The Black Woman Behind the World's Most Groundbreaking Medical Research

Henrietta was just 31 years old when she died from cervical cancer in 1951, but many medical researchers consider her immortal. At the time of her death, her family didn’t know that Henrietta would be the catalyst for breakthroughs in cancer, polio, cloning, and gene mapping, among other things. That’s because the doctors who took Henrietta’s cells did so without her or her family’s authorization.

“My mother would be so proud that her cells saved lives,” Henrietta’s son, Lawrence Lacks, said in a statement. “She’d be horrified that Johns Hopkins profited while her family to this day has no rights.”

In a 2010 statement, the hospital said:
“Johns Hopkins Medicine sincerely acknowledges the contribution to advances in biomedical research made possible by Henrietta Lacks and HeLa cells. It’s important to note that at the time the cells were taken from Mrs. Lacks’ tissue, the practice of obtaining informed consent from cell or tissue donors was essentially unknown among academic medical centers […] The laboratory that received Mrs. Lacks’s cells had arranged many years earlier to obtain such cells from any patient diagnosed with cervical cancer as a way to learn more about a serious disease that took the lives of so many.”

HeLa cells were the first known cells to live outside of the body, which is why they’ve been dubbed “immortal” by many. Some of the cells were healthy, while others were cancerous. But somehow they became the most used cells in medical scientific research.

The polio vaccine, in vitro fertilization, and numerous cancer treatments have all been pioneered in whole or in part through the use of HeLa cells. The cells, which continue to grow and flourish outside of the body, allow for uniformity in research and an unlimited availability of cells.

The controversy surrounding the way in which Henrietta’s cells were obtained is still ongoing. In 2013, the Lacks family reached an agreement that researchers needed permission from the National Institutes of Health (NIH) to use HeLa cells. And just this month, the Lacks family requested compensation for the use of Henrietta’s cells.

“Everyone else is making funds off Henrietta’s cells,” Henrietta’s grandson Ron Lacks said, according to the Washington Post. “I am sure my grandmother is up in heaven saying, ‘Well, what about my family?’ ”
Henrietta’s story is set to be the subject of an HBO movie based on the 2010 book, The Immortal Life of Henrietta Lacks by Rebecca Skloot. The movie, which stars Oprah Winfrey, is set to premiere on April 22nd this year.