Several decades after William
Harvey demonstrated the circulation of blood, early attempts at blood
transfusion began. In 1665, Richard Lower successfully kept dogs alive by
transfusing blood from other dogs. Two years later, Jean-Baptiste Denys
conducted the first documented blood transfusion in a human subject. While some
single transfusions proved successful, recipients often experienced severe
complications after their second or third transfusion. By the end of the
seventeenth century, blood transfusions were banned and faded into obscurity
until 1818, when English obstetrician James Blundell performed the first
successful human blood transfusion to treat postpartum bleeding. Between 1825
and 1830, he carried out ten transfusions, five of which yielded positive
results. Blundell not only achieved medical success but also gained financial
reward, earning an equivalent of approximately $50 million today from his
invention of blood transfusion instruments.
The discovery of blood types
by Austrian-born American immunologist Karl Landsteiner revolutionized blood
transfusions, making them a routine medical procedure. In 1901, while at
Vienna’s Institute of Pathology, Landsteiner found that the blood of some
individuals could agglutinate (clump) with the blood of others, leading to
potentially fatal reactions due to an immunological (antigen-antibody)
response. He identified three human blood groups: A, B, and C (which was later
renamed O), and later discovered a fourth group, AB.
Landsteiner's blood typing
laid the groundwork for the first successful transfusions of compatible blood,
conducted in 1907 at Mt. Sinai Hospital in New York, and later on a large scale
during World War I. By 1927, ABO blood types were being utilized in paternity
suits to determine the biological parents of children. For his groundbreaking
discovery of human blood groups and the ABO blood typing system, Landsteiner
was awarded the Nobel Prize in 1930. In 1940, while working at the Rockefeller
Institute (now Rockefeller University), he identified the Rh factor in Rhesus
monkeys, which was linked to hemolytic disease of the newborn—a potentially
life-threatening condition occurring when a mother and her fetus have
incompatible blood types.
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