Henrietta Lacks
Henrietta Lacks was an American woman whose cervical cancer cells were used to create the HeLa cell line, the first widely known immortal human cell line.
Henrietta Lacks was an American woman whose cervical cancer cells were used to create the HeLa cell line, the first widely known immortal human cell line. Her cells became central to major advances in biomedical research, while her case also became a landmark example in debates over consent, ethics, and the use of human tissue in research. Lacks died at age 31 in Baltimore in 1951.
Early life
Henrietta Lacks was born Loretta Pleasant in Roanoke, Virginia, and later lived in rural Virginia before moving with family near Baltimore. She was an African-American tobacco farmer and mother of five.
HeLa cells
During treatment for cervical cancer at Johns Hopkins Hospital in 1951, cells from Lacks’s tumour were cultured and became the HeLa cell line. The line proved unusually robust and is described as the first immortal human cell line, becoming one of the most important tools in biomedical research.
Scientific impact
HeLa cells have been used in research on cancer, viruses, genetics, vaccines, and many other areas of medicine. They contributed to advances including the polio vaccine, cancer research, virology, and genetics, and remain widely used in laboratories.
Ethics and legacy
Lacks’s case raised major questions about informed consent, ownership of human tissue, and the treatment of Black patients in medical research. Her cells were taken without her knowledge or consent, and her story has been the subject of books, documentaries, public memorials, and institutional recognition.
Key facts
- Lacks’s cervical cancer cells were taken during treatment in 1951 and later used to establish the HeLa cell line.
- HeLa is described as the first immortal human cell line and has been used widely in biomedical research.
- Her cells contributed to advances including the polio vaccine, cancer research, virology, and genetics.
- Her case became central to public discussion of informed consent and patient rights in medical research.
- Lacks died at age 31 in Baltimore in 1951.
Henrietta Lacks is relevant to Canadian readers because her story is widely discussed in medical ethics, biomedical research, and patient-consent debates in Canada, where the HeLa case is often used in teaching and policy discussions.
Frequently asked questions
Who was Henrietta Lacks?
What are HeLa cells?
Why is Henrietta Lacks important?
Did Henrietta Lacks know her cells were used for research?
What did HeLa cells help develop?
References
- Encyclopaedia Britannica — https://www.britannica.com/biography/Henrietta-LacksSupports: Birth, death, identity, and HeLa cell line significance.
- PubMed Central / NIH — https://pmc.ncbi.nlm.nih.gov/articles/PMC3516052/Supports: Biographical background and origin of the HeLa cell line.
- World Health Organization — https://www.who.int/news/item/13-10-2021-who-director-general-bestows-posthumous-award-on-the-late-henrietta-lacksSupports: Consent issues, scientific impact, and posthumous recognition.
- Johns Hopkins Medicine — https://www.hopkinsmedicine.org/henrietta-lacksSupports: HeLa legacy and research uses.
- National Human Genome Research Institute — https://www.genome.gov/sites/default/files/media/files/2019-07/hela_timeline.pdfSupports: Tissue use without consent and scientific impact of HeLa cells.
- Maryland State Archives — https://msa.maryland.gov/msa/educ/exhibits/womenshallfame/html/lacks.htmlSupports: Birth name, birthplace, death, and HeLa naming.