Abstract
The HLA-C *07:01:01G allele group consists of three nonsynonymous alleles, C *07:01:01, C *07:06 and C *07:18, plus C *07:01:02, which is synonymous to C *07:01:01. All of these alleles have identical exons 2, 3 and 4, but differ in exons 5 or 6. Therefore routine sequence-based typing (SBT) of exons 2 and 3 is unable to resolve these subtypes, resulting in ambiguous typing results in population and disease cohort studies. In the present study, we fully characterized C *07:01:01G subtypes in European and African Americans and examined their relative frequency distributions. In European Americans C *07:01:01G is predominantly represented by C *07:01:01 (94.4%), whereas C *07:01:02 (1.1%) and C *07:18 (4.5%) were detected relatively infrequently. In African Americans C *07:18 (42.4%) showed a high frequency similar to that of C *07:01:01 (44.7%) whereas C *07:06 was detected at a low frequency (4.7%). C *07:06 was found exclusively on B *44:03 carrying haplotypes in both ethnic groups, but C *07:18 showed multiple linkage relationships with HLA-B. These results demonstrate that C *07:01:01G as defined by routine SBT is a heterogeneous group of alleles, especially among individuals of African origin. If C *07:01:01G subtypes prove to bear divergent functional significance, it would be necessary to include these subtypes in routine HLA-C typing for clinical transplantation and disease association studies.
Original language | English (US) |
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Pages (from-to) | 715-719 |
Number of pages | 5 |
Journal | Human Immunology |
Volume | 73 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2012 |
Funding
This project has been funded in whole or in part with federal funds from the National Cancer Institute, National Institutes of Health, under Contract No. HHSN261200800001E. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government. This Research was supported in part by the Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research. This study was supported by the research fund of Guangdong Science & Technology Department (Research Project number: 2008B030301277).
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology