International Workshop on Alternatives to the Murine Histamine Sensitization Test (HIST) for Acellular Pertussis Vaccines: State of the Science and the Path Forward, 52333-52334 [2012-21368]
Download as PDF
Federal Register / Vol. 77, No. 168 / Wednesday, August 29, 2012 / Notices
Room 7–A224, 445 12th Street SW.,
Washington, DC 20554). Open
captioning will be provided for this
event. Other reasonable
accommodations for people with
disabilities are available upon request.
Requests for such accommodations
should be submitted via email to
fcc504@fcc.gov or by calling the Office
of Engineering and Technology at 202–
418–2470 (voice), (202) 418–1944 (fax).
Such requests should include a detailed
description of the accommodation
needed. In addition, please include your
contact information. Please allow at
least five days advance notice; last
minute requests will be accepted, but
may be impossible to fill.
AGENCY:
NICEATM also invites
submission of abstracts for scientific
posters for display at the workshop (see
SUPPLEMENTARY INFORMATION).
DATES: The workshop is scheduled for
November 28–29, 2012. Sessions will
begin each day at 8:00 a.m. and will end
each day at approximately 5:45 p.m.
The deadline for registration is
November 16, 2012. The deadline for
submission of poster abstracts is
October 12, 2012.
ADDRESSES: The workshop will be held
at the William H. Natcher Conference
Center, 45 Center Drive, NIH Campus,
Bethesda, MD 20892. Individuals with
disabilities who need accommodation to
participate in this event should contact
Ms. Debbie McCarley at voice
telephone: 919–541–2384 or email:
mccarley@niehs.nih.gov. TTY users
should contact the Federal TTY Relay
Service at 800–877–8339. Requests
should be made at least 5 business days
in advance of the event.
FOR FURTHER INFORMATION CONTACT: Dr.
William S. Stokes, Director, NICEATM,
NIEHS, P.O. Box 12233, Mail Stop: K2–
16, Research Triangle Park, NC, 27709,
(telephone) 919–541–2384, (fax) 919–
541–0947, (email)
niceatm@niehs.nih.gov. Courier address:
NICEATM, NIEHS, Room 2034, 530
Davis Drive, Morrisville, NC 27560.
SUPPLEMENTARY INFORMATION:
The NTP Interagency Center
for the Evaluation of Alternative
Toxicological Methods (NICEATM)
announces an ‘‘International Workshop
on Alternatives to the Murine Histamine
Sensitization Test (HIST) for Acellular
Pertussis Vaccines: State of the Science
and the Path Forward.’’ This workshop,
the third in a series of specialized
vaccine workshops, will review new
methods and approaches for acellular
pertussis (aP) vaccine safety testing that
incorporate innovations in science and
technology. These scientific innovations
should improve test accuracy, precision,
and efficiency while also reducing or
replacing the use of animals in vaccine
safety testing. The goal is to address the
path toward global validation,
acceptance, and implementation of
scientifically valid alternative methods
for aP vaccines.
The workshop is open to the public at
no charge with attendance limited only
by the available space; however,
advance registration is required (see
Background
Pertussis, also known as whooping
cough, is a highly contagious disease
caused by the bacterium Bordetella
pertussis. Pertussis was one of the most
common childhood diseases of the early
20th century and was once a major
cause of childhood mortality in the
United States. A whole-cell vaccine
introduced in the 1940s reduced the
incidence of pertussis by more than
80%. aP vaccines, which became
available in the 1980s, were developed
in response to public concern with some
common side effects (e.g., fever,
swelling at injection site) and rare
serious events that coincided with the
use of whole-cell pertussis vaccines.
These new generation aP vaccines
contain different combinations of the
putative protective antigens of B.
pertussis bacteria (e.g., inactivated
pertussis toxin [PTx/d], pertactin, and
fimbriae) and are less reactogenic than
whole-cell vaccines.
Regulatory authorities require safety,
potency, and purity testing prior to the
release of each production lot of
pertussis or pertussis antigen-containing
vaccines. The murine histamine
sensitization test (HIST) is a key safety
test used to monitor residual levels of
Federal Communications Commission.
Bulah P. Wheeler,
Deputy Manager.
[FR Doc. 2012–21310 Filed 8–28–12; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
International Workshop on Alternatives
to the Murine Histamine Sensitization
Test (HIST) for Acellular Pertussis
Vaccines: State of the Science and the
Path Forward
Division of the National
Toxicology Program (DNTP), National
Institute of Environmental Health
Sciences (NIEHS), National Institutes of
Health (NIH), HHS.
ACTION: Announcement of a workshop;
call for abstract submissions.
TKELLEY on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
17:37 Aug 28, 2012
Jkt 226001
DATES).
PO 00000
Frm 00025
Fmt 4703
Sfmt 4703
52333
pertussis toxin (PTx) in vaccines. This
test is performed to ensure that PTx has
been effectively inactivated before
release of vaccines (Corbel and Xing,
2004). However, such testing may
involve large numbers of mice, some of
which can experience significant
unrelieved pain and distress. In
addition, the HIST has technical
challenges requiring frequent retesting,
thereby increasing vaccine testing
expense and animal usage. An
international workshop organized in
2010 1 by NICEATM, Interagency
Coordinating Committee on the
Validation of Alternative Methods
(ICCVAM), and their international
partners identified the HIST as a
priority for future research,
development, and validation of
alternative test methods that could
further reduce, refine (enhance animal
well-being and lessen or avoid pain and
distress), or replace animal use for aP
vaccine safety testing (Stokes et al.,
2011).
Two international workshops
reviewed currently available alternative
in vitro assays to the HIST and
discussed a path forward to achieve
their validation and adoption 2 3. The
Workshop on Animal-Free Detection of
PTx in Vaccines—Alternatives to HIST
was held on June 9 and 10, 2011, at the
Paul Ehrlich Institute, Germany. An
International Working Group for
Alternatives to HIST (previously
designated as the ‘‘Spiked-vaccine
Working Group’’) was organized to
coordinate future studies on relevant
alternative methods (Bache et al., 2012;
Isbrucker, 2011).
The Alternative Safety Testing
Strategies for Acellular Vaccines
Workshop was held on August 21, 2011,
as a satellite meeting to the 8th World
Congress on Alternatives and Animal
Use in the Life Sciences in Montreal,
Canada (Isbrucker, 2011). Participants at
this workshop further discussed and
clarified regulatory agency requirements
to achieve the acceptance of alternative
methods to the HIST and agreed that
conducting a study using spiked
vaccines to compare the sensitivities of
the HIST and in vitro assays would be
important.
1 International Workshop on Alternative Methods
to Reduce, Refine, and Replace the Use of Animals
in Vaccine Potency and Safety Testing: State of the
Science and Future Directions, Bethesda, MD, USA
September 14–16, 2010.
2 Workshop on Animal-Free Detection of PTx in
Vaccines—Alternatives to HIST, Langen, Germany,
June 9–10, 2011.
3 Alternative Safety Testing Strategies for
Acellular Pertussis Vaccines (8th World Congress
Satellite meeting), Montreal, Canada, August 21,
2011.
E:\FR\FM\29AUN1.SGM
29AUN1
52334
Federal Register / Vol. 77, No. 168 / Wednesday, August 29, 2012 / Notices
Several in vitro assays have been
developed, or are currently under
development, with the aim of finding an
alternative method to the HIST for
monitoring residual PTx activity in aP
vaccines. The International Working
Group for Alternatives to HIST is
coordinating the acquisition and
distribution of aP vaccine samples from
manufacturers to research laboratories
for generation of data using in vitro
methods to evaluate vaccines spiked
with a known amount of PTx. Data from
the various alternative assays will be
presented at the upcoming workshop
and will form the basis for identifying
in vitro methods for future assessment
in the next international collaborative
study.
The following methods will be
evaluated and may be used to generate
data to be presented at the upcoming
workshop:
1. Binding assay: used to assess the
amount of PTx/toxoid binding activity
to the glycoprotein fetuin
2. Enzymatic assay: monitors the
residual ADP-ribosylation of the PTx/
toxoid
3. Cell-based assays: monitor the
generation of cAMP or decrease in
cellular ATP following exposure to
PTx
4. Genetic assays: determine potential
genomic markers of PTx activity
This workshop will provide a forum
to discuss and review the in vitro
protocols and available data from the
International Working Group for
Alternatives to HIST study and will
suggest future collaborative projects
using prepared materials. The workshop
will also review additional new
methods and approaches for aP vaccine
safety testing that should improve test
accuracy, precision, and efficiency
while also reducing or replacing the use
of animals in vaccine safety testing.
Finally, the workshop will address the
path toward global validation,
acceptance, and implementation of
scientifically valid alternative methods
for aP vaccines.
TKELLEY on DSK3SPTVN1PROD with NOTICES
Registration information, draft
agenda, and additional meeting
information are available on the
NICEATM–ICCVAM Web site (https://
iccvam.niehs.nih.gov/meetings/
HISTWksp-2012/HISTWksp.htm) and
upon request from NICEATM (see FOR
FURTHER INFORMATION CONTACT).
NICEATM and ICCVAM invite the
submission of abstracts for scientific
VerDate Mar<15>2010
17:37 Aug 28, 2012
Jkt 226001
Background Information on NICEATM
and ICCVAM
ICCVAM is an interagency committee
composed of representatives from 15
Federal regulatory and research agencies
that require, use, generate, or
disseminate toxicological and safety
testing information. ICCVAM conducts
technical evaluations of new, revised,
and alternative safety testing methods
and integrated testing strategies with
regulatory applicability and promotes
the scientific validation and regulatory
acceptance of testing methods that more
accurately assess the safety and hazards
of chemicals and products and that
reduce, refine, or replace animal use.
The ICCVAM Authorization Act of 2000
(42 U.S.C. 285l¥3) established ICCVAM
as a permanent interagency committee
of the NIEHS under NICEATM.
NICEATM administers ICCVAM,
provides scientific and operational
support for ICCVAM-related activities,
and conducts independent validation
studies to assess the usefulness and
limitations of new, revised, and
alternative test methods and strategies.
NICEATM and ICCVAM welcome the
public nomination of new, revised, and
alternative test methods and strategies
applicable to the needs of U.S. Federal
agencies. Additional information about
ICCVAM and NICEATM can be found
on the NICEATM–ICCVAM Web site
(https://iccvam.niehs.nih.gov).
2011. The International Workshop on
Alternative Methods to Reduce, Refine
and Replace the Use of Animals in
Vaccine Potency and Safety Testing—
Introduction and Summary. In:
International Workshop on Alternative
Methods to Reduce, Refine, and Replace
the Use of Animals in Vaccine Potency
and Safety Testing: State of the Science
and Future Directions (Kulpa-Eddy J,
McFarland R, Stokes WS, eds). Procedia
Vaccinol 5: 1–15.
Dated: August 20, 2012.
John R. Bucher,
Associate Director, National Toxicology
Program.
[FR Doc. 2012–21368 Filed 8–28–12; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–12EK]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
References
Preliminary Workshop Agenda and
Registration
Call for Abstract Submissions
posters to be displayed during this
workshop. Guidelines for the
submission of abstracts are available at
https://iccvam.niehs.nih.gov/meetings/
HISTWksp-2012/HISTWkspAbstractSubmit-508.pdf. Abstracts must
be submitted by email to
niceatm@niehs.nih.gov. The deadline
for abstract submission is October 12,
2012. The corresponding author will be
notified regarding the abstract’s
acceptance within 21 working days of
the submission deadline. Guidelines for
poster presentations will be sent to the
corresponding author with notification
of acceptance.
Proposed Project
Process and Intermediate Outcome
Evaluation of ‘‘Teenage Pregnancy
Prevention: Integrating Services,
Programs, and Strategies through
Community-Wide Initiatives’’—New—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Bache C, Hoonakker M, Hendriksen C,
Buchheit K–H, Spreitzer I, Montag T.
2012. Workshop on Animal Free
Detection of Pertussis Toxin in
Vaccines—Alternatives to the Histamine
Sensitization Test. Biologicals 40: 309–
311.
Corbel MJ, Xing DK–L. 2004. Toxicity and
potency evaluation of pertussis vaccines.
Exp Rev Vaccines 3: 89–101.
Isbrucker R. 2011. Alternative safety testing
strategies for acellular pertussis vaccines.
ALTEX Proceedings, 1/12, Proceedings
of WC8; 77–80.
Stokes WS, Kulpa-Eddy J, McFarland RM.
Background and Brief Description
CDC is currently providing funding to
nine state and community awardees,
and five national organizations, to
examine innovative, evidence-based
teenage pregnancy prevention programs.
Efforts are focused in communities with
high rates of teen pregnancy in underserved African American and Latino
youth. Components of these efforts
include (1) implementing evidencebased or evidence-informed prevention
programs; (2) linking teens to quality
PO 00000
Frm 00026
Fmt 4703
Sfmt 4703
E:\FR\FM\29AUN1.SGM
29AUN1
Agencies
[Federal Register Volume 77, Number 168 (Wednesday, August 29, 2012)]
[Notices]
[Pages 52333-52334]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-21368]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
International Workshop on Alternatives to the Murine Histamine
Sensitization Test (HIST) for Acellular Pertussis Vaccines: State of
the Science and the Path Forward
AGENCY: Division of the National Toxicology Program (DNTP), National
Institute of Environmental Health Sciences (NIEHS), National Institutes
of Health (NIH), HHS.
ACTION: Announcement of a workshop; call for abstract submissions.
-----------------------------------------------------------------------
SUMMARY: The NTP Interagency Center for the Evaluation of Alternative
Toxicological Methods (NICEATM) announces an ``International Workshop
on Alternatives to the Murine Histamine Sensitization Test (HIST) for
Acellular Pertussis Vaccines: State of the Science and the Path
Forward.'' This workshop, the third in a series of specialized vaccine
workshops, will review new methods and approaches for acellular
pertussis (aP) vaccine safety testing that incorporate innovations in
science and technology. These scientific innovations should improve
test accuracy, precision, and efficiency while also reducing or
replacing the use of animals in vaccine safety testing. The goal is to
address the path toward global validation, acceptance, and
implementation of scientifically valid alternative methods for aP
vaccines.
The workshop is open to the public at no charge with attendance
limited only by the available space; however, advance registration is
required (see DATES). NICEATM also invites submission of abstracts for
scientific posters for display at the workshop (see SUPPLEMENTARY
INFORMATION).
DATES: The workshop is scheduled for November 28-29, 2012. Sessions
will begin each day at 8:00 a.m. and will end each day at approximately
5:45 p.m. The deadline for registration is November 16, 2012. The
deadline for submission of poster abstracts is October 12, 2012.
ADDRESSES: The workshop will be held at the William H. Natcher
Conference Center, 45 Center Drive, NIH Campus, Bethesda, MD 20892.
Individuals with disabilities who need accommodation to participate in
this event should contact Ms. Debbie McCarley at voice telephone: 919-
541-2384 or email: mccarley@niehs.nih.gov. TTY users should contact the
Federal TTY Relay Service at 800-877-8339. Requests should be made at
least 5 business days in advance of the event.
FOR FURTHER INFORMATION CONTACT: Dr. William S. Stokes, Director,
NICEATM, NIEHS, P.O. Box 12233, Mail Stop: K2-16, Research Triangle
Park, NC, 27709, (telephone) 919-541-2384, (fax) 919-541-0947, (email)
niceatm@niehs.nih.gov. Courier address: NICEATM, NIEHS, Room 2034, 530
Davis Drive, Morrisville, NC 27560.
SUPPLEMENTARY INFORMATION:
Background
Pertussis, also known as whooping cough, is a highly contagious
disease caused by the bacterium Bordetella pertussis. Pertussis was one
of the most common childhood diseases of the early 20th century and was
once a major cause of childhood mortality in the United States. A
whole-cell vaccine introduced in the 1940s reduced the incidence of
pertussis by more than 80%. aP vaccines, which became available in the
1980s, were developed in response to public concern with some common
side effects (e.g., fever, swelling at injection site) and rare serious
events that coincided with the use of whole-cell pertussis vaccines.
These new generation aP vaccines contain different combinations of the
putative protective antigens of B. pertussis bacteria (e.g.,
inactivated pertussis toxin [PTx/d], pertactin, and fimbriae) and are
less reactogenic than whole-cell vaccines.
Regulatory authorities require safety, potency, and purity testing
prior to the release of each production lot of pertussis or pertussis
antigen-containing vaccines. The murine histamine sensitization test
(HIST) is a key safety test used to monitor residual levels of
pertussis toxin (PTx) in vaccines. This test is performed to ensure
that PTx has been effectively inactivated before release of vaccines
(Corbel and Xing, 2004). However, such testing may involve large
numbers of mice, some of which can experience significant unrelieved
pain and distress. In addition, the HIST has technical challenges
requiring frequent retesting, thereby increasing vaccine testing
expense and animal usage. An international workshop organized in 2010
\1\ by NICEATM, Interagency Coordinating Committee on the Validation of
Alternative Methods (ICCVAM), and their international partners
identified the HIST as a priority for future research, development, and
validation of alternative test methods that could further reduce,
refine (enhance animal well-being and lessen or avoid pain and
distress), or replace animal use for aP vaccine safety testing (Stokes
et al., 2011).
---------------------------------------------------------------------------
\1\ International Workshop on Alternative Methods to Reduce,
Refine, and Replace the Use of Animals in Vaccine Potency and Safety
Testing: State of the Science and Future Directions, Bethesda, MD,
USA September 14-16, 2010.
---------------------------------------------------------------------------
Two international workshops reviewed currently available
alternative in vitro assays to the HIST and discussed a path forward to
achieve their validation and adoption 2 3. The Workshop on
Animal-Free Detection of PTx in Vaccines--Alternatives to HIST was held
on June 9 and 10, 2011, at the Paul Ehrlich Institute, Germany. An
International Working Group for Alternatives to HIST (previously
designated as the ``Spiked-vaccine Working Group'') was organized to
coordinate future studies on relevant alternative methods (Bache et
al., 2012; Isbrucker, 2011).
---------------------------------------------------------------------------
\2\ Workshop on Animal-Free Detection of PTx in Vaccines--
Alternatives to HIST, Langen, Germany, June 9-10, 2011.
\3\ Alternative Safety Testing Strategies for Acellular
Pertussis Vaccines (8th World Congress Satellite meeting), Montreal,
Canada, August 21, 2011.
---------------------------------------------------------------------------
The Alternative Safety Testing Strategies for Acellular Vaccines
Workshop was held on August 21, 2011, as a satellite meeting to the 8th
World Congress on Alternatives and Animal Use in the Life Sciences in
Montreal, Canada (Isbrucker, 2011). Participants at this workshop
further discussed and clarified regulatory agency requirements to
achieve the acceptance of alternative methods to the HIST and agreed
that conducting a study using spiked vaccines to compare the
sensitivities of the HIST and in vitro assays would be important.
[[Page 52334]]
Several in vitro assays have been developed, or are currently under
development, with the aim of finding an alternative method to the HIST
for monitoring residual PTx activity in aP vaccines. The International
Working Group for Alternatives to HIST is coordinating the acquisition
and distribution of aP vaccine samples from manufacturers to research
laboratories for generation of data using in vitro methods to evaluate
vaccines spiked with a known amount of PTx. Data from the various
alternative assays will be presented at the upcoming workshop and will
form the basis for identifying in vitro methods for future assessment
in the next international collaborative study.
The following methods will be evaluated and may be used to generate
data to be presented at the upcoming workshop:
1. Binding assay: used to assess the amount of PTx/toxoid binding
activity to the glycoprotein fetuin
2. Enzymatic assay: monitors the residual ADP-ribosylation of the PTx/
toxoid
3. Cell-based assays: monitor the generation of cAMP or decrease in
cellular ATP following exposure to PTx
4. Genetic assays: determine potential genomic markers of PTx activity
This workshop will provide a forum to discuss and review the in
vitro protocols and available data from the International Working Group
for Alternatives to HIST study and will suggest future collaborative
projects using prepared materials. The workshop will also review
additional new methods and approaches for aP vaccine safety testing
that should improve test accuracy, precision, and efficiency while also
reducing or replacing the use of animals in vaccine safety testing.
Finally, the workshop will address the path toward global validation,
acceptance, and implementation of scientifically valid alternative
methods for aP vaccines.
Preliminary Workshop Agenda and Registration
Registration information, draft agenda, and additional meeting
information are available on the NICEATM-ICCVAM Web site (https://iccvam.niehs.nih.gov/meetings/HISTWksp-2012/HISTWksp.htm) and upon
request from NICEATM (see FOR FURTHER INFORMATION CONTACT).
Call for Abstract Submissions
NICEATM and ICCVAM invite the submission of abstracts for
scientific posters to be displayed during this workshop. Guidelines for
the submission of abstracts are available at https://iccvam.niehs.nih.gov/meetings/HISTWksp-2012/HISTWksp-AbstractSubmit-508.pdf. Abstracts must be submitted by email to niceatm@niehs.nih.gov.
The deadline for abstract submission is October 12, 2012. The
corresponding author will be notified regarding the abstract's
acceptance within 21 working days of the submission deadline.
Guidelines for poster presentations will be sent to the corresponding
author with notification of acceptance.
Background Information on NICEATM and ICCVAM
ICCVAM is an interagency committee composed of representatives from
15 Federal regulatory and research agencies that require, use,
generate, or disseminate toxicological and safety testing information.
ICCVAM conducts technical evaluations of new, revised, and alternative
safety testing methods and integrated testing strategies with
regulatory applicability and promotes the scientific validation and
regulatory acceptance of testing methods that more accurately assess
the safety and hazards of chemicals and products and that reduce,
refine, or replace animal use. The ICCVAM Authorization Act of 2000 (42
U.S.C. 285l-3) established ICCVAM as a permanent interagency committee
of the NIEHS under NICEATM. NICEATM administers ICCVAM, provides
scientific and operational support for ICCVAM-related activities, and
conducts independent validation studies to assess the usefulness and
limitations of new, revised, and alternative test methods and
strategies. NICEATM and ICCVAM welcome the public nomination of new,
revised, and alternative test methods and strategies applicable to the
needs of U.S. Federal agencies. Additional information about ICCVAM and
NICEATM can be found on the NICEATM-ICCVAM Web site (https://iccvam.niehs.nih.gov).
References
Bache C, Hoonakker M, Hendriksen C, Buchheit K-H, Spreitzer I,
Montag T. 2012. Workshop on Animal Free Detection of Pertussis Toxin
in Vaccines--Alternatives to the Histamine Sensitization Test.
Biologicals 40: 309-311.
Corbel MJ, Xing DK-L. 2004. Toxicity and potency evaluation of
pertussis vaccines. Exp Rev Vaccines 3: 89-101.
Isbrucker R. 2011. Alternative safety testing strategies for
acellular pertussis vaccines. ALTEX Proceedings, 1/12, Proceedings
of WC8; 77-80.
Stokes WS, Kulpa-Eddy J, McFarland RM. 2011. The International
Workshop on Alternative Methods to Reduce, Refine and Replace the
Use of Animals in Vaccine Potency and Safety Testing--Introduction
and Summary. In: International Workshop on Alternative Methods to
Reduce, Refine, and Replace the Use of Animals in Vaccine Potency
and Safety Testing: State of the Science and Future Directions
(Kulpa-Eddy J, McFarland R, Stokes WS, eds). Procedia Vaccinol 5: 1-
15.
Dated: August 20, 2012.
John R. Bucher,
Associate Director, National Toxicology Program.
[FR Doc. 2012-21368 Filed 8-28-12; 8:45 am]
BILLING CODE 4140-01-P