DEFECTIVE IMMUNE SYSTEM RESPONSE TO SMALLPOX VACCINE DETAILED IN NEW STUDY

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Institute of Allergy and Infectious Diseases (NIAID)
http://www3.niaid.nih.gov/

EMBARGOED FOR RELEASE: Tuesday, March 21, 2006; 12:00 p.m. ET

CONTACT: Anne A. Oplinger, 301-402-1663, aoplinger@xxxxxxxxxxxxx

DEFECTIVE IMMUNE SYSTEM RESPONSE TO SMALLPOX VACCINE DETAILED IN NEW
STUDY
People with Eczema May Benefit From Finding

Scientists supported by the National Institute of Allergy and Infectious
Diseases (NIAID), part of the National Institutes of Health (NIH), have
identified a defect in the immune response of people with the skin
condition atopic dermatitis that puts them at risk of developing serious
complications following smallpox vaccination. Led by Donald Y.M. Leung,
M.D., Ph.D., of the National Jewish Medical and Research Center in
Denver, the researchers used laboratory-grown human skin cells to show
that an immune system protein called LL-37 is critical in controlling
replication of vaccinia virus, the live virus that is the key component
in standard smallpox vaccine.

The investigators are part of NIAID's Atopic Dermatitis and Vaccinia
Network, which was created in 2004 to integrate clinical and animal
research aimed at reducing the risk of eczema vaccinatum, a potentially
deadly complication of smallpox vaccination. Eczema vaccinatum occurs
almost exclusively in people who have a history of atopic dermatitis, a
common, non-contagious skin disorder also known as eczema.

"This new research, the first to be published by Atopic Dermatitis and
Vaccinia Network scientists, illuminates one potential mechanism leading
to eczema vaccinatum and improves our understanding of the immune
responses to smallpox vaccine of people with atopic dermatitis," says
NIAID Director Anthony S. Fauci, M.D.

Published in this month's issue of "Immunity", the study details how the
overproduction in skin cells of inflammation-promoting molecules called
interleukin-4 and interleukin-13 (IL-4 and IL-13) hampers LL-37 activity
in people with atopic dermatitis. LL-37, a small protein produced in
skin cells, is part of the body's first line of defense against
invaders. Earlier research by Dr. Leung and his colleagues suggested
that LL-37 is critical in controlling the spread of vaccinia virus.

In the current study, the investigators used skin samples taken from
people with atopic dermatitis (as well as samples taken from healthy
volunteers without skin disease and from people with another skin
condition called psoriasis) to further investigate how dysfunctions in
the immune response of people with eczema set the stage for eczema
vaccinatum. When exposed to vaccinia virus, the skin samples from
healthy volunteers and from those with psoriasis reacted by producing
more LL-37. As a result, the replication of the virus was controlled and
eventually halted. In contrast, LL-37 production was minimal in skin
samples from people with atopic dermatitis and vaccinia replication was
poorly controlled. Next, the scientists exposed skin samples from people
with atopic dermatitis to vaccinia, and then added LL-37. With the LL-37
supplement, the skin cells successfully controlled the viral
replication.

Dr. Leung and his group then looked more closely at why vaccinia
infection fails to induce LL-37 production in atopic dermatitis skin.
Comparing immune responses of skin cells grown in the lab from healthy
volunteers and from people with atopic dermatitis, the researchers found
that the latter skin samples produced excessive amounts of IL-4 and
IL-13. Adding IL-4 and IL-13 to skin cells from healthy volunteers prior
to vaccinia exposure reduced levels of LL-37 production. Conversely,
when the scientists applied IL-4- and IL-13-neutralizing antibodies to
skin samples from people with atopic dermatitis, LL-37 production
increased significantly.

Together, these findings suggest a rationale for new treatment
approaches to eczema vaccinatum, notes Dr. Leung. One approach involves
developing drugs to mimic the action of LL-37 or developing
LL-37-containing creams that could be applied to the skin in order to
boost its ability to contain vaccinia virus infection. Another approach
could be to develop agents to neutralize IL-4 and IL-13. Although no
such drugs are currently marketed, compounds that can neutralize IL-4
and IL-13 are under study as possible asthma and allergy treatments, Dr.
Leung says, and might also be applied to eczema vaccinatum treatment.

Smallpox vaccine, which is made with live vaccinia virus (a close
relative of the virus that causes smallpox), has not been routinely
given in the United States since the early 1970s. But recent concerns
about the possibility of a bioterrorist attack using smallpox virus
prompted authorities to reinstate voluntary smallpox vaccination for
specific groups, such as military personnel. In the first five months of
2003, the U.S. Department of Defense vaccinated more than 450,000
personnel against smallpox. During this period, the majority of those
who deferred vaccination cited atopic dermatitis or other skin
conditions as the main reason.

This research also was funded by the National Institute of Arthritis and
Musculoskeletal and Skin Diseases, another NIH component.

News releases, fact sheets and other NIAID-related materials are
available on the NIAID Web site at http://www.niaid.nih.gov.

NIAID is a component of the National Institutes of Health. NIAID
supports basic and applied research to prevent, diagnose and treat
infectious diseases such as HIV/AIDS and other sexually transmitted
infections, influenza, tuberculosis, malaria and illness from potential
agents of bioterrorism. NIAID also supports research on transplantation
and immune-related illnesses, including autoimmune disorders, asthma and
allergies. 

The National Institutes of Health (NIH) -- "The Nation's Medical
Research Agency" -- includes 27 Institutes and Centers and is a
component of the U.S. Department of Health and Human Services. It is the
primary federal agency for conducting and supporting basic, clinical and
translational medical research, and it investigates the causes,
treatments, and cures for both common and rare diseases. For more
information about NIH and its programs, visit http://www.nih.gov.
 
--------------------------------------------------
Reference: MD Howell et al. Cytokine milieu of atopic dermatitis skin
subverts the innate immune response to vaccinia virus. "Immunity" DOI:
10.1016/j.immuni 2006.02.006 (2006). 
--------------------------------------------------

##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/mar2006/niaid-21b.htm.

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