The Immortal Life of Henrietta Lacks

"There's no way of knowing exactly how many of Henrietta's cells are alive today. One scientist estimates that if you could pile all HeLa cells ever grown onto a scale, they'd weigh more than 50 million metric tons—an inconceivable number, given that an individual cell weighs almost nothing."

A scientific marvel. In 1951, cells taken from Henrietta Lacks, a young African American woman dying of cervical cancer, became the first human cells to survive and thrive in laboratory conditions. These cells, dubbed HeLa, revolutionized medical research and became one of the most important tools in medicine.

A global impact. HeLa cells have been used in countless scientific breakthroughs:

• Development of the polio vaccine

• Cancer and AIDS research

• In vitro fertilization

• Gene mapping

• Effects of radiation and toxic substances

• Space exploration

Despite their immense contribution to science, the story of Henrietta Lacks and her cells remained largely unknown for decades, raising questions about medical ethics, consent, and the intersection of race and medical research in America.

"HeLa cells were one of the most important things that happened to medicine in the last hundred years."

Unintended immortality. Dr. George Gey, a scientist at Johns Hopkins Hospital, discovered that Henrietta's cancer cells continued to grow and divide indefinitely in laboratory conditions, unlike any other human cells before them. This unique property made HeLa cells invaluable for medical research.

Ethical considerations:

• Cells were taken without Henrietta's knowledge or consent

• Her family was not informed about the cells' existence or importance for decades

• Scientists and companies profited from HeLa cells, while the Lacks family remained in poverty

• The widespread use of HeLa cells raised questions about patient privacy and ownership of bodily tissues

The HeLa cell line sparked debates about informed consent, tissue rights, and the commercialization of human biological materials that continue to this day.

"The Lackses were convinced that Hopkins had stolen their mother's cells and made millions selling them to drug companies."

Systemic inequality. Henrietta Lacks' story is inextricably linked to the racial and economic disparities of her time. As poor, African American tobacco farmers in the segregated South, the Lacks family had limited access to education and healthcare.

Medical exploitation:

• Henrietta was treated in the "colored" ward of Johns Hopkins Hospital

• Her cells were taken without her knowledge or consent

• The family was not informed about the cells for decades

• Researchers later took blood samples from family members without fully explaining why

This case highlighted the long history of medical exploitation of marginalized communities, from the Tuskegee syphilis experiments to the use of African American bodies for medical training and research without consent.

"Deborah's voice was utterly calm, her usual nervous laugh gone. 'I hope He's got our back on this one.'"

A shocking discovery. The Lacks family only learned about HeLa cells in the 1970s, two decades after Henrietta's death. This revelation sparked a range of emotions and reactions within the family, from anger and confusion to pride and a desire for recognition.

The family's evolving response:

• Initial shock and feelings of exploitation

• Attempts to understand the science behind HeLa cells

• Deborah's quest for information about her mother and sister

• Struggles with the media attention and scientists seeking their DNA

• Gradual acceptance and pride in Henrietta's contribution to science

• Advocacy for recognition and ethical considerations in tissue research

The Lacks family's journey reflects the complex emotions and challenges faced by those unexpectedly thrust into the spotlight of scientific history.

"Deborah's face fell. She'd heard many times that she'd inherited some of the DNA inside those cells from her mother. She didn't want to hear that her mother's cancer was in that DNA too."

A personal mission. Deborah Lacks, Henrietta's youngest daughter, became the family's most passionate advocate for understanding and recognition. Her quest to learn about her mother and the HeLa cells became a central thread in the story.

Deborah's journey:

• Overcoming fear and suspicion of scientists and journalists

• Learning about cell biology and medical research

• Seeking information about her mother's life and death

• Uncovering the tragic story of her sister Elsie, who died in a mental institution

• Struggling with the emotional weight of her family's legacy

• Finding a balance between pride in her mother's contribution and anger at past injustices

Deborah's story humanizes the scientific narrative, showing the personal impact of medical research on patients' families.

"Moore wasn't awarded any of the profits, but the judge did agree with him on two counts: lack of informed consent, because Golde hadn't disclosed his financial interests, and breach of fiduciary duty, meaning Golde had taken advantage of his position as doctor and violated patient trust."

A legal precedent. The case of John Moore, who sued his doctor for profiting from his cells without his knowledge, brought the issue of tissue ownership and commercialization to the forefront of legal and ethical debates.

Key aspects of the Moore case:

• Moore's doctor patented a cell line derived from Moore's spleen

• The cell line was valued at $3 billion

• Moore sued for a share of the profits

• The California Supreme Court ruled that Moore had no right to his discarded cells

• The case highlighted the need for informed consent and disclosure of potential commercial interests

This landmark case set the stage for ongoing debates about patient rights, tissue ownership, and the commercialization of human biological materials.

"There are, essentially, two issues to deal with: consent and money. For most people, knowing if and how their tissues are being used in research is a far bigger issue than profiting from them."

Complex ethical landscape. The HeLa story and subsequent cases have sparked ongoing debates about the ethics of tissue research and the rights of donors.

Key ethical issues:

• Informed consent for tissue collection and use

• Ownership of tissues once removed from the body

• Right to control how tissues are used in research

• Profit-sharing from commercially successful cell lines

• Privacy concerns related to genetic information

• Balancing scientific progress with individual rights

These debates have led to changes in research practices and regulations, but many questions remain unresolved as science continues to advance.

"If you could pile all HeLa cells ever grown onto a scale, they'd weigh more than 50 million metric tons—an inconceivable number, given that an individual cell weighs almost nothing."

A scientific powerhouse. HeLa cells have been instrumental in countless scientific breakthroughs and continue to be a vital tool in medical research.

Key contributions of HeLa cells:

• Development of the polio vaccine

• Advances in cancer and AIDS research

• Improved understanding of cell biology

• Testing effects of radiation and toxic substances

• Space research on cell behavior in zero gravity

• Gene mapping and cloning techniques

• In vitro fertilization advancements

The ubiquity and versatility of HeLa cells have made them an indispensable part of modern biomedical research, contributing to numerous Nobel Prize-winning discoveries.

"Deborah and Zakariyya stared at the screen like they'd gone into a trance, mouths open, cheeks sagging. It was the closest they'd come to seeing their mother alive since they were babies."

Personal sacrifice. While HeLa cells have advanced science immeasurably, the story of Henrietta Lacks and her family reminds us of the human cost behind scientific progress.

The Lacks family's struggles:

• Lack of access to healthcare despite their mother's cells' contribution to medicine

• Emotional distress from learning about HeLa cells decades after Henrietta's death

• Privacy violations as their genetic information became public

• Financial hardship while others profited from HeLa cells

• Confusion and fear about the nature of the cells and their mother's "immortality"

The Lacks story highlights the importance of considering the human impact of scientific research and the need for ethical practices that respect the dignity of research subjects and their families.

"How you should feel about all this isn't obvious. It's not as if scientists are stealing your arm or some vital organ. They're using tissue scraps you parted with voluntarily. Still, that often involves someone taking part of you."

A complex balance. The HeLa story has contributed to ongoing efforts to reconcile the needs of scientific progress with ethical considerations and human rights.

Key developments and proposals:

• Improved informed consent procedures

• Debates about tissue ownership and control

• Calls for benefit-sharing from profitable discoveries

• Enhanced privacy protections for genetic information

• Efforts to increase diversity and representation in tissue research

• Proposals for compensating tissue donors

• Ongoing discussions about the ethics of gene patenting

As science continues to advance, society must grapple with these issues to ensure that progress is made ethically and with respect for human dignity.