NHLBI Working Group
Needs and Opportunities to Study Hypersensitivity Pneumonitis
Executive Summary
Full text of the published
article is now available.
The National Heart, Lung, and Blood Institute in collaboration
with the Office of Rare Diseases convened a Working Group on May
10-11, 2004, in Bethesda, Maryland to identify the opportunities
for scientific advancement in Hypersensitivity Pneumonitis (HP).
The Working Group participants discussed the current disease definition,
methods to establish the diagnosis, occupational exposures, animal
models, immunology, and host risk factors. It was recognized by
the Working Group, that despite its putatively low prevalence,
the impact on individuals of all ages continues to be a major
health risk. Furthermore, the lack of recognition and limited
understanding of the mechanisms of the disease have fostered development
of chronic cases whom in general have been exposed to low levels
of antigen for prolonged periods. Although removal from exposure
may provide partial improvement, the overall treatment alternatives
are limited. The group reviewed the current status of HP research
and from these discussions provided the Institute with recommendations
for new research opportunities to improve the accuracy of clinical
diagnosis and investigate mechanisms.
The general recommendations of the Working Group are to:
- Establish a multi-center collaboration to enhance the understanding
of the disease, including a tissue and radiographic repository to assist
in the characterization of the disease.
- Define the natural history of the disease in the context of other
lung diseases such as asthma and COPD. There is a need for better criteria
for diagnosis.
- Use of circulating mononuclear cells or lymphocyte subsets isolated
from peripheral blood in research may provide additional information
to establish the diagnosis.
- Develop population-based studies, particularly in settings where
the disease is endemic to provide additional insights for uniformity
in environmental and clinical characterization of such cases.
- Use of minimally invasive biomarkers (e.g. nasal lavage, induced
sputum, exhaled breath condensates, etc) in the diagnosis of the disease.
- Develop a battery of standardized antigens for diagnosis and make
them available to clinicians.
- Use of quantitative and qualitative CT in prospective evaluation
and longitudinal follow-up studies of HP and other organic dust diseases.
- Conduct genetic studies in the context of gene-environment interaction
to better understand host risk factors.
Working Group Members
Chair: Jordan N. Fink, M.D., Medical College of Wisconsin
Members
- Yves F. Cormier, M.D., Hospital Laval, Canada
- Leland L. Fan, M.D., Texas Children's Hospital
- Teri J. Franks, M.D., Department of Pulmonary and Mediasyinal Pathology
- Kay Kreiss, M.D., National Institute for Occupational Safety and Health
- Steven Kunkel, Ph.D., University of Michigan Medical School
- David Lynch, M.D., MBBS, University of Colorado Health Science Center
- Santiago Quirce, M.D., Ph.D., Fundacion Jimenez Diaz, Alergia, Spain
- Cecil Rose, M.D., MPH, National Jewish Medical Research Center
- Robert Schleimer, Ph.D., Johns Hopkins University
- Mark R. Schuyler, M.D., VA Medical Center, Albuquerque, New Mexico
- Moises Selman, M.D., Inst. Nat. Enfermedades Resp., Mexico
- Douglas Trout, M.D., National Institute for Occupational Safety and
Health
- Yasayuki Yoshizawa, M.D., Tokyo Dental and Medical University, Japan
NHLBI Staff
- Hector Ortega, M.D., Sc.D., Division of Lung Diseases
- Herbert Reynolds, M.D., Division of Lung Diseases
July 2004
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