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#9 The Immortal Life Of Henrietta Lacks


Henrietta Lacks, a remarkable but lesser-known figure, played a pivotal role in countless scientific advancements. Despite succumbing to cervical cancer in 1951, her malignant cells, taken without her knowledge, became immortalized and were shared for research with academic and industrial institutions across the World.

Her cells, known as 'HeLa cells,' hold the key to their immortality in an active enzyme called telomerase that replenishes protective structures, known as telomeres, during cell division. This allows them to bypass the normal limit of cell divisions (the Hayflick limit) and divide indefinitely. 

This characteristic of cellular immortality makes HeLa cells ideal for any research requiring a constant supply of rapidly growing human cells. They have fueled numerous medical breakthroughs like the development of polio vaccine, in-vitro fertilization, understanding cancer cell behavior, standardizing cell culturing, and testing the safety and efficacy of new drugs and vaccines (including the recent COVID-19 vaccine). 

Tragically, despite the immense contribution of HeLa cells, their industrial-scale culturing and commercialization, Henrietta's family remained unaware (until late 1960s) and received no compensation (until 2023). Through her book, "The Immortal Life of Henrietta Lacks," author Rebecca Skloot sheds light on this ethical lapse and the dark side of medical history, where informed consent was often disregarded, particularly for marginalized communities like Henrietta's. 

By interweaving Henrietta's story with that of her daughter, Deborah Lacks, who fought for her mother's recognition and sought answers about her cells, the author delves into issues such as racism, informed consent, patient confidentiality, and fiduciary duty. Importantly, she also considers potential counterarguments concerning strict informed consent protocols and their potential to hinder scientific advancement, encouraging a balanced discussion.

Ultimately, Skloot's poignant tale, centered around the Lacks family, serves as a powerful call for ethical reform in biomedicine. Her narrative advocates for the development of scientific temper, humanism, and a spirit of inquiry that prioritizes both scientific progress and ethical considerations. Henrietta Lacks' story reminds us to acknowledge the human cost of scientific advancements and strive for a future where research is conducted with transparency, respect, and justice for all!


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