![]() John A. Hansen, Chair |
![]() Welcome! This newsletter represents the first general communication issued on behalf of the 13th International Histocompatibility Workshop and Conference (IHWC). A tentative date for the 13th IHWC has been set for early in the new millennium in the spring of 2001. Preliminary efforts are now underway to address major planning issues during 1997. The tradition of the International HLA Workshops is strong and compelling. Twelve preceding Workshops have provided powerful opportunity and impetus for major technological and scientific progress. In the interval since the First Workshop hosted by Bernard Amos in 1964, the scope of the Workshop and the number of participating laboratories and individuals worldwide has grown enormously, and the field has witnessed remarkable advances in both fundamental technologies and discoveries. The early accomplishments in the new field of HLA were possible because of the insight of a few pioneering investigators who mastered serology, enabling the identification of novel antigens responsible for inducing leukoagglutinating antibodies in the serum of transfused patients and multiparous women, some of which were capable of causing febrile transfusion reactions. The development of the microcytotoxicity assay, the introduction of computers, the discovery of the mixed lymphocyte culture reaction (MLC) and tissue restricted class II antibodies, and most recently the emergence of molecular methods for defining polymorphism at the genetic level have in their time brought enormous change and progress to the field. From the beginning, biological questions and clinical problems have been the essential motivating factors that continue through the 1990s to inspire our interest in HLA and justify the enormous commitment and effort that underlie HLA workshops. Now as before the value of the Workshop depends on the merit of the scientific questions, the quality of the work, the significance of the findings to our understanding of biology, and their relevance to clinical medicine and public health. Each Workshop has had a central theme and set of goals. To assure that the 13th IHWC succeeds as others before in serving the needs of both established investigators and new laboratories around the world, the emphasis will be on the development of DNA-based typing for HLA class I genes, the dissemination of a standard set of reagents, and the application of this technology to the accurate typing of volunteer hematopoietic stem cell (marrow, cord blood, etc.) donors for the emerging international donor network. Reagents for high resolution typing will also be developed to extend human diversity and disease-association studies initiated in prior Workshops. These efforts to analyze multiple polymorphic genes are important in order to broaden our understanding of the immunobiology of HLA, but also to develop model systems that will be useful in future population-based epidemiology studies aimed at understanding polygenic diseases such as cancer. Recent advances in communications technology, especially the Internet, provide us the opportunity to undertake a highly interactive workshop with real time data submission to the central database and the reporting back to investigators of preliminary results, allele assignments and the identification of potential new variants. Ultimately, the success of our workshop will depend on the close collaboration of many laboratories worldwide willing to donate their time and effort to achieve goals that are of real and practical value to all. We therefore welcome you to the 13th IHWC as we embark on an exciting and challenging project that will carry us forward into the 21st century. |
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Goals of the 13th Workshop |
| Planning for the 13th International Histocompatibility
Workshop and Conference is now underway. Workshop projects, data collection
and data analysis will be conducted over the next four years, culminating in
Workshop and Conference meetings in Seattle in late spring of 2001. The major
goals of the 13th IHWC are to define the extent and nature of HLA class I and
class II genetic diversity and to understand the biological relevance of MHC
variation. This will be accomplished by a Pre-workshop Technology Component
through which standardized reagents for DNA-based typing will be developed,
tested, and distributed to participating laboratories. Reagents and protocols
will be developed for both intermediate and high resolution typing. Development
of intermediate level reagents will be important in the continued transition
from serology to DNA-based typing. Currently, large numbers of volunteer marrow (stem cell) donors are being typed around the world, but experience has shown that there are significant accuracy problems using high volume serology-based typing. Development of a standardized set of reagents for intermediate level DNA-based typing will be an important step toward facilitating a large scale typing effort to increase the pool of unrelated stem cell donors available worldwide. Workshop data will be collected via the Internet, processed through a centralized database, and preliminary results returned to participating laboratories. High-resolution typing of new or interesting workshop samples is anticipated to follow the preliminary analysis. The 13th IHWC will build on the accomplishments of the 12th IHWC whenever possible, and continue to extend the shared HLA allele sequence and frequency database that has been previously established. |
Technology Development
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| A phase I development and feasibility study will take place during
1997/98 as a prelude to the formal Workshop typing activity. The goal of this
"Pre-workshop" study will be to optimize and establish a standard method for
DNA-based class I typing. The class I Pre-workshop will be comprised of two
components: sequence specific oligonucleotide (SSO) typing, and sequencing-based
typing (SBT). The class I Pre-workshop will be organized around two groups of
investigators who are experienced with each method and who are willing to work
together for 12-18 months for the purpose of defining a standard method and a set
of common reagents. A set of class II SSO reagents derived from the HLA-DR, DQ
and DP systems developed in the 11th and 12th Workshops will also be made available.
Although many laboratories are already experienced with high resolution typing for at
least DRB alleles, a common set of reagents for class II will facilitate the
identification of new alleles. It is anticipated that these common SSO reagents will be used by all laboratories. The goal will be to assure that the aims of individual Workshop projects can be met with one set of class I reagents for intermediate level typing (equivalent to current serology) and a second set of high resolution reagents for the identification of alleles. A standard set of workshop reagents is necessary to establish a consistent database that will allow comparison of data between components within the current and future workshops. As genomic typing technology continues to evolve, these standard reagents will provide a uniform and objective framework for building a progressively, site-specific definition of HLA genomic polymorphisms. |