best course for a Covid-19 solution. I plugged it into Google and was very pleased to find that this approach was already in the works.
    I imagine that scientific work may have been done on the ebola survivor’s activity, if so it could be a resource for further development of this very promising approach–as is the historical info from the Spanish flu and even more so from the 1934 Measles treatment. This approach is so promising, with already significant numbers of survivor resources available, NOW would be THE time to launch an “All hands on Deck” collective effort to pool all the relevant researchers [mentioned above] to put their work together to defeat this global threat before it is too late.

  • Excellent concept. This actually will work. Has worked by pooling blood plasma for replacing passive immunity in animals that are unable to receive colostrum from there dam.

  • I am on IG medication (but in subcutaneous form, not IV). I’ve been on plasma-based medicine made by the plasma company Takeda bought (Shire) and another company’s medication because I have a genetic immunodeficiency. It takes dozens of donors at plasma centers to make one dose of my medication. Further, how would you encourage people who survived COVID-19 to donate plasma? Right now they pay donors. They also have to meet rigorous health and age requirements to donate. It’s a great concept but how could they execute this on a large scale? I’m skeptical.

    • It is sad to think that Human compassion without compensation is what matters. I whould recommend that Interferon is considered in your course of treatment. Wishing you the best in your recovery.👍

    • Can’t speak for everyone but if I were infected and sucking some of my blood could help save someone else’s loved one I’d happily do it. No money required.

      People donate to the blood bank all the time. Why would this be any different?

  • Both approaches are good. I suggest a third drug: Monoclonal humanized IgA with secretory factor nebulized. See if any researchers would consider this.

  • Is there enough research on if certain blood types are more susceptible to catching the virus?

    • Alicia Gonzales, that is exactly what I’m looking for too. Does it affect all blood types equally, or is any type immune to it?

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