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Thread: Race Differences in Immune Genes

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    Lightbulb Race Differences in Immune Genes

    Researchers have found the behaviour of immune system genes varies from race to race - potentially affecting how they respond to infection.

    The Chicago University team looked at over 9,000 genes in 180 people, half Caucasian and half from Nigeria.

    They found differences between the two races in 5% of key genes.

    The American Journal of Human Genetics study may help explain why some groups are more vulnerable to disease, and aid development of more tailored treatment.

    The researchers used gene chip array technology, which uses a microscope to analyse a specialised slide capable of containing thousands of genes derived from blood cells.

    Sixty nuclear families, each including a mother, a father and a child were studied. Thirty were from Utah in the US, while the rest were Yorubans from Ibadan, Nigeria.

    The researchers looked at expression levels - how active a gene is.

    They found significant differences, particularly in immune system genes involved in producing antibodies to combat bacterial infection.

    This backs up previous work which has shown African Americans may be more susceptible than Caucasians to infection, such as the gum disease bug Porphyromonas gingivalis.

    The US study also found activity levels varied significantly in genes involved in basic cellular processes which are thought to play a part in how the body responds to drugs, including the risk of side effects.

    Professor Eileen Dolan, who led the research, said: "Our primary interest is the genes that regulate how people respond to medicines, such as cancer chemotherapy.

    "We want to understand why different populations experience different degrees of toxicity when taking certain drugs and learn how to predict who might be most at risk for drug side effects."

    She added: "Population differences in gene expression have only recently begun to be investigated.

    "We believe they play a significant role in susceptibility to disease and in regulating drug response.

    "Our current research focuses on how these genetic and expression differences play a role in sensitivity to adverse effects associated with chemotherapy."

    Dr Chris Tyler-Smith, a geneticist at the Wellcome Trust's Sanger Institute, said genetic differences between ethnic groups were "small and subtle".

    "They usually just consist of slight differences in frequency of a few variants found in all populations. But they are important for our understanding of recent evolution and can have medical implications as well.

    "They have been difficult to identify, and it is particularly interesting to see that characteristics like variation in susceptibility to infection are showing up."

    Source: http://news.bbc.co.uk/2/hi/health/7270562.stm

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    Here is why;

    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3677943/

    In a nutshell, it is the human leukocyte antigen system HLA). Most people think this and this alone is the immune system but it is the secondary immune response after the bacterial system we contain in our intestines. Nevertheless, the HLA system is super-important and varies racially. Besides whatever basic system we inherited as members of the genius Homo, we all got some allelic variants from Africa. But, in addition to the African HLA system, non-Africans inherited four variants from the Neanderthals and four additional variants from the Denisvans. So people in western Eurasia have Neanderthal variants and people in Oceania and East Asia have Denisovan variants in addition to the African ones which came with Homo sapiens. These are given number and letter designations, so there are HLAa, HLAa1, HLAc and so on. The interesting thing is after they introgressed to us, some of these variants rose to high frequency 20-30% is not uncommon. In some Pacific regions there are 90% figures and even in East Asia, percentages of Denisovan derived alleles is very high.

    Another point, not only does this difference result in differing immunity to disease, it can not help but result in differing responses to vaccination.

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