HLA-A1
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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.
A1-B58 haplotype (A1-B17 where B58 is dominant) may remain associated with anti-neutrophil cytoplasmic antibody (ANCA)
A1 in diabetes
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. 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. 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.
Oddly, A1 was also found associated with methotrexate-induced liver cirrhosis. Whereas A1 was found negatively associated with other disease such as coal workers pneumoconiosis and leprosy.
A1 and infectious disease
Within the early studies, A1 was found associate with or protected against some infectious diseases. 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, however, the significance was not consistent. A more recent paper showed an association of A*01:01 with lower than average responses to measles vaccine. With rubella, A1-B8 was more frequently found in people infected as a result of maternal transference. A1 was also found to associate with circumoral herpes. An association between A1 and cold sores was also described. Subsequently, the association for herpes simplex was also shown.
A1 in Lymphoma
In Hodgkin's lymphoma HLA-A1, but DR3 was not found higher. 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.
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Alleles
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.
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-B37 Yakuts, Tribal-India, Iyers-India, Mongolian, Indian, Orochon, Romanian, Yugoslavia, Korean, Albania, French, German, Manchu
- A1-B51 Yugoslavia, Germany, Iberia, Italy
- A1-B52 Bharghavas-India, Tribal-India, Italy, Iberia, France
- A1-B57 (See tables on discussion page)
- A1-B58 (See tables on discussion page)

