Prior to the twentieth century, blood and its function was poorly understood. In trying to solve the problem of serious blood loss from injuries, doctors tried to inject (transfuse) blood from another person or animal into the injured patient. In some cases, this worked and the patient recovered. In many more cases, however, the blood transfusion actually harmed the patient, often causing death. No one could predict which type of reaction would occur as a result of a blood transfusion. So, by the beginning of the nineteenth century, most European nations had outlawed the practice of blood transfusion.
About 1900 Austrian-American physician Karl Landsteiner (1868-1943) developed an explanation for the phenomenon of blood rejection. Landsteiner found that human blood serum (the liquid portion of blood surrounding the cells) could be divided into four categories, depending on its ability to cause clotting of red blood cells. He gave these groups the names A, B, AB, and 0 based on what type of clotting antigen they had, if any.
In 1940 Landsteiner discovered another of blood factor antigen, known as Rh. This discovery resulted from Landsteiner's studies with Rhesus monkeys. Landsteiner and his colleagues found that when blood from monkeys was injected into rabbits and guinea pigs, it clotted. This was because of the presence of another antigen that the researchers had not classified before. Landsteiner called this antigen the Rh (Rhesus) factor. Researchers also showed that the factor occurs among some, but not all, humans. It is also inherited.
Importance of Rh Factor
The Rh discovery had immediate practical importance because it explained a relatively common medical disorder known as erythroblastosis fetalis. In this condition, an Rh-negative woman who becomes pregnant with an Rh-positive fetus (an unborn child) sometimes develops anti-bodies against the Rh factor in the fetus. This development usually causes no problem during the woman's first pregnancy, since the number of anti-bodies produced tends to be small.
By the time a second pregnancy occurs, the situation has changed. The number of Rh antibodies produced by the mother's body has become large enough to cause destruction of red blood cells in the fetus. This can result in complications such as anemia (a chronic blood condition characterized by lack of energy), jaundice (a condition in which bile pigments build up in the blood and cause skin, eyeballs and urine to take on a sickly yellow tone) or premature birth. Today, this reaction can be controlled by immunizing Rh negative women after their first pregnancy with a drug known as RhoGam.
About 1900 Austrian-American physician Karl Landsteiner (1868-1943) developed an explanation for the phenomenon of blood rejection. Landsteiner found that human blood serum (the liquid portion of blood surrounding the cells) could be divided into four categories, depending on its ability to cause clotting of red blood cells. He gave these groups the names A, B, AB, and 0 based on what type of clotting antigen they had, if any.
In 1940 Landsteiner discovered another of blood factor antigen, known as Rh. This discovery resulted from Landsteiner's studies with Rhesus monkeys. Landsteiner and his colleagues found that when blood from monkeys was injected into rabbits and guinea pigs, it clotted. This was because of the presence of another antigen that the researchers had not classified before. Landsteiner called this antigen the Rh (Rhesus) factor. Researchers also showed that the factor occurs among some, but not all, humans. It is also inherited.
Importance of Rh Factor
The Rh discovery had immediate practical importance because it explained a relatively common medical disorder known as erythroblastosis fetalis. In this condition, an Rh-negative woman who becomes pregnant with an Rh-positive fetus (an unborn child) sometimes develops anti-bodies against the Rh factor in the fetus. This development usually causes no problem during the woman's first pregnancy, since the number of anti-bodies produced tends to be small.
By the time a second pregnancy occurs, the situation has changed. The number of Rh antibodies produced by the mother's body has become large enough to cause destruction of red blood cells in the fetus. This can result in complications such as anemia (a chronic blood condition characterized by lack of energy), jaundice (a condition in which bile pigments build up in the blood and cause skin, eyeballs and urine to take on a sickly yellow tone) or premature birth. Today, this reaction can be controlled by immunizing Rh negative women after their first pregnancy with a drug known as RhoGam.
No comments:
Post a Comment