Three-Parent Embryos:
Gearing up for the U.S. Debate
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INTRODUCTION
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On February 24th, 2015 the House of Lords
approved a law permitting the IVF
production of three-parent embryos to
prevent the maternal transmission of
mitochondrial disease. In October, the UK’s
Human Fertilization and Embryo Authority
will license British clinics to use
mitochondrial replacement for human
trials. The arrival of Britain’s first three-
parent baby is expected by 2016.
Meanwhile, across the pond, the U.S. Food and Drug
Administration has already assessed risks and benefits of
mitochondrial replacement (MR), made recommendations
regarding its use in human clinical trials as a treatment for age-
related infertility, and commissioned the Institute of Medicine to
present a final consensus report on all associated ethical and
social policy issues. The Consensus Study Committee held its first
meeting in January, 2015. It will convene again in March and
May with the inclusion of public comment sessions, and will
draft and finalize the consensus report during its last two closed
door meetings. If MR is approved by the FDA, American clinicians
could submit an application and, if deemed eligible, could
inaugurate the production of three-parent embryos in human
clinical trials in the not-so-distant future.
Here, I argue two things. First, the
enormous moral and social harm of MR
and its production of three-parent embryos
outweighs the good of preventing a subset
of mito-diseases. Second, anyone interested
in protecting human life, human dignity,
human procreation, and the human
genome should subscribe to the following
three-step plan so that the voice of reason
can be heard during the upcoming U.S.
debate
on three-parent embryos.
I
STEP ONE:
Understand the science of MR
P
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Maternal Spindle Transfer
I
STEP TWO:
Recognize the Moral Case Against MR
STEP TWO:
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The PNT technique of MR
involves the intentional
destruction of the life of a
human embryo.
Both MR techniques distort the
meaning of parenthood and
human procreation, deny the
IVF child its basic right to life
and to be loved unconditionally,
and contradict the child’s
fundamental equality with his
parents.
MR endangers
the human
genome.
MR abuses the
women who donate
their eggs.
I
STEP THREE:
Identify and deflect
misrepresentations of MR advocates.
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MR will eliminate
mito-diseases in
future children.
MR will be in great
demand because one in
200 babies is born with
mitochondrial diseases.
MR will save
lives.
MR has been
adequately studied
in animals and,
therefore, is safe.
A majority of
the public
supports MR.
Except through MR
techniques, the woman
with mutated mtDNA has
no other option for family
building.
MR will not lead to more
controversial practices;
the slippery slope
argument is exaggerated.
The genetic
contribution of the
mito-donor is
inconsequential.
Mito-donation is no more
dangerous or
controversial than organ
donation.
I
STEP FOUR:
Let the voice of reason be
heard!
P
M
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Armed with: (1) an adequate
knowledge of the science of MR, (2) the
ability to identify and correct
misrepresentations from MR advocacy
groups, and (3) a comprehensive grasp
of the moral case against MR, compose
a succinct, cogent statement explaining
your opposition to MR and its
production of three-parent embryos
and present it to the Institute of
Medicine.
The IOM Consensus Committee will hold meetings
open for public comment on March 31st (8:30 AM
– 5 PM) through April 1st (8:30 AM until noon)
and on May – (8:30 AM – 5 PM) through May –
(8:30 AM until noon). If you live in the DC area
and wish to present your position statement orally,
simply show up at the Institute of Medicine on
those dates (500 Fifth St. NW). If at a distance,
submit your comments either by email
(MitoEthics@nas.edu) or by US mail (Attn:
Michael Berrios; Institute of Medicine; 500 Fifth
St. NW, Washington, DC 20001).
Three-Parent Embryos:
Gearing up for the U.S. Debate
P
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Mitoethics

  • 1.
    Three-Parent Embryos: Gearing upfor the U.S. Debate P M D
  • 2.
  • 3.
    On February 24th,2015 the House of Lords approved a law permitting the IVF production of three-parent embryos to prevent the maternal transmission of mitochondrial disease. In October, the UK’s Human Fertilization and Embryo Authority will license British clinics to use mitochondrial replacement for human trials. The arrival of Britain’s first three- parent baby is expected by 2016.
  • 4.
    Meanwhile, across thepond, the U.S. Food and Drug Administration has already assessed risks and benefits of mitochondrial replacement (MR), made recommendations regarding its use in human clinical trials as a treatment for age- related infertility, and commissioned the Institute of Medicine to present a final consensus report on all associated ethical and social policy issues. The Consensus Study Committee held its first meeting in January, 2015. It will convene again in March and May with the inclusion of public comment sessions, and will draft and finalize the consensus report during its last two closed door meetings. If MR is approved by the FDA, American clinicians could submit an application and, if deemed eligible, could inaugurate the production of three-parent embryos in human clinical trials in the not-so-distant future.
  • 5.
    Here, I arguetwo things. First, the enormous moral and social harm of MR and its production of three-parent embryos outweighs the good of preventing a subset of mito-diseases. Second, anyone interested in protecting human life, human dignity, human procreation, and the human genome should subscribe to the following three-step plan so that the voice of reason can be heard during the upcoming U.S. debate on three-parent embryos.
  • 6.
    I STEP ONE: Understand thescience of MR P M D
  • 11.
  • 12.
    I STEP TWO: Recognize theMoral Case Against MR STEP TWO: P M D
  • 13.
    The PNT techniqueof MR involves the intentional destruction of the life of a human embryo.
  • 14.
    Both MR techniquesdistort the meaning of parenthood and human procreation, deny the IVF child its basic right to life and to be loved unconditionally, and contradict the child’s fundamental equality with his parents.
  • 15.
  • 16.
    MR abuses the womenwho donate their eggs.
  • 17.
    I STEP THREE: Identify anddeflect misrepresentations of MR advocates. P D M
  • 18.
  • 19.
    MR will bein great demand because one in 200 babies is born with mitochondrial diseases.
  • 20.
  • 21.
    MR has been adequatelystudied in animals and, therefore, is safe.
  • 22.
    A majority of thepublic supports MR.
  • 23.
    Except through MR techniques,the woman with mutated mtDNA has no other option for family building.
  • 24.
    MR will notlead to more controversial practices; the slippery slope argument is exaggerated.
  • 25.
    The genetic contribution ofthe mito-donor is inconsequential.
  • 26.
    Mito-donation is nomore dangerous or controversial than organ donation.
  • 27.
    I STEP FOUR: Let thevoice of reason be heard! P M D
  • 28.
    Armed with: (1)an adequate knowledge of the science of MR, (2) the ability to identify and correct misrepresentations from MR advocacy groups, and (3) a comprehensive grasp of the moral case against MR, compose a succinct, cogent statement explaining your opposition to MR and its production of three-parent embryos and present it to the Institute of Medicine.
  • 29.
    The IOM ConsensusCommittee will hold meetings open for public comment on March 31st (8:30 AM – 5 PM) through April 1st (8:30 AM until noon) and on May – (8:30 AM – 5 PM) through May – (8:30 AM until noon). If you live in the DC area and wish to present your position statement orally, simply show up at the Institute of Medicine on those dates (500 Fifth St. NW). If at a distance, submit your comments either by email (MitoEthics@nas.edu) or by US mail (Attn: Michael Berrios; Institute of Medicine; 500 Fifth St. NW, Washington, DC 20001).
  • 30.
    Three-Parent Embryos: Gearing upfor the U.S. Debate P M D