HLA-A1 (A1) is a human leukocyte antigenserotype within HLA-A "A" serotype group. The serotype is determined by the antibody recognition of α1 subset of HLA-A α-chains. For A1, the alpha "A" chain are encoded by the HLA-A*01 allele group and the β-chain are encoded by B2Mlocus.[1] This group currently is dominated by A*01:01. A1 and A*01 are almost synonymous in meaning. A1 is more common in Europe than elsewhere, it is part of a long haplotype that appears to have been frequent in the ancient peoples of Northwestern Europe. A1 is a frequent component of the AH8.1 haplotype.
A1 serotype positivity is roughly linked to a large number of inflammatory diseases and conditions believed to have immune system involvement. Because of its linkage within the AH8.1 haplotype many studies showed association with A1 or A1,B8 only later to show the association drift toward the class II region gene alleles, DR3 and DQ2.5. While it is not clear what role A1 has in infectious disease, some linkage with infection rates in HIV remain associated within the A1 region of the haplotype.
In all instances so far, HLA-A1 has been found to be linked to disease by association, but there are few that define HLA-A1 has a predominant genetic risk relative to other gene-alleles in the vicinity of the A1 gene on the larger haplotype.
A1 and autoimmune diseases
A1 serotype was associated with a number of diseases as "HL-A"' antigens were first being described. The associations rapidly expanded to include 'HL-A8' HLA-B8, as the HLA A1 and B8 were found to be commonly linked. As DRw3 was characterized, autoimmune risk drifted toward the class II region.
With the exception of type 1 diabetes, most of the evidence for direct association of A1 with autoimmune diseases evaporated as DR3 and DQ2 genes were characterized. While type 1 diabetes shows an extended association on the HLA A1-B8-DR3-DQ2 haplotype, the association appears not to extend beyond the HLA-B locus.[4] A recent study of DR3-DQ2/DR4-DQ8 phenotype found that A1-cw7-B8 was actually lower than expected relative to other A-B types, indicating that risk associated genes are located between B8 and DR3. However a study elsewhere showed that A*01:01 appears to alter risk for type 1 diabetes but not Cw7-B8.[5] The type 1 diabetes example shows the inherent difficulty in the use of linkage analysis alone to cipher risk.
A1 and allergic disease, sensitivities
Early in the study of HLA an association was found between HL A1,B8 in allergic disease, these are found to link to extended HLA A1-B8 region.
Within the early studies, A1 was found associate with or protected against some infectious diseases.[10][11][12] Some diseases found associated with A1 actually link to the extended A1-B8 haplotype, viral induced hepatitis and accelerated progression of HIV are examples.
A1 with B8 showed an increase risk of measles infection,[13] however, the significance was not consistent.[14] A more recent paper showed an association of A*01:01 with lower than average responses to measles vaccine.[15] With rubella, A1-B8 was more frequently found in people infected as a result of maternal transference.[16]
A1 was also found to associate with circumoral herpes.[10] An association between A1 and cold sores was also described.[17] Subsequently, the association for herpes simplex was also shown.[18]
A1 in Lymphoma
In Hodgkin's lymphoma HLA-A1,[19] but DR3 was not found higher.[20] The A1-B8-DR3-DQ2 haplotype has a known association with Enteropathy-associated T-cell lymphoma, approximately 70% of patients are homozygotes for DQ2 with at least one copy of DR3-DQ2.
Most of the disease risk conferred by A*01:01 are represented by either A1 serotype risks, or A1-B8 serotype risk (In Europe A1-B8 is almost always composed of A*01:01 and B*08:01). The other alleles, A*01:02 and A*01:03, may confer specific risks. For example, A*01:02 was found linked to a type of stroke seen frequently in children with sickle cell anemia.[22]
There is a report that in the Somali communities within the US 2/3 of A1 bearers have the A*01:03 isoform.
A1-B haplotypes
A1-B8 Western Irish, N. Irish, Scottish, Wales, NW England, Scandinavia, Yugoslavia, Russia,....
A1-B7 Armenia, Austria, NW Europe (regional recombinant between A1-B8 and A2/A3-B7)
A1-B13 Uralic
A1-B35 (Albania, Belgium, Italy, Greece, France - Eastern Mediterranean in origin)
A1-B52 Bharghavas-India, Tribal-India, Italy, Iberia, France
A1-B57 (See tables on discussion page)
A1-B58 (See tables on discussion page)
References
^Arce-Gomez B, Jones EA, Barnstable CJ, Solomon E, Bodmer WF (February 1978). "The genetic control of HLA-A and B antigens in somatic cell hybrids: requirement for beta2 microglobulin". Tissue Antigens. 11 (2): 96–112. doi:10.1111/j.1399-0039.1978.tb01233.x. PMID77067.
^Wagner MM, Darke C (August 1979). "HLA-A and B antigen frequencies in Welsh coalworkers with pneumoconiosis and Caplan's syndrome". Tissue Antigens. 14 (2): 165–8. doi:10.1111/j.1399-0039.1979.tb00834.x. PMID91226.
^Heise ER, Mentnech MS, Olenchock SA, et al. (June 1979). "HLA-A1 and coalworkers' pneumoconiosis". Am. Rev. Respir. Dis. 119 (6): 903–8. PMID453710.
^Heise ER, Major PC, Mentnech MS, Parrish EJ, Jordon AL, Morgan WK (September 1975). "Predominance of histocompatibility antigens W18 and HL-A1 in miners resistant to complicated coalworkers pneumoconiosis". Inhaled Part. 4 Pt 2: 495–507. PMID1236236.
^Hug G (May 1976). "Genetic factors and autoimmunity in viral hepatitis". Am. J. Clin. Pathol. 65 (5 Suppl): 870–5. PMID218441.
^Honeyman MC, Dorman DC, Menser MA, Forrest JM, Guinan JJ, Clark P (February 1975). "HL-A antigens in congenital rubella and the role of antigens 1 and 8 in the epidemiology of natural rubella". Tissue Antigens. 5 (1): 12–8. doi:10.1111/j.1399-0039.1975.tb00520.x. PMID1138435.
^Ovsyannikova IG, Ryan JE, Vierkant RA, Pankratz VS, Jacobson RM, Poland GA (December 2005). "Immunologic significance of HLA class I genes in measles virus-specific IFN-gamma and IL-4 cytokine immune responses". Immunogenetics. 57 (11): 828–36. doi:10.1007/s00251-005-0061-6. PMID16331510. S2CID25508939.
^Hansen JA, Young CW, Whitsett C, et al. (1977). "HLA and MLC typing in patients with Hodgkin's disease". Prog. Clin. Biol. Res. 16: 217–27. PMID143667.
