A cluster of nearly 220 genes known as the human leukocyte antigen (HLA) gene complex holds clues to many unsolved medical questions: why do transplants sometimes fail despite close donor-recipient matches? What makes certain people more susceptible to specific diseases? Why do vaccines protect some individuals better than others?
In search of the answers, the National Institutes of Health (NIH) is heading an initiative to catalog the HLA gene complex and explore its differences among populations worldwide. Nearly $20 million over five years will go to the International Histocompatibility Working Group (IHWG), a network of almost 200 laboratories in more than 70 countries, to set up a centralized HLA gene database and develop new and improved tools to decipher this genetic Rosetta Stone of immunology.
John A. Hansen, M.D., at the Fred Hutchinson Cancer Research Center (FHCRC) in Seattle, will lead the project. According to Dr. Hansen, head of FHCRC's Human Immunogenetics Program and a professor of medicine at the University of Washington, the project could have immediate clinical benefits, for example, for finding better matches for bone marrow transplant recipients.
"But the potential impact of these new studies goes way beyond the HLA community immunogenetics," says Dr. Hansen. "This project will apply recent advances in genome technology to important questions about specific diseases and help explain how the rich genetic differences in HLA between individuals can either strengthen the immune response or open the door to autoimmune disease and infection."
The HLA gene complex, known more generally as the major histocompatibility complex (MHC), is responsible for encoding proteins that stud the surface of the body's cells, marking them as our own. Anything not marked as "self" can come under attack from the immune system. This includes foreign matter such as viruses and bacteria as well as cancerous cells and transplanted tissue. Even organs from a close blood relative can display very different HLA markers due to the underlying distinctions within each individual's HLA gene complex; a perfect HLA-type match exists only among identical twins.
The effectiveness of a person's immune defenses for detecting and destroying trespasser antigens depends largely on his or her HLA gene complex. Similarly, these genes are suspected of playing a role when the immune system mistakenly targets the body's own cells as foreign, which is the case with autoimmune disorders such as multiple sclerosis, rheumatoid arthritis and type 1 diabetes. The IHWG will accelerate investigations seeking to discover the fundamental mechanics of how HLA genes direct beneficial and harmful immune responses.
"The IHWG represents more than 30 years of collaborative research among the world's leading scientists in population-based genetics," says Daniel Rotrosen, M.D., director of NIAID's Division of Allergy, Immunology and Transplantation. "Its extensive international network of laboratories will contribute importantly to NIAID's efforts to address the global health problems caused by infectious and immune-mediated diseases."
A primary goal for the IHWG is to create a searchable HLA database linking multiple interacting genes with function, ethnicity and disease. A more centralized database will make it easier for scientists to find and contribute new data. It also will help clinical investigators use the information as a platform for future research on immune-mediated diseases.
Other IHWG objectives include the following:
Knowledge about the patterns of HLA gene combinations prevalent in different ethnic groups also could illuminate the historical relationships among the world's subpopulations. Theoretically, someday scientists could custom-build vaccines based on HLA genes. Such vaccines could provide better protection against diseases endemic to a group or geographic area, such as malaria and the varying subtypes of the human immunodeficiency virus (HIV) appearing in different parts of the world.
For details about IHWG research plans and workshop meetings, visit www.ihwg.org.
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CONTACT: Susan Edmonds
FOR IMMEDIATE RELEASE
Sept. 6, 2000