Maurice Hilleman
Developed over 40 vaccines; saved millions of lives annually.
via Wikipedia: Maurice Hilleman · see source
Maurice Ralph Hilleman (August 30, 1919 – April 11, 2005) was an American microbiologist whose work in vaccinology led to the creation of more than 40 vaccines—a record no one else has matched. Estimates suggest his vaccines prevent about eight million deaths every year. Many consider him the most influential figure in vaccine history, and he is often called the "father of modern vaccines." Robert Gallo described him as "the most successful vaccinologist in history," and some researchers claim he saved more lives than any other scientist of the 20th century.
Of the 14 vaccines routinely recommended in the United States, Hilleman and his team developed eight: those for measles, mumps, hepatitis A, hepatitis B, chickenpox, *Neisseria meningitidis*, *Streptococcus pneumoniae*, and *Haemophilus influenzae*. During a flu pandemic that began in Southern China, his vaccine is thought to have saved hundreds of thousands of lives. He also helped create the vaccine for the Hong Kong flu and contributed to the discovery of antigenic shift and drift, the cold-causing adenoviruses, the hepatitis viruses, and the potentially cancer-linked SV40 virus.
Hilleman was born on a farm near Miles City, Montana, the eighth child of Anna and Gustav Hillemann. His twin sister died the day they were born, and his mother died two days later. He was raised by his uncle Bob Hilleman and worked on the family farm as a boy. He later credited his success to his early experience with chickens, as fertile chicken eggs had been used since the 1930s to grow viruses for vaccines. His family belonged to the Lutheran Church–Missouri Synod. In eighth grade, he discovered Charles Darwin and was caught reading *On the Origin of Species* in church; he later rejected religion. He nearly missed college due to lack of funds, but his eldest brother stepped in. With family help and scholarships, Hilleman graduated first in his class from Montana State University in 1941. He then won a fellowship to the University of Chicago, earning his doctorate in microbiology in 1944. His thesis focused on chlamydia infections, then thought to be viral; he proved they were caused by the bacterium *Chlamydia trachomatis*, which grows only inside cells.
After joining E.R. Squibb & Sons (now Bristol-Myers Squibb), Hilleman developed a vaccine against Japanese B encephalitis, which threatened U.S. troops in the Pacific during World War II. As chief of the Department of Respiratory Diseases at the Army Medical Center (now Walter Reed Army Institute of Research) from 1948 to 1957, he discovered the genetic changes in the influenza virus known as antigenic shift and drift, theorizing that yearly flu shots would be necessary. In 1957, he moved to Merck & Co. in Rahway, New Jersey, as head of its new virus and cell biology research department in West Point, Pennsylvania. There he developed most of his 40 vaccines, working at the lab bench and providing scientific leadership. He also served on many national and international advisory boards, including the NIH's Office of AIDS Research Program Evaluation and the Advisory Committee on Immunization Practices.
In 1957, Hilleman was among the first to realize that a flu outbreak in Hong Kong could become a massive pandemic. After nine 14-hour days, he and a colleague identified it as a new, deadly strain. Forty million vaccine doses were prepared and distributed. Though 69,000 Americans died, the death toll could have been far higher. He received the Distinguished Service Medal from the U.S. military for his work. His vaccine is believed to have saved hundreds of thousands of lives. During the 1968 Hong Kong flu pandemic, he and his team again played a key role, making nine million doses available in four months.
Hilleman was an early voice warning that simian viruses might contaminate vaccines. The most famous of these is SV40, which contaminated some polio vaccines produced from 1955 to 1963, including both Salk's inactivated and Sabin's oral live vaccines.
In 1963, his daughter Jeryl Lynn came down with the mumps. Hilleman took material from her and used it to create a mumps vaccine. The Jeryl Lynn strain is still used today, including in the trivalent MMR vaccine (measles, mumps, rubella) he also developed—the first approved vaccine combining multiple live virus strains. Like many vaccines of that era, it was tested on children with intellectual disabilities living in group homes, because their crowded conditions put them at higher risk for infectious disease.
Hilleman and his team invented a hepatitis B vaccine by treating blood serum with pepsin, urea, and formaldehyde. Licensed in 1981, it was withdrawn in the United States in 1986 and replaced by a vaccine produced in yeast, which is still in use. By 2003, 150 countries were using it, and the incidence of the disease had dropped dramatically.
- born
- August 30, 1919
- died
- April 11, 2005
- field
- Microbiology, vaccinology
- nationality
- American
- known_for
- Developing over 40 vaccines, including eight in routine American schedules; disc
Verified Timeline
Lore & Background
Hilleman was born on a farm near the high plains town of Miles City, Montana. His parents were Anna (Uelsmann) and Gustav Hillemann, and he was their eighth child. His twin sister died on the day the twins were born, and his mother died two days later. He was raised in the nearby household of his uncle, Bob Hilleman, and worked in his youth on the family farm. He credited much of his success to his work with chickens as a boy. His family belonged to the Lutheran Church–Missouri Synod. When he was in the eighth grade, he discovered Charles Darwin, and was caught reading On the Origin of Species in church. Later in life, he rejected religion. Due to lack of funds, he almost failed to attend college. His eldest brother interceded, and Hilleman graduated first in his class in 1941 from Montana State University with family help and scholarships. He won a fellowship to the University of Chicago and received his doctoral degree in microbiology in 1944. His doctoral thesis was on chlamydia infections, which were then thought to be caused by a virus. Hilleman showed that these infections were actually caused by a species of bacterium, Chlamydia trachomatis, that grows only inside of cells.
Reader's Guide
Hilleman's significance lies in his unmatched productivity in vaccine development, which has had a profound global impact on public health. His vaccines, including those for measles, mumps, hepatitis B, and several bacterial diseases, are estimated to save nearly eight million lives each year. He was among the first to recognize that a 1957 outbreak of influenza in Hong Kong could become a huge pandemic. Working on a hunch, after nine 14-hour days he and a colleague determined that it was a new strain of flu that could kill millions. Forty million doses of vaccines were prepared and distributed. Although 69,000 Americans died, the pandemic could have resulted in many more deaths in the United States. His vaccine is believed to have saved hundreds of thousands of lives. In 1963, his daughter Jeryl Lynn came down with the mumps. He cultivated material from her, and used it as the basis of a mumps vaccine. The Jeryl Lynn strain of the mumps vaccine is still used. He and his group invented a vaccine for hepatitis B by treating blood serum with pepsin, urea and formaldehyde. This was licensed in 1981, but withdrawn in 1986 in the United States and replaced by a vaccine that was produced in yeast. By 2003, 150 countries were using it and the incidence of the disease in the United States in young people had decreased by 95%. Hilleman considered his work on this vaccine to be his single greatest achievement. Despite his forceful personality and modest claims—none of his vaccines or discoveries are named after him—his contributions have been widely honored, including the National Medal of Science presented by President Ronald Reagan in 1988 and a special lifetime achievement award from the World Health Organization.
Did You Know?
- Hilleman's twin sister died on the day they were born, and his mother died two days later.
- He was caught reading Charles Darwin's On the Origin of Species in church when he was in the eighth grade.
- His mumps vaccine was developed from material taken from his daughter Jeryl Lynn in 1963, and the Jeryl Lynn strain is still used today.
- He kept a row of fake 'shrunken heads' in his office as trophies representing each of his fired employees.
- Robert Gallo called Hilleman 'the most successful vaccinologist in history.'
Frequently Asked Questions
Who is Maurice Hilleman?
Maurice Ralph Hilleman (1919–2005) was an American microbiologist and vaccinologist whose career centered on designing disease-preventing vaccines. He is widely regarded as one of the most productive and influential figures in the history of immunology.
How many vaccines did Maurice Hilleman develop?
Hilleman and his team created more than forty vaccines over the course of his career. Eight of those—covering measles, mumps, hepatitis A and B, chickenpox, meningococcal disease, pneumococcal disease, and Haemophilus infections—appear on the standard U.S. immunization schedule.
Why is Maurice Hilleman called the 'father of modern vaccines'?
The nickname reflects his extraordinary output and the sheer number of routine childhood vaccines he personally helped bring to market. His work spanned decades of discovery, from identifying antigenic shift and drift to formulating vaccines against viruses and bacteria that previously had no preventive treatment.
How did Maurice Hilleman create the mumps vaccine?
The mumps vaccine originated from a virus strain he isolated from his own daughter, who had contracted the illness. He then worked to attenuate that strain into a safe, effective vaccine that became part of the combined MMR shot.
What is the estimated impact of Maurice Hilleman's vaccines on global health?
One commonly cited estimate suggests his vaccines prevent roughly eight million deaths every year worldwide. That figure underscores why he is often described as one of the most consequential public-health scientists of the twentieth century.
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