HLA-A68

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major histocompatibility complex (human), class I, A68
Alleles	A*6801 A*6802 A*6803 A*6804 A*6805
Structure (See HLA-A)
Identifiers	6801 6802 6803 6804 6805
Symbol(s)	HLA-A
EBI-HLA	A*6801
EBI-HLA	A*6802
EBI-HLA	A*6803
EBI-HLA	A*6804
EBI-HLA	A*6805
Shared data
Locus	chr.6 6p21.31

HLA-A68 (A68) is an HLA-A serotype. The serotype is a split antigen serotype also recognized by the broad antigen serotype A28. The closely related A*6901 is derived, by recombination from A68.

Contents 1 Serotype 2 Disease Associations 2.1 By allele 3 Allele freqeuncies 3.1 A*6801 3.2 A*6802 3.3 A*6803 3.4 A*6805 4 A68 haplotypes 4.1 Indigeonous American haplotypes 4.2 Old World A68 haplotypes 5 References

[edit] Serotype

A68, A28, and A69 serotype recognition of Some HLA A*68 allele-group gene products^[1]

A*68	A68	A28	A69	Sample
allele	%	%	%	size (N)
6801	27	63		2736
6802	19	72	1	2327
6803	28	63		202
6804	17	52		6
6805	29	53		59

[edit] Disease Associations

[edit] By allele

A*68 is associated with higher viral load in HIV^{[2] [3]}. A68 may be protective against symptomatic heart disease in Chaga's cardiomyopathy.^[4]

[edit] Allele freqeuncies

A68 can be subdivided into 3 alleles, *6801, *6802, *6803. *6801 can also be subdivided into *680101 and *680102 (previously called *68011 and *68012).

[edit] A*6801

A*6801 is higher in certain Native American groups, South Asian peoples, African peoples, however *6801 is at low levels in most of SE Asia, particularly the indigeonous populations. This is also reflected by low levels along the West Pacific Rim including Japan. The hiatus of *6801 breaks in Northern Japan with the 3% frequency found in the Ainu, which continues to increase with Arctic peoples and and falls of in Native Americans. Whereas in the Western Eurasia's northern regions, A*6801 falls off. In both Africa and the New World both A*680101 and A*680102 can be found.^[5] Although in the New World A*680102 is more prevalent.

[edit] A*6802

HLA A*6802 frequencies

		freq
ref.	Population	(%)
[6]	Yucpa (Venezuela)	37.2
[7]	Nandi (Kenya)	11.6
[8]	Kenya	10.5
[9]	Harare Shona (Zimbabwe)	9.8
[10]	Natal Zulu (S. Africia)	9.5
[7]	Luo (Kenya)	7.6
[7]	Mali Bandiagara	6.2
[5]	Sudanese	5.5
[7]	Kampala (Uganda)	5.2
[11]	Baka Pygmy (Cameroon)	5.0
[12]	Mestizos (Guadalajara,Mexico)	4.9
[13]	SEastern Isl (Cape Verde)	4.8
[14]	Nador Metalsa (Morocco)	4.8
[5]	Chiriguanos (Argentina)	4.7
[15]	Mossi (Burkina Faso)	4.7
[7]	Lusaka (Zambia)	4.7
[11]	Bamileke (Cameroon)	4.5
[5]	Sawa (Cameroon)	3.8
[5]	Kalash (Pakistan)	3.3
[5]	Beti (Cameroon)	3.2
[5]	SE France	3.1
[5]	Seri (Sonora,Mexico)	3.0
[5]	Yaounde (Cameroon)	2.8
[5]	Tunisia	2.5
[5]	Guinea Bissau	2.3
[5]	Fulani (Burkina Faso)	2.0
[5]	S. Portugal	2.0
[5]	Oman (E. Arabia)	1.7
[5]	Corsica (France)	1.6
[5]	Baloch (Pakistan)	1.6
[5]	Niokholo Mandenka (Senegal)	1.6
[5]	Eastern Andalusia (Spain)	1.5
[5]	Orkney (Scotland)	1.4
[5]	Mestizos (Mexico)	1.2
[5]	Baloch(Iran)	1.1
[5]	Bergamo (Italy)	1.1
[5]	Northern Han (China)	1.0
[5]	Central Portugal	1.0
[5]	Czech Republic	0.9
[5]	Northern Ireland	0.9
[5]	Jews (Israel)	0.9
[5]	Mixe (Oaxaca,Mexico)	0.9
[5]	Madeira (Spain)	0.8
[5]	Cayapa (Ecuador)	0.6
[5]	Svans (Georgia)	0.6
[5]	Majorca/Minorca (Spain)	0.6
[5]	Belgium	0.5
[5]	Lakota (Sioux)	0.5

A*6802 has a global node within certain native peoples of South America, at 37%. A secondary node can be found in Africa. Like *6801 there is an hiatus of *6802 in SE Asia's indigeonous populations, indicating that this population is not a likely source within the native peoples of the New World. Levels are generally low (<1%) in Europe except along the Mediterranean coast. In Africa, higher levels can be found in Kenya and in Western Africa and the Cape Verde Islands.^[5] A note on purity, the notion that A*6802 is of indigeonous native American origin can be challenged based on possibility of introgression from Europeans and Africans. In the case of the Yucpa this is not teneble. The Yucpa have an HLA-DQ8 frequency of ~80%, the highest DQ allele frequency in the world, this tribe shows little evidence of European genetic introgression, in addition the closest DQ8 frequency in terms of Africa are the isolated !Kung of Namibia. There are two possible sources of A*6802: Africa direct and Africa via Asia. The associated B alleles (B*48, B*61) point toward and Asian origin or an African source of very ancient origin, since time would be required to recombine Asian typical B alleles with A68. In the Spanish, A28 levels are 3.1% of this ~0.5% is A*6901, A*6802 is about 2.0% which means the net level of A*6802 to A*6805 in the Spanish is ~0.5%. Of 11 NA groups surveyed 9 are above and 2 are below 0.5%. Of the two Spanish groups 1 (Andalusia - 1.5%) is above and the other (Catalon 0.0%) is below. In an admixture model Spanish introgression does not explain A*6802 in the New World. The Asian model of migration shows no single people NE of Pakistan that has A*6802.

[edit] A*6803

HLA A*6803 frequencies

		freq
ref.	Population	(%)
[16]	Mayan (Guatemala)	7.6
[17]	Bakalo pygmy (Cameroon)	6.0
[12]	Mestizo (Guadalahara Mexico)	3.9
[18]	Mestizo (Mexico)	3.7
[17]	Mbenzele Pygmy (Central African)	1.5
[19]	Lakota (Souix)	1.2
[20]	Yupik (Eskimo-Alaska)	1.0
[9]	Buriat (Mongolia)	0.4
[9]	N. Ireland, Romania, Czech,	0.0

A*6803 can be found in native peoples of the New World and in Central Asia, in Africa it appears to be limited to West and Central Africans. This distribution along with the information on 6801 and 6802 suggests a probable redistribution of *68 alleles from Africa after the initial migration from East Africa that colonized Southeast Asia. It also provides support for 2 waves of migration from Asia to the New World or, at minimum, an unknown mixing area of West Pacific Rim haplotypes and West African/Middle Eastern derived haplotypes in Eastern Asia before the first migration. At present the incursion of Western Eurasian peoples into East Asia follows evidence for reuse of transbiakal region after 18,300 years and correlates with the insipient Jomon period of Japan several thousands of years later. Certain alleles and haplotypes of HLA in South Americans target Japans estimated pre-Yayoi composition, but other peoples, for example in western Mexico are most similar to the Ainu and the peoples of the Amur basin.

[edit] A*6805

A*6805 is found in the Guatemalan and Central African Mbenzele at low levels.

[edit] A68 haplotypes

The genetic distance between Native Americans and Eurasians is too great for the persistence of shared haplotypes, particularly in light of the lower levels in most of Siberia. The link of haplotypes with Western Africa may be significant, and may indicate a rapid eastward migration and admixing within the late paleolithic period.

[edit] Indigeonous American haplotypes

A*680102-B35 haplotypes

• A*680102 Cw*0304 B*3506 (A68-Cw10-B35)
• A68-Cw4-B35 (Terena, Seri (Mexico))
  • A*680102 Cw*0401 B83521 (A68-Cw4-B35) (Terena)

A*6802-B35

• A*6802-B3501 Guadalahara.
• A*6802-B3502 Guadalahara.

A68-B35 Mayan (A*6803).

These two haplotypes are consistent with the presence of Cw4-B35 and A68 in Asia and Middle East and A68-B35 maybe the ancestral A68 haplotype. A28(A*6802)-B35 is found in Senegal.^[21]

A6801-B4002/4 - Terena, Eskimo, Mestizo, Tribal Indians (Asia)

A*680102-B*520102 in the Mexican Mestizo population. A28(A*6802)-B52 is also found in Senegal.^[21]

[edit] Old World A68 haplotypes

A28(~A68)-B51 Armenia, Senegal, Eskimo ^[21]
A28(~A68)-B70 W. Afr, Zaire, Zimbabwe, N. and S. African (Non-caucasians), Khoi (Hottentot)^[21]

[edit] References

v • d • e HLA-A serotypes HLA-A · A1 · A2 · A3 · A9 (A23 · A24) · A10 (A25 · A26 · A34 · A43 · A66) · A11 · A19 (A29 · A30 · A31 · A32 · A33 · A74) · A28 (A68 · A69) · A36 · A80