Antibodies
derived from an ebola survivor to cure seriously-ill patients. This is what US Dr James Crow, from the Vanderbildt University tries to achieve together
with pharmaceutical company Mapp. This is the producer of the experimental
ebola drug ZMapp, consisting
of a cocktail of three antibodies originating from mice. Human derived antibodies could be better in beating
the virus
From DNA to antibody
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhkrI5gDgH4OJYZjaBhVv6SpGKfMDSKwLbqIWdPTvv_ESh6ohI7EEB_SHeW4gnqn0bh6EvmBaeDvg58U28Rmdn3nm6N2b-Bp3KPsxdS9SAno7nb1jxxN9ir_ogGEUv_kw4I2bt04kBs2Io3/s1600/ebola+transport.jpg)
Cloning
antibodies from patients is a well-known method. But why should you clone them, why not purify
them directly from the blood? That is because large volumes of patient blood are
needed to purify sufficient amounts of antibodies. During the height of the epidemic
many patients have high titers of anti-ebola antibodies. But when the disease
fades out, the titers drop. Complicating factor is that many patients are
infected with other viruses or parasites, like HIV. You don’t want that
in your medication vial.
Purified from blood
Nevertheless,
this is frequently done. Think of tetanus. For this disease in the Netherlands
volunteer donors are frequently vaccinated to maintain high titers. The antibodies
are purified from their blood to cure patients who have contacted this serious
disease. The same goes for anti-rhesus-D injections. Antibodies to rhesus D are
purified from blood of women who in the past had made antibodies to their babies.
Next, patients with immune deficiencies receive antibodies
purified from plasma of thousands of blood bank donors. They get the entire
spectrum, so to defeat all general occurring infections.
The
question remains whether Sacra survived thanks to his effective antibodies or
whether the supporting treatment in an US hospital was crucial.
Source: http://www.reuters.com/article/2014/12/22/us-health-ebola-usa-antibodies-exclusive-idUSKBN0K00VA20141222
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