Request for Public Comment on the Proposed Changes to the NIH Guidelines for Human Stem Cell Research and the Proposed Scope of an NIH Steering Committee's Consideration of Certain Human-Animal Chimera Research, 51921-51923 [2016-18601]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
mstockstill on DSK3G9T082PROD with NOTICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: AIDS and AIDS Related Research.
Date: August 9, 2016.
Time: 11:00 a.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Mark P. Rubert, Ph.D.,
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Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5218,
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1775, rubertm@csr.nih.gov.
This notice is being published less than 15
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Name of Committee: Center for Scientific
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Date: August 9, 2016.
Time: 11:00 a.m. to 1:00 p.m.
Agenda: To review and evaluate grant
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Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Shalanda A. Bynum,
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for Scientific Review, National Institutes of
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This notice is being published less than 15
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Name of Committee: Center for Scientific
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Conflict: AIDS and Related Research
Applications.
Date: August 9, 2016.
Time: 1:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
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Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Robert Freund, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5216,
MSC 7852, Bethesda, MD 20892, 301–435–
1050, freundr@csr.nih.gov.
This notice is being published less than 15
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limitations imposed by the review and
funding cycle.
Name of Committee: Center for Scientific
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SPF Macaque Colonies.
Date: August 12, 2016.
Time: 12:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Shiv A. Prasad, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5220,
MSC 7852, Bethesda, MD 20892, 301–443–
5779, prasads@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: August 1, 2016.
Anna Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–18548 Filed 8–4–16; 8:45 am]
BILLING CODE 4140–01–P
Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel NIAID Clinical Trial
Implementation Grant (R01).
Date: September 1, 2016
Time: 1:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health RM
5C100, 5601 Fishers Lane, Rockville, MD
20892 (Telephone Conference Call).
Contact Person: Lynn Rust, Ph.D.,
Scientific Review Officer, Scientific Review
Program, Division of Extramural Activities,
Room 3G42A National Institutes of Health/
NIAID, 5601 Fishers Lane, MSC 9823,
Bethesda, MD 20892–9823, (240) 669–5069,
lrust@niaid.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.855, Allergy, Immunology,
and Transplantation Research; 93.856,
Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
Dated: August 1, 2016.
Anna Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–18550 Filed 8–4–16; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Request for Public Comment on the
Proposed Changes to the NIH
Guidelines for Human Stem Cell
Research and the Proposed Scope of
an NIH Steering Committee’s
Consideration of Certain HumanAnimal Chimera Research
The National Institutes of
Health (NIH) is requesting public
comment on a proposal to amend
Section IV and Section V of the NIH
Guidelines for Human Stem Cell
Research and on the proposed scope of
certain human-animal chimera research
that will be considered internally by an
NIH steering committee to provide
programmatic input to the director of
the relevant NIH Institute(s) or Center(s)
or equivalent NIH officials responsible
for funding decisions.
DATES: Written comments must be
received by the NIH on or before
September 6, 2016 in order to be
considered.
ADDRESSES: Public comments may be
entered at: https://grants.nih.gov/grants/
rfi/rfi.cfm?ID=57. Comments may also
be mailed to: Office of Science Policy,
National Institutes of Health, 6705
Rockledge Drive, Suite 750, Bethesda,
MD 20892, 301–496–9838. Comments
will be made publicly available.
Comments received, including any
SUMMARY:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
PO 00000
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E:\FR\FM\05AUN1.SGM
05AUN1
mstockstill on DSK3G9T082PROD with NOTICES
51922
Federal Register / Vol. 81, No. 151 / Friday, August 5, 2016 / Notices
personal information, will be posted
without change to https://grants.nih.gov/
grants/rfi/responses_57.cfm.
SUPPLEMENTARY INFORMATION: On July 7,
2009, the NIH issued the NIH
Guidelines for Human Stem Cell
Research (‘‘Guidelines’’) 74 FR 32170
(July 7, 2009) to implement Executive
Order 13505 (March 9, 2009), as it
pertains to NIH-funded stem cell
research, to establish policy and
procedures under which the NIH will
fund such research, and help ensure
that NIH-funded research in this area is
ethically responsible, scientifically
worthy, and conducted in accordance
with applicable law.
Since the Guidelines were issued in
2009, growing knowledge and
advancement of stem cell biology has
created new research opportunities.
Some scientists are exploring strategies
for growing human tissue and organs in
animals through the introduction of
human pluripotent cells into early stage
embryos of non-human vertebrate
animals. These experimental designs
raise questions regarding where the
human cells might go in the developing
animal and how they might function,
such as whether the human cells might
contribute to the central nervous system
and affect the cognition of the animal.
While considering these issues, on
September 23, 2015, the NIH issued a
funding moratorium (https://
grants.nih.gov/grants/guide/notice-files/
NOT-OD-15-158.html) on ‘‘NIH
Research Involving Introduction of
Human Pluripotent Cells into NonHuman Vertebrate Animal PreGastrulation Embryos.’’ The NIH
subsequently held a workshop with
experts on November 6, 2015, to review
the state of the science and discuss
animal welfare issues.
The workshop illustrated that while
there are significant challenges to
creating chimeric models, there is clear
interest and potential in producing
animal models with human tissues or
organs for studying human
development, disease pathology, and
eventually organ transplantation. In the
interest of moving the field forward
while preserving the NIH’s opportunity
to provide continuing assessment and
oversight of this emerging area of
research, the NIH has decided to
establish a steering committee to
provide programmatic input to the
director of the relevant NIH Institute(s)
or Center(s) (or equivalent NIH official
responsible for funding decisions) on
certain human-animal chimera research
proposals. The committee will be
composed of federal employees. The
committee is expected to consider and
VerDate Sep<11>2014
17:42 Aug 04, 2016
Jkt 238001
offer the director of the relevant NIH
Institute(s) or Center(s) (or equivalent
NIH official responsible for funding
decisions) programmatic input on
factors, such as, (1) the characteristics of
the human cells to be introduced
(including potency and any
modifications of those cells); (2)
characteristics of the recipient animal
(e.g., species, stage of development, and
any modifications that affect location or
function of human cells); (3) other data
relevant to the likely effects on the
animal (e.g., changes in cognition,
behavior, or physical appearance); (4)
planned monitoring (including animal
welfare assessments); and (5) any
staging of proposed research (e.g.,
assessing the outcome of a particular
experiment before conducting a further
experiment). This internal
programmatic work will be conducted
independent of, and in addition to, the
usual peer review procedures for
research at the NIH. The relevant IC
director(s) will consider the input from
the steering committee, in addition to
other NIH programmatic input, as well
as the funding recommendations and
evaluations of the initial Scientific
Review Group and the relevant Institute
or Center’s Advisory Council or Board.
The committee will also monitor trends
in this general field of research and the
use of new technologies, and may
provide such analysis and advice to the
NIH leadership.
The NIH also proposes to revise the
Guidelines to expand the existing
prohibition on introducing human
pluripotent stem cells into blastocyst
stage nonhuman primate embryos to
include pre-blastocyst stage nonhuman
primate embryos; and to expand the
prohibition on research involving the
breeding of animals where the
introduction of hESCs or human
induced pluripotent stem cells may
contribute to the germ line to include
any human cells that may result in the
formation of human gametes.
Therefore, NIH is requesting public
comment on:
(1) The following proposed changes to
the Guidelines.
Sections IV and V of the Guidelines
currently state:
IV. Research Using hESCs and/or Human
Induced Pluripotent Stem Cells That,
Although the Cells May Come From Eligible
Sources, Is Nevertheless Ineligible for NIH
Funding
This section governs research using hESCs
and human induced pluripotent stem cells,
i.e., human cells that are capable of dividing
without differentiating for a prolonged period
in culture, and are known to develop into
cells and tissues of the three primary germ
layers. Although the cells may come from
PO 00000
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Fmt 4703
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eligible sources, the following uses of these
cells are nevertheless ineligible for NIH
funding, as follows:
A. Research in which hESCs (even if
derived from embryos donated in accordance
with these Guidelines) or human induced
pluripotent stem cells are introduced into
non-human primate blastocysts.
B. Research involving the breeding of
animals where the introduction of hESCs
(even if derived from embryos donated in
accordance with these Guidelines) or human
induced pluripotent stem cells may
contribute to the germ line.
V. Other Research Not Eligible for NIH
Funding
A. NIH funding of the derivation of stem
cells from human embryos is prohibited by
the annual appropriations ban on funding of
human embryo research (Section 509,
Omnibus Appropriations Act, 2009, Pub. L.
111–8, 3/11/09), otherwise known as the
Dickey Amendment.
B. Research using hESCs derived from
other sources, including somatic cell nuclear
transfer, parthenogenesis, and/or IVF
embryos created for research purposes, is not
eligible for NIH funding.
The NIH is proposing to amend the
Guidelines as follows:
IV. Research Not Eligible for NIH Funding:
A. Research in which human pluripotent
stem cells are introduced into non-human
primate embryos up through the end of the
blastocyst stage, is not eligible for funding.
B. Research involving the breeding of
animals where the introduction of human
cells may contribute to the germ line, is not
eligible for funding.
C. NIH funding of the derivation of stem
cells from human embryos is prohibited by
the annual appropriations limitations on the
funding of human embryo research (see e.g.
Section 508, Omnibus Appropriations Act,
2016, Pub. L.114–113, 12/18/15), otherwise
known as the Dickey Amendment.
D. Research using hESCs derived from
other sources, including somatic cell nuclear
transfer, parthenogenesis, and/or IVF
embryos created for research purposes, is not
eligible for NIH funding.
(2) The NIH is also requesting public
comment on the proposed scope of
research (e.g., grant applications,
contract proposals, intramural research
protocols, etc.) to be considered by an
NIH steering committee to provide
programmatic input to the director of
the relevant Institute or Center (or
equivalent NIH official responsible for
funding decisions). The NIH proposes
the scope of research include research
in which:
a. Human pluripotent cells are
introduced into non-human vertebrate
embryos, up through the end of the
gastrulation stage, or
b. human cells are introduced into
post-gastrulation non-human mammals
(excluding rodents), such that there
could be either a substantial
contribution or a substantial functional
E:\FR\FM\05AUN1.SGM
05AUN1
Federal Register / Vol. 81, No. 151 / Friday, August 5, 2016 / Notices
modification to the animal brain by the
human cells.
While the NIH seeks public comment
on the proposed changes to the
Guidelines, and on the proposed scope
for an NIH steering committee’s
consideration of certain research, NOT–
OD–15–158 will remain in effect.
Dated: July 28, 2016.
Lawrence A. Tabak,
Deputy Director, National Institutes of Health.
[FR Doc. 2016–18601 Filed 8–4–16; 8:45 am]
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
[Docket No. USCG–2016–0640]
Eighth Coast Guard District; Interim
Outer Continental Shelf Risk-Based
Resource Allocation Methodology
Coast Guard, DHS.
Notice of availability and
request for comments.
AGENCY:
ACTION:
BILLING CODE 4140–01–P
The Coast Guard announces
the availability of an interim risk based
resource allocation methodology for
inspections of certain Outer Continental
Shelf (OCS) units in the Eighth Coast
Guard District (D8) area of responsibility
(AOR). This interim methodology will
be implemented for a five-month trial
period beginning August 1, 2016. After
the trial period, the methodology will be
finalized within D8 and submitted to
Coast Guard Headquarters (CG–CVC) for
consideration at the national level.
DATES: Comments and related material
must be received by the Coast Guard on
or before September 6, 2016.
ADDRESSES: You may submit comments
identified by docket number USCG–
2016–0640 or view documents
mentioned in this notice as being
available in the docket using the Federal
eRulemaking Portal at https://
www.regulations.gov. See the ‘‘Public
Participation and Request for
Comments’’ portion of the
SUPPLEMENTARY INFORMATION section for
further instructions on submitting
comments.
SUMMARY:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood
Institute; Notice of Closed Meeting
mstockstill on DSK3G9T082PROD with NOTICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Heart, Lung,
and Blood Institute, Special Emphasis Panel,
Pediatric Heart Network Data Coordinating
Centers (U24).
Date: August 30, 2016.
Time: 2:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Room 7182, Bethesda, MD
20892, (Telephone Conference Call).
Contact Person: Susan Wohler Sunnarborg,
Ph.D., Scientific Review Officer, Office of
Scientific Review/DERA National, Heart,
Lung, and Blood Institute, 6701 Rockledge
Drive, Room 7182, Bethesda, MD 20892
sunnarborgsw@nhlbi.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
Dated: July 29, 2016.
Carolyn Baum,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–18549 Filed 8–4–16; 8:45 am]
BILLING CODE 4140–01–P
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17:42 Aug 04, 2016
Jkt 238001
For
information about this document call or
email Steve Sutton, Coast Guard;
telephone 202-671–2151, email
steve.sutton@uscg.mil.
SUPPLEMENTARY INFORMATION:
FOR FURTHER INFORMATION CONTACT:
Discussion
This interim risk based resource
allocation methodology is intended to
improve implementation of the
requirements contained in 33 CFR
140.101(c), 143.120(c), and 143.210(a)
by employing interagency consultation
and by establishing increased focus on
the industrial mission and regulatory
compliance and casualty data. It builds
upon the risk based matrix created for
foreign Mobile Offshore Drilling Units
(MODU), which was published in the
Federal Register (76 FR 39885) by the
Coast Guard in 2011 by applying similar
principles to other OCS units and
adding consultation with the Bureau of
Safety and Environmental Enforcement
(BSEE). This methodology will
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51923
reallocate Coast Guard inspection
resources from lower risk, fixed interval
activities to higher risk activities prior
to commencing an industrial mission.
The Coast Guard will periodically
evaluate MODUs and OCS facilities that
either perform drilling or well-workover
or are due for a Coast Guard regulatory
inspection to assign an inspection
priority and scope using risk matrices.
For example, under this methodology
Coast Guard inspection resources
previously used to conduct an annual
Certificate of Compliance inspection of
a lower risk stacked MODU may be
reallocated to conduct a higher risk
inspection of any MODU or OCS facility
with a drilling rig prior to
commencement of drilling.
Outreach to the Offshore Operator’s
Committee
On June 8, 2016, the Coast Guard
conducted outreach to the offshore
Operators’ Committee at its annual
general meeting in Houston, TX. The
presentation, presentation script, and
transcript of questions and answers
from this outreach are available on the
docket where indicated under
ADDRESSES.
Public Participation and Request for
Comments
We encourage you to submit
comments (or related material) on the
interim risk based resource allocation
methodology for inspection of OCS
units in the D8 AOR. We will consider
all submissions and may adjust our
action based on your comments,
although we do not anticipate a written
response to comments. If you submit a
comment, please include the docket
number for this notice, indicate the
specific section of this document to
which each comment applies, and
provide a reason for each suggestion or
recommendation.
We encourage you to submit
comments through the Federal
eRulemaking Portal at https://
www.regulations.gov. If your material
cannot be submitted using https://
www.regulations.gov, contact the person
in the FOR FURTHER INFORMATION
CONTACT section of this document for
alternate instructions. Documents
mentioned in this notice of availability,
and all public comments, are in our
online docket at https://
www.regulations.gov and can be viewed
by following that Web site’s
instructions. Additionally, if you go to
the online docket and sign up for email
alerts, you will be notified when
comments are posted to the docket.
We accept anonymous comments. All
comments received will be posted
E:\FR\FM\05AUN1.SGM
05AUN1
Agencies
[Federal Register Volume 81, Number 151 (Friday, August 5, 2016)]
[Notices]
[Pages 51921-51923]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-18601]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Request for Public Comment on the Proposed Changes to the NIH
Guidelines for Human Stem Cell Research and the Proposed Scope of an
NIH Steering Committee's Consideration of Certain Human-Animal Chimera
Research
SUMMARY: The National Institutes of Health (NIH) is requesting public
comment on a proposal to amend Section IV and Section V of the NIH
Guidelines for Human Stem Cell Research and on the proposed scope of
certain human-animal chimera research that will be considered
internally by an NIH steering committee to provide programmatic input
to the director of the relevant NIH Institute(s) or Center(s) or
equivalent NIH officials responsible for funding decisions.
DATES: Written comments must be received by the NIH on or before
September 6, 2016 in order to be considered.
ADDRESSES: Public comments may be entered at: https://grants.nih.gov/grants/rfi/rfi.cfm?ID=57. Comments may also be mailed to: Office of
Science Policy, National Institutes of Health, 6705 Rockledge Drive,
Suite 750, Bethesda, MD 20892, 301-496-9838. Comments will be made
publicly available. Comments received, including any
[[Page 51922]]
personal information, will be posted without change to https://grants.nih.gov/grants/rfi/responses_57.cfm.
SUPPLEMENTARY INFORMATION: On July 7, 2009, the NIH issued the NIH
Guidelines for Human Stem Cell Research (``Guidelines'') 74 FR 32170
(July 7, 2009) to implement Executive Order 13505 (March 9, 2009), as
it pertains to NIH-funded stem cell research, to establish policy and
procedures under which the NIH will fund such research, and help ensure
that NIH-funded research in this area is ethically responsible,
scientifically worthy, and conducted in accordance with applicable law.
Since the Guidelines were issued in 2009, growing knowledge and
advancement of stem cell biology has created new research
opportunities. Some scientists are exploring strategies for growing
human tissue and organs in animals through the introduction of human
pluripotent cells into early stage embryos of non-human vertebrate
animals. These experimental designs raise questions regarding where the
human cells might go in the developing animal and how they might
function, such as whether the human cells might contribute to the
central nervous system and affect the cognition of the animal.
While considering these issues, on September 23, 2015, the NIH
issued a funding moratorium (https://grants.nih.gov/grants/guide/notice-files/NOT-OD-15-158.html) on ``NIH Research Involving Introduction of
Human Pluripotent Cells into Non-Human Vertebrate Animal Pre-
Gastrulation Embryos.'' The NIH subsequently held a workshop with
experts on November 6, 2015, to review the state of the science and
discuss animal welfare issues.
The workshop illustrated that while there are significant
challenges to creating chimeric models, there is clear interest and
potential in producing animal models with human tissues or organs for
studying human development, disease pathology, and eventually organ
transplantation. In the interest of moving the field forward while
preserving the NIH's opportunity to provide continuing assessment and
oversight of this emerging area of research, the NIH has decided to
establish a steering committee to provide programmatic input to the
director of the relevant NIH Institute(s) or Center(s) (or equivalent
NIH official responsible for funding decisions) on certain human-animal
chimera research proposals. The committee will be composed of federal
employees. The committee is expected to consider and offer the director
of the relevant NIH Institute(s) or Center(s) (or equivalent NIH
official responsible for funding decisions) programmatic input on
factors, such as, (1) the characteristics of the human cells to be
introduced (including potency and any modifications of those cells);
(2) characteristics of the recipient animal (e.g., species, stage of
development, and any modifications that affect location or function of
human cells); (3) other data relevant to the likely effects on the
animal (e.g., changes in cognition, behavior, or physical appearance);
(4) planned monitoring (including animal welfare assessments); and (5)
any staging of proposed research (e.g., assessing the outcome of a
particular experiment before conducting a further experiment). This
internal programmatic work will be conducted independent of, and in
addition to, the usual peer review procedures for research at the NIH.
The relevant IC director(s) will consider the input from the steering
committee, in addition to other NIH programmatic input, as well as the
funding recommendations and evaluations of the initial Scientific
Review Group and the relevant Institute or Center's Advisory Council or
Board. The committee will also monitor trends in this general field of
research and the use of new technologies, and may provide such analysis
and advice to the NIH leadership.
The NIH also proposes to revise the Guidelines to expand the
existing prohibition on introducing human pluripotent stem cells into
blastocyst stage nonhuman primate embryos to include pre-blastocyst
stage nonhuman primate embryos; and to expand the prohibition on
research involving the breeding of animals where the introduction of
hESCs or human induced pluripotent stem cells may contribute to the
germ line to include any human cells that may result in the formation
of human gametes.
Therefore, NIH is requesting public comment on:
(1) The following proposed changes to the Guidelines.
Sections IV and V of the Guidelines currently state:
IV. Research Using hESCs and/or Human Induced Pluripotent Stem
Cells That, Although the Cells May Come From Eligible Sources, Is
Nevertheless Ineligible for NIH Funding
This section governs research using hESCs and human induced
pluripotent stem cells, i.e., human cells that are capable of
dividing without differentiating for a prolonged period in culture,
and are known to develop into cells and tissues of the three primary
germ layers. Although the cells may come from eligible sources, the
following uses of these cells are nevertheless ineligible for NIH
funding, as follows:
A. Research in which hESCs (even if derived from embryos donated
in accordance with these Guidelines) or human induced pluripotent
stem cells are introduced into non-human primate blastocysts.
B. Research involving the breeding of animals where the
introduction of hESCs (even if derived from embryos donated in
accordance with these Guidelines) or human induced pluripotent stem
cells may contribute to the germ line.
V. Other Research Not Eligible for NIH Funding
A. NIH funding of the derivation of stem cells from human
embryos is prohibited by the annual appropriations ban on funding of
human embryo research (Section 509, Omnibus Appropriations Act,
2009, Pub. L. 111-8, 3/11/09), otherwise known as the Dickey
Amendment.
B. Research using hESCs derived from other sources, including
somatic cell nuclear transfer, parthenogenesis, and/or IVF embryos
created for research purposes, is not eligible for NIH funding.
The NIH is proposing to amend the Guidelines as follows:
IV. Research Not Eligible for NIH Funding:
A. Research in which human pluripotent stem cells are introduced
into non-human primate embryos up through the end of the blastocyst
stage, is not eligible for funding.
B. Research involving the breeding of animals where the
introduction of human cells may contribute to the germ line, is not
eligible for funding.
C. NIH funding of the derivation of stem cells from human
embryos is prohibited by the annual appropriations limitations on
the funding of human embryo research (see e.g. Section 508, Omnibus
Appropriations Act, 2016, Pub. L.114-113, 12/18/15), otherwise known
as the Dickey Amendment.
D. Research using hESCs derived from other sources, including
somatic cell nuclear transfer, parthenogenesis, and/or IVF embryos
created for research purposes, is not eligible for NIH funding.
(2) The NIH is also requesting public comment on the proposed scope
of research (e.g., grant applications, contract proposals, intramural
research protocols, etc.) to be considered by an NIH steering committee
to provide programmatic input to the director of the relevant Institute
or Center (or equivalent NIH official responsible for funding
decisions). The NIH proposes the scope of research include research in
which:
a. Human pluripotent cells are introduced into non-human vertebrate
embryos, up through the end of the gastrulation stage, or
b. human cells are introduced into post-gastrulation non-human
mammals (excluding rodents), such that there could be either a
substantial contribution or a substantial functional
[[Page 51923]]
modification to the animal brain by the human cells.
While the NIH seeks public comment on the proposed changes to the
Guidelines, and on the proposed scope for an NIH steering committee's
consideration of certain research, NOT-OD-15-158 will remain in effect.
Dated: July 28, 2016.
Lawrence A. Tabak,
Deputy Director, National Institutes of Health.
[FR Doc. 2016-18601 Filed 8-4-16; 8:45 am]
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