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Medical Genomics of the Human Immune System For PMK Medical Student Y3

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Page 1: Genetic Disorders of the Human Immune System · 7/24/2019  · Gene Structure of the Human MHC Chromosome 6p21.3 ... Ig H Chain Gene Rearrangements IGH@ 14q32 Somatic rearrangement

Medical Genomics of the

Human Immune SystemFor PMK Medical Student Y3

Page 2: Genetic Disorders of the Human Immune System · 7/24/2019  · Gene Structure of the Human MHC Chromosome 6p21.3 ... Ig H Chain Gene Rearrangements IGH@ 14q32 Somatic rearrangement

Content

B1.4.7 Immunogenetics: MHC structure and function,

erythrocyte antigens

B1.5.5 Diseases of the immune system

I. Molecular Immunogenetics

II. Clinical Immunogenetics

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I. Molecular Immunogenetics

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Innate ImmunityNon-specific responses such as phagocytosis

Adaptive ImmunitySpecifically acquired T and B lymphocytic responses

to particular antigens

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Genes of Key Components of the

Adaptive Immune Response

• Major Histocompatibility Complex (MHC)

• Immunoglobulin (Ig)

• T-Cell Antigen Receptor (TCR)

“ Immunoglobulin gene superfamily ”

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MHC Class I Mediated Antigen

Presentation

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MHC Class II Mediated Antigen

Presentation

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Gene Structure of the Human MHC

Chromosome 6p21.3

Class I + II → Classical HLA

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Major Histocompatibility Complex

MHC region:

o The MHC genomic region, located on the short arm of

chromosome 6 (6p21.3)

o Contains the HLA (Human Leukocyte Antigen) genes

o At least 200 other genes (≈40% involved in some aspect of the

immune response)

o Spanning ≈ 3.6 Mb (Shiina et al, 2009)

o It is the most gene-dense region of the genome (≈ 1 gene/16 kb)

o High levels of polymorphism

o Referred to as the HLA region (in humans)

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Extended MHC region:

o ≈ 8 Mb of chromosome 6, containing over 250

protein-coding genes

o This region expands the MHC borders to

segments with high linkage disequilibrium with the

MHC

o Contains additional genes involved in the immune

response (Horton et al, 2004; Shiina et al, 2009)

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Major Histocompatibility Complex

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MHC / HLA Class

• Class or loci of HLA genes:

oClassical HLA genes are the highly

polymorphic loci that code for the proteins that

present peptides to the T-cell receptors (HLA-

A, -B, -C, -DPA1, -DPB1, -DQA1, -DQB1, -

DRB1, -DRA1) → Class I, II

oNon-Classical genes which have reduced

polymorphism and do not have a role in

peptide presentation. → Class III

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Class III is not HLA

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HLA allele

o A specific DNA sequence at an HLA gene

oCan be thought of as a haplotype of SNP

variants

o There are extraordinarily large numbers of

HLA alleles, with > 12,000 for class I alleles

and > 4,000 for class II.

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HLA Haplotype

The combination of alleles at several HLA genes

on a single chromosome of a given individual.

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Protein & DNA Variation at HLA Loci

HLA Locus Antigenic Variants DNA Variants

HLA-A 25 83

HLA-B 53 186

HLA-C 11 42

HLA-DR 20 221

HLA-DQ 9 49

HLA-DP 6 88

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HLA Function

• HLA class I molecules

o Expressed in most cells, bind peptides of intracellular origin and present

them on the cell surface to the TCRs of CD8+ T-cells

o Initiating a cytotoxic response if they are recognized as foreign.

• HLA class II molecules

o Expressed in antigen presenting cells, typically bind peptides of extracellular

origin and present them to the TCRs of CD4+ T-cells

o Triggering a signaling process that leads to the multiplication of T-helper

cells

o Leading to the stimulation of B-cells, which produce antibodies to the

antigen that triggered the response.

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Inheritance of HLA Haplotypes

AB CD

AC BD AD BC

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HLA Allele & Diseases Associations

Ankylosing spondylitis B27

Reiter syndrome B27

Acute anterior uveitis B27

Nacrolepsy DQ6

Celiac disease DQ2

Hemochromatosis A3

Congenital adrenal hyperplasia Bw47

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Nomenclature of HLA Allele

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N = Null

L = Low

S = Secreted

C = Cytoplasm

A = Aberrant

Q = Questionable

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Immunoglobulin

(Ig)

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Ig H Chain Gene Rearrangements

IGH@

14q32

Somatic rearrangement

Somatic rearrangement

(recombinases)

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Ig L Chain Gene Rearrangements

IGK@

2p12

Note: λ L chain gene

is IGL@ on 22q11

(recombinases)

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Restricted Expression

• Isotypic exclusion

Ig produced by single B cell contains only

a single H isotype and a single L isotype

• Allelic exclusion

Either the paternal or maternal allele for

each H and L chain is expressed within

single cell

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Generation of Antibody Diversity

Germline Genes H κ λ

V 200 100 100

D 20 - -

J 6 5 6

V x D x J 2.4x104 500 600

H x κ 1.2x107

H x λ 1.4x107

Total potential ~1011

repertoire7/24/2019 Col Kitti Buranawuti, MD, FACMG 28

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Immunoglobulin Diversity

• Unique somatic rearrangement of DNA

sequence in lymphocyte precursor cells

• Can generate ~ 1011 different antibodies

• Protect against the large array of

infectious organisms, toxins, cancer cells

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T Cell Receptor

(TCR)

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T Cell Receptor Genes

TRB@ Chromosome 7q34

TRG@ Chromosome 7p14

TRA@ and TRD@ Chromosome 14q11.2

TRD@

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ABO Red Cell Antigen

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ABO gene

• Chromosome: 9q34.2

• ABO gene is organized in 7 exons

• Spans over 19 kb

• Base pairs: 1,147

• Amino acids: 373

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ABO Alleles• O blood: deletion of guanine 258 near the N-terminus of the protein

which results in a frameshift and translation of an almost entirely

different protein

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• A, B blood:

o The first of the seven nucleotide

substitutions which distinguish the

A and B transferases, resides in

coding exon 6; exon 7 contains the

other 6 nucleotide substitutions which

result in four amino acid substitutions

that differentiate the A and B

transferases.

o Among those, substitutions

responsible for alterations at two sites

(L266M and G268A) determine the A

or B specificity of the enzyme

(Yamamoto and Hakamori).

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II. Clinical Immunogenetics

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SCID Genetic Analysis Today

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SCID Genes

T B NK

• IL2RG XL 50% - + -

• ADA AR 14% - - -

• JAK3 AR 7% - + -

• IL7RA AR 7% - + +

• RAG AR <7% - - +

• ARTEMIS AR <5% - - +

• CD45 AR rare - + +

• TCRD (CD3δ) AR rare - + +

• FOXN1 AR rare - + +

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Gene Therapy for the Treatment of Primary Immune

Deficiencies. Kuo CY, Kohn DB

Curr Allergy Asthma Rep. 2016 May;16(5):39.

Gene Therapy for X-Linked Severe Combined Immunodeficiency:

Where Do We Stand?

Cavazzana M, Six E, Lagresle-Peyrou C, André-Schmutz I

Hum Gene Ther. 2016 Feb;27(2):108-16.

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Thank You & Good Luck !

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