Exploring the controversial claims of CRISPR-edited babies and the ethical implications of modifying human embryos
In November 2018, the world of science experienced a seismic shock that would forever change the conversation about genetic engineering. Chinese scientist He Jiankui announced he had secretly created the world's first gene-edited babies - twin girls born from embryos modified using CRISPR technology. The international scientific community reacted with universal condemnation, describing the work as "monstrous," "unethical," and "a huge blow to the reputation of Chinese science." He was subsequently imprisoned for three years for violating medical regulations 3 .
Visual representation of gene editing technology
Yet, just seven years later, we're witnessing a surprising reboot of this controversial frontier. Silicon Valley venture capitalists, futurists, and entrepreneurs are now pushing to advance the very technology that once horrified the global scientific establishment 3 . This article explores the shocking claims, the science behind them, and why the quest to create genetically modified babies has returned with renewed force - raising profound questions about how we define humanity itself.
Targets non-reproductive cells and affects only the individual receiving treatment. The genetic changes are not inherited by future generations. This approach has produced breakthrough therapies for conditions like sickle cell disease and is widely considered ethical 1 .
CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a revolutionary gene-editing system derived from a natural defense mechanism in bacteria. The system consists of two key components:
Acts as "molecular scissors" that cut DNA at precise locations 9
A short RNA sequence that directs Cas9 to the specific target gene 9
When the cell repairs the cut DNA, researchers can disrupt, delete, or insert new genetic sequences. More recent advancements like base editing and prime editing allow even more precise changes without breaking both strands of DNA 9 .
In 2018, He Jiankui and his team performed what many consider a reckless human experiment. Their goal was to create children resistant to HIV by targeting the CCR5 gene, which encodes a protein HIV uses to enter cells 3 .
Researchers created multiple embryos through in vitro fertilization using sperm from HIV-positive fathers and eggs from healthy mothers.
At the single-cell stage, they injected CRISPR-Cas9 components designed to disable the CCR5 gene.
They screened the edited embryos to verify the genetic modifications.
Selected embryos were implanted, resulting in the birth of twin girls nicknamed "Lulu" and "Nana."
The team conducted genetic testing during pregnancy and after birth to assess the editing outcomes.
The experiment was flawed on multiple levels, both scientifically and ethically:
The genetic changes didn't appear uniformly across all cells, creating "mosaic" embryos with mixed genetics 3
Participants weren't fully informed about the experimental nature and potential risks
Other effective methods exist to prevent HIV transmission from father to child
The experiment targeted a gene associated with normal immune function, potentially creating unintended health consequences while offering debatable benefits 3 .
Aspect | He Jiankui's Experiment | Ethical Gene Therapy |
---|---|---|
Target Cells | Embryos (germline) | Somatic cells only |
Inheritance | Changes passed to future generations | Changes affect only the individual |
Medical Justification | Questionable (alternative prevention exists) | Treats serious diseases with no alternatives |
Regulatory Oversight | Bypassed ethical review | Rigorous oversight and approval |
Informed Consent | Inadequate and misleading | Comprehensive and transparent |
Understanding CRISPR technology requires familiarity with the essential laboratory components that make precise genetic editing possible:
Research Reagent | Function | Application in Experiments |
---|---|---|
Cas9 Protein | DNA-cutting enzyme ("molecular scissors") | Creates double-strand breaks in target DNA sequences |
Guide RNA (gRNA) | RNA molecule that targets specific DNA sequences | Directs Cas9 to precise genomic locations for editing |
Protospacer Adjacent Motif (PAM) | Short DNA sequence adjacent to target site | Essential for Cas9 recognition and binding |
Lipid Nanoparticles (LNPs) | Delivery vehicle for CRISPR components | Safely transports editing tools to target cells in vivo |
Base Editors | Modified CRISPR systems that change single DNA letters | Enables more precise editing without DNA breaks |
Homology-Directed Repair (HDR) Template | DNA template containing desired sequence | Guides precise cellular repair to insert specific genes |
Laboratory equipment used in genetic research
Visualization of DNA structure
Despite the ongoing ethical debate, private companies are now openly pursuing germline editing:
In 2025, entrepreneur Cathy Tie launched a company called "Manhattan Project" with the explicit goal of developing germline editing to prevent genetic diseases. Tie states: "We want to be the company that does this in the light, with transparency and with good intentions" 3 .
The company plans to:
Other groups with different motivations are also entering the space:
This emerging landscape has created unlikely alliances between medical researchers, venture capitalists, and futurists - all pushing boundaries in different directions.
Group | Stated Goals | Ethical Stance | Approach |
---|---|---|---|
Academic Researchers | Basic research, understand human development | Cautious, favor moratorium | Incremental, transparent |
Medical Companies | Eliminate genetic diseases | Therapeutic focus only | Regulatory compliance |
Pronatalists | Increase births, improve child health | Supportive of technology | Rapid advancement |
Transhumanists | Enhance human capabilities beyond health | Strongly supportive | Boundary-pushing |
Based on survey data of public attitudes toward germline editing applications
In response to these developments, major scientific organizations have pushed back:
Three leading gene therapy trade organizations called for a 10-year international moratorium on germline editing 8
The Alliance for Regenerative Medicine stated: "Human heritable gene editing is clearly a terrible solution in search of a problem" 8
Critics argue mistakes would be permanent and heritable, affecting all future generations 8
The regulatory environment varies significantly by country, with some nations having strict bans while others offer more permissive environments for research.
"Move fast and break things has not worked very well for Silicon Valley in health care. When you talk about reproduction, the things you are breaking are babies."
The shock that greeted the first CRISPR baby claims has evolved into a complex global conversation about the future of human evolution. As Stanford bioethicist Hank Greely warns: "Move fast and break things has not worked very well for Silicon Valley in health care. When you talk about reproduction, the things you are breaking are babies" 3 .
The scientific community faces a critical challenge: how to harness the legitimate potential of gene editing to prevent suffering from genetic diseases while establishing strong safeguards against unethical applications. As companies like Manhattan Project begin their work, and as He Jiankui himself has reemerged advocating for gene editing to help humanity "fight back" against threats like AI, the need for informed public engagement has never been greater 3 .
The ethical dilemma of genetic engineering
The question is no longer whether we can edit human embryos, but whether we should - and who gets to decide where we draw these fundamental boundaries of life itself. The answer will shape the future of our species for generations to come.