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Jonas Edward Salk (October 28, 1914 - June 23, 1995) was an American physician and researcher best known for the development of the first successful polio vaccine (the eponymous Salk vaccine).
During his life he worked in New York, Michigan, Pittsburgh and California. In his later career, Salk devoted much energy toward the development of an AIDS vaccine.
Salk did not seek wealth or fame through his innovations, famously stating, "Who owns my polio vaccine? The people! Could you patent the sun?"
Salk was born in New York City to poor Russian-Jewish immigrant parents, Doran and Daniel B. Salk. He graduated from Townsend Harris High School and then went to the City College of New York, where he earned a B.Sc.. He received a medical degree from the College of Medicine at New York University in June 1939.
While in college he met his future wife, Donna Lindsay, whom he married on June 9, 1939. They had three children: Peter, Darrell, and Jonathan. In 1968, they divorced, and in 1970 Salk married Françoise Gilot, the former mistress of Pablo Picasso.
After medical school, Salk first worked as a staff physician at the Mount Sinai School of Medicine in New York City. Later, he worked for Dr. Tommy Francis's virus lab at the University of Michigan in Ann Arbor. In 1947, he moved to Pittsburgh, where he led the Virus Research lab at the University of Pittsburgh. During the 1950s, he developed, tested, and refined the first successful polio vaccine. In 1955 he began immunizations at Pittsburgh's Arsenal Elementary School in the Lawrenceville neighborhood and made international news as the man who beat polio.
In 1965, Salk struck out on his own, leaving the University of Pittsburgh and establishing the Salk Institute for Biological Studies in La Jolla, California, where the major focus of study was molecular biology and genetics. The first faculty included many distinguished members such as Jacob Bronowski and Francis Crick. Salk directed the institute until his retirement in 1985.
During his life, he received many awards and honors: The Lasker Award (1956), The Bruce Memorial Award (1958), The Jawaharlal Nehru Award (1975), Congressional Gold Medal and Presidential Medal of Freedom (1977).
As a child, Salk did not show any interest in medicine or science in general. He says in an interview with the Academy of Achievement:
As a child I was not interested in science. I was merely interested in things human, the human side of nature, if you like, and I continue to be interested in that. That's what motivates me. And in a way, it's the human dimension that has intrigued me.
His first desire was to become a lawyer and only due to his mother's persuasion (which included her telling him he wouldn't be good at it), he changed from a pre-law student to a pre-med student. During his first year in medical school, he was offered the chance to do research and teach biochemistry. He recalls this experience in the previously mentioned interview:
At one point at the end of my first year of medical school, I received an opportunity to spend a year in research and teaching in biochemistry, which I did. And at the end of that year, I was told I could, if I wished, switch and get a Ph.D. in biochemistry but my preference was to stay with medicine. And I believe that this is all linked to my original ambition, or desire, which was to be of some help to humankind, so to speak, in a larger sense than just on a one-to-one basis.
While attending NY Medical College, he heard two lectures that would change his life forever. Salk reflected on the lectures in 1990:
In the first lecture, we were told that it was possible to immunize against diphtheria and tetanus by the use of a chemically treated toxin [to kill it]... In the very next lecture, we were told that in order to immunize against a virus disease it was necessary to go through the experience of infection. It was not possible to kill the virus... The light went on at that point. I said that those two statements can't possibly both be true. One has to be false.
In 1938, while still at the college, Salk began working with Dr. Thomas Francis, Jr. on an influenza vaccine. In 1941, Francis was appointed the head of the epidemiology department at the newly formed School of Public Health at the University of Michigan, and Salk, who in 1942 won a research fellowship, followed him. Together they worked to develop an influenza vaccine at the behest of the U.S. Army. Salk advanced to the position of assistant professor of epidemiology and continued his work on virology.
In 1947, Salk received a position at the University of Pittsburgh, as the head of the Virus Research lab. Though he continued his research on improving the influenza vaccine, he set his sights on the poliomyelitis virus. The poliovirus initially attacks the nervous system and within a few hours of infection, paralysis can occur. The death rate of the disease is about 5-10%. Death usually occurs when the breathing muscles become paralyzed. Polio was sometimes hard to diagnose because of its flu-like symptoms, which include stiff neck, fever, and headache.
At that time, it was believed that immunity can come only after the body has survived at least a mild infection by live virus. In contrast, Salk observed that it is possible to acquire immunity through contact with inactivated (killed) virus. Using formaldehyde, Salk killed the poliovirus, but kept it intact enough to trigger the necessary immune response. Salk's research caught the attention of Basil O'Connor, president of the National Foundation for Infantile Paralysis (now known as the March of Dimes Birth Defects Foundation). The organization decided to fund Salk's efforts to develop a killed virus vaccine.
The vaccine was first tested in monkeys, and then in patients at the D.T. Watson Home for Crippled Children. After successful tests, in 1952, Salk tested his vaccine on volunteering parties, including himself, the laboratory staff, his wife, and his children. In 1954, national testing began on two million children, ages six to nine, who became known as the Polio Pioneers. This was one of the first double-blind placebo-controlled tests, which has since become standard: half of the treated received the vaccine, and half received a placebo, where neither the individuals nor the researchers know who belongs to the control group and the experimental group. One-third of the children, who lived in areas where vaccine was not available, were observed in order to evaluate the background level of polio in this age group. On April 12, 1955, the results were announced: the vaccine was safe and effective. The patient would develop immunity to the live disease due to the body's earlier reaction to the killed virus.
Salk's vaccine was instrumental in beginning the eradication of polio, a once widely-feared disease. Polio's outbreak in 1916 left 6000 dead and 27,000 paralyzed. In 1952, 57,628 cases were recorded. After the vaccine became available, polio cases in the U.S. dropped by 85-90 percent in only two years.
However, the live-virus oral vaccine developed by Albert Sabin became the preferred alternative after a sometimes intense clash between the two scientists and their adherents. The Salk vaccine, which is injected, proved to be effective in sharply reducing the number of polio cases in the United States. But the Sabin vaccine had the advantage of easier delivery and became accepted in the United States after the testing abroad. It was licensed in 1961 and eventually became the vaccine of choice in most parts of the world. The last indigenous case of polio in the U.S. was reported in 1991. Partly because of that fact, only inactivated, Salk-type polio vaccines have been recommended for use in the United States since 2000.
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