department of immunology november, 2008
DESCRIPTION
Immune system and its function benefit x damage defense immune surveillance toleranceTRANSCRIPT
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Imunodeficiencies
Department of ImmunologyNovember, 2008
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Immune system and its function benefit x damage defense immune surveillance tolerance
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Immune system and its function
repeated infections pathological reaction to
environmental antigens pathological reaction to
internal antigens defects in immune
immunodeficiencies
allergy
autoimmunity
tumours
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Immune system and its function
repeated infections pathological reaction to
environmental antigens pathological reaction to
internal antigens defects in immune
immunodeficiencies
allergy
autoimmunity
tumours
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Common defense mechanisms
skin and mucosa
cilia, mucus
hydrochloric acid
flow of urine
tears
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Roles of immune system components
innate immunity humoral - complement
cellular - phagocytes, NK cells
adaptive immunity humoral - antibodies
cellular - T lymphocytes
defense against bacteria, some viruses
bacteria, fungi
extracelullar bacteria viruses
intracelullar bacteria viruses, fungi
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Role of immune systemin infection combat
0102030405060708090
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bact
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Vir
uses
Fung
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Intr
acel
lula
rba
cter
ia
PhagocytesNK cellsB cellsCD4+ T cellsCD8+ T cells
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Immunodeficiencies 1. primary
• innate diseases • genes coding for immune system
components
2. secondary • secondary immune disorders based on
primary cause
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Secondary immunodeficiency= presence of underlying disease
malignancy (malignancy) infection (e.g. HIV) malnutrition immunosuppresive drugs
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Classification of primary immunodeficiencies
Antibody• agammaglobulinaemia• hypogammaglobulineamia• deficit of specific antibodies• deficit of isotype switch
Cellular, combined• severe combined (SCID)
• cytokine signalization• T-cell receptor signalization• recombination of T-cell receptor genes• purine metabolism• expression of HLA molelules
• combined• intercelluar signalization• intracellular signalization • cellular motility• chemokine signalization• transcription factors• IFN gamma/IL-12 pathway
Phagocyte number of phagocytes adhesion function (intracellur killiing)
Complement particular components regulatory factors
Malfunction of regulation cytotoxicity negative feedback apoptosis
Syndromes with compromised DNA repair
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Prevalence of primary immunodeficiencies (PID)
70%
1%
20%
9%
humoral
cellular andcombinedphagocytic
complement
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Incidence of PID (examples) sIgAD 1 : 500 - 700
DGS 1 : 4.000 (live births) CVID 1 : 10.000 – 50.000 SCID 1 : 100.000
CD19 deficit only a few cases
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Differentiation of B and T cells
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Classification of primary immunodeficiencies
Antibody• agammaglobulinaemia• hypogammaglobulineamia• deficit of specific antibodies• deficit of isotype switch
Cellular, combined• severe combined (SCID)
• cytokine signalization• T-cell receptor signalization• recombination of T-cell receptor genes• purine metabolism• expression of HLA molelules
• combined• intercelluar signalization• intracellular signalization • cellular motility• chemokine signalization• transcription factors• IFN gamma/IL-12 pathway
Phagocyte number of phagocytes adhesion function (intracellur killiing)
Complement particular components regulatory factors
Malfunction of regulation cytotoxicity negative feedback apoptosis
Syndromes with compromised DNA repair
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Levels of antibodies in kids production of Ab associated
with cellur development of immune-competent cells (starts during 1st months in utero)
active transport through placenta
IgM
IgG
IgA
delivery 6 months
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IgGIgAIgE
Fischer, Nature Immunology 2004
HSC
TNKCLP
MLP Pro B Pre B
Plasma cells
Mature B
L5 V preB
m
Bone marrow
IgM
IgD
B cell development
Memory B cells
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IgGIgAIgE
Fischer, Nature Immunology 2004
HSC
TNKCLP
MLP Pro B Pre B
Plasma cellsAR agamaglobulinaemiam, Igalfa, Lamda5, BLNK, LRRC8
Mature B
L5 V preB
m
Bone marrow
IgM
IgD
Agammaglobulinaemia - AR
Memory B cells
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IgGIgAIgE
Fischer, Nature Immunology 2004
HSC
TNKCLP
MLP Pro B Pre B
Plasma cellsXLABTK
Mature B
L5 V preB
m
Bone marrow
IgM
IgD
Agamaglobulinaemia - XL
Memory B cells
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Bruton agamaglobulinaemia (XLA) X-linked agammaglobulinemia single gene defect lack of B cells
X
autosomal recessive agammaglobulinaemias (20%)
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VAŠEK, 3 y-o boy
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VAŠEK Personal history IVF, twin A, brother healthy perinatal history unremarkable pneumonia 3 wks before diagnosis regulary vaccinated admitted for laryngitis, septic state
followed
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absence of all immunoglobulins absence of B cells in periphery and bone marrow
VAŠEK Laboratory investigation
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VAŠEK Diagnosis and treatment mutation in a gene coding for Bruton
tyrosinkinase (BTK) regular IVIg substitution currently without clinical symptoms prognosis relatively favourable (danger - echoviruses)
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IgGIgAIgE
Fischer, Nature Immunology 2004
HSC
TNKCLP
MLP Pro B Pre B
Plasma cells
CVIDICOSTACIBAFF-RCD19
Mature B
L5 V preB
m
Bone marrow
IgM
IgD
Hypogammaglobulinaemia
Memory B cells
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Common variable immunodeficiency (CVID) Male /female > 2 years Poor responses to vaccines Serum IgG and IgA are > 2 SD below
mean for age Exclude other 2nd antibody deficiencies
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Common variable immunodeficiency (CVID)
highly heterogeneous manifestation later in life incidence 1 : 10.000 – 50.000 infections, autoimmunity, granulomas ICOS (on T cells) TACI, BAFF-R, CD19 (on B cells)
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IgGIgAIgE
Fischer, Nature Immunology 2004
HSC
TNKCLP
MLP Pro B Pre B
Plasma cells
HIGM
CD40LCD40
AID UNGMature B
L5 V preB
m
Bone marrow
IgM
IgD
Defects of isotype switch
Memory B cells
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Defects in hyper IgM
Notarangelo, J Allergy Clin Immunol 2006, 117, 855-64
X
X
XXX
X
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Hyper IgM syndrom (HIGM) bacterial and atypical infection (PCP, cryptosporidia) defect in communication (previously B cell defect
expected) mainly boys (CD40L = X-linked)
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ONDŘEJ, 8 month-old
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ONDŘEJ Personal history family history unremarkable BCG vaccination in 3 months enlarged left axillar lymphnodes
suppuration drainage consolidation in 4 months cough chronically slurry yellow-green stool since 2 months failure to thrive
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ONDŘEJ Disease detection in 8 months oral thrush
at GP: afebrile, failure to thrive, thrush, tachypnoe, clear breathing
in hospital: at admission sat. O2 80%, leukocytosis, trombocytosis, low ESR, low CRP
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ONDŘEJ Immunological investigation
IgG 0,6 g/l [NR 3.6-7.7]IgA < 0.06 g/l [NR 0.1-0.6]IgE < 1 IU/ml [NR 0-30.0]IgM 1,98 g/l [NR 0.3-1.4]
lymphocyte numberfunctional tests
• (proliferation) • (phacytosis, NBT)
normal
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Hyper IgM syndrome?
IgG, A, E + IgM
and atypical infection
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ONDŘEJ Before transplantationCD3+CD4+CD154+
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mutation in exon 5, Cys800Thy(dr. Genevieve de Saint Basil, Neckar, Pařris)
Notarangelo, J Allergy Clin Immunol 2006, 117, 855-64
Xq26
ONDŘEJ Molecular genetics
mother is CARRIER
ONDŘEJ
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ONDŘEJ After bone marrow transplantation
CD3+CD4+CD154+
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Classification of primary immunodeficiencies
Antibody• agammaglobulinaemia• hypogammaglobulineamia• deficit of specific antibodies• deficit of isotype switch
Cellular, combined• severe combined (SCID)
• cytokine signalization• T-cell receptor signalization• recombination of T-cell receptor genes• purine metabolism• expression of HLA molelules
• combined• intercelluar signalization• intracellular signalization • cellular motility• chemokine signalization• transcription factors• IFN gamma/IL-12 pathway
Phagocyte number of phagocytes adhesion function (intracellur killiing)
Complement particular components regulatory factors
Malfunction of regulation cytotoxicity negative feedback apoptosis
Syndromes with compromised DNA repair
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Cellular and combined PID• severe combined (SCID)
• cytokine signalization• T-cell receptor signalization• recombination of T-cell receptor genes• purine metabolism• expression of HLA molelules
• combined• intercelluar signalization• intracellular signalization • cellular motility• chemokine signalization• transcription factors• IFN gamma/IL-12 pathway
common gamma chain.ZAP-70 RAG1/2, ArtemisADA, PNPHLA I, II
DiGeorge syndrome
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Severe combined immunodeficiecy (SCID)
clinical symptoms• early in life• chronic diarrhea, failure to thrive • graft versus host disease (on skin)
complications after vaccination with live vaccines
unusual infections, severe course family history
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Laboratory findings
lymphopenia• T-B-NK- • T+B-NK+• T-B+NK+
defect in T-cell activation• e.g. n vitro PHA
low serum immunoglobulins• beware – antibody
transferred from mother
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SCID
T-
B+
B-
NK-
NK+
NK-
NK+
c/JAK3 SCID
IL-7R deficiency
RAG1/2 deficiency/ArtemisADA SCID
ADA SCID
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X-SCID
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MICHAL, 5 month-old boy
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MICHAL Personal and family history
o in maternal family a few early deaths of boyso properly vaccinatedo thrived wello exanthema in 4 monthso admitted due to pneumonia
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MICHAL Lab results
IgG 0IgA 0IgM 0.14CD3+: 0.1%CD3-16+/56+: 4.0%CD19+: 96%
T-B+NK-
X-SCIDmutation in common gamma chain gene was found
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MICHAL Exanthema = BCGitis!
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DiGeorge syndrom - CATCH 22
ccardiac defectsaabnormal faciestthymic hypo/aplasiaccleft palatehhypocalcemiadeletion 2222q11
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Classification of primary immunodeficiencies
Antibody• agammaglobulinaemia• hypogammaglobulineamia• deficit of specific antibodies• deficit of isotype switch
Cellular, combined• severe combined (SCID)
• cytokine signalization• T-cell receptor signalization• recombination of T-cell receptor genes• purine metabolism• expression of HLA molelules
• combined• intercelluar signalization• intracellular signalization • cellular motility• chemokine signalization• transcription factors• IFN gamma/IL-12 pathway
Phagocyte number of phagocytes adhesion function (intracellur killiing)
Complement particular components regulatory factors
Malfunction of regulation cytotoxicity negative feedback apoptosis
Syndromes with compromised DNA repair
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Defect of Phagocytosisnumber of phagocytes neutropenia (severe, cyclic)adhesion leukocyte adhesion defect (LAD)function (intracellur killiing) chronic granulomatosis (CGD)
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Leukocyte Adhesion Defect I o subunit of superficial intergrino rolling is impairedo persisiing leukocytosiso delayed umbilical separationo periodontitidiso recurrent skin, respiratory and gut infectionso skin ulcers and necrosiso first transplanted patient with PID in the
Czech Republic (1994)
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Defect of PhagocytosisChronic Granulomatous Disease inability of phagocytes to generete reactive oxygen
radicals gene defect of one or more components of NADPH
oxidase X - linked
• defect in genefor gp91-phox - • membrane bound part of the molecule of cytochrom b558
autosomal recesive defect in genes of membrane or cytoplasmatic subunits p47-phox, p67-phox, p22-phox
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rac
67
47
cytoplasma
elastasecathepsin
primary granules
bacteria
phagosome
fungi
9122
Holland, 2007
CGD
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rac
67 47
cytoplasma
9122
bacteria
phagosome
elastasecathepsin
fungi
Holland, 2007
CGD
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cytoplasma
NADPH
NADP+
9122rac67
47
bacteria
phagosomeelastasecathepsin
fungi
e-O2
HOClH2O2
SOD
MPO
Holland, 2007
CGD
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9122rac67
47
bacteria
phagosome
cytoplasma
elastasecathepsin fungi
NADPH
NADP+
e-O2
HOClH2O2
SOD
MPO
K+
Holland, 2007
CGD
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9122rac67
47
bacteria
phagosome
cytoplasma
elastasecathepsin fungi
NADPH
NADP+
e-O2
HOClH2O2
SOD
MPO
K+XX
Holland, 2007
CGD
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1 phenotype – 4 genotypesX-CGD CYBB, gp91phox (X910, X91-, X91+) 65%
AR-CGD CYBA, p22phox, chr. 16 <5% NCF1, p47phox, chr. 7 25% NCF2, p67phox, chr. 1 <5%
• milder course
incidence 1/100-200.000
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Lymphadenitis
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Granulomas leading to obstruction
Holland, 2007
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Enterocolitis, Crohn-like
Arimura, 2006
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Classification of primary immunodeficiencies
Antibody• agammaglobulinaemia• hypogammaglobulineamia• deficit of specific antibodies• deficit of isotype switch
Cellular, combined• severe combined (SCID)
• cytokine signalization• T-cell receptor signalization• recombination of T-cell receptor genes• purine metabolism• expression of HLA molelules
• combined• intercelluar signalization• intracellular signalization • cellular motility• chemokine signalization• transcription factors• IFN gamma/IL-12 pathway
Phagocyte number of phagocytes adhesion function (intracellur killiing)
Complement particular components regulatory factors
Malfunction of regulation cytotoxicity negative feedback apoptosis
Syndromes with compromised DNA repair
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o deficit of early components of complement cascadeo deficit of late components of complement cascade o deficit in alternative pathway
o hereditary angioedema (deficit C1 inhibitor deficit)
Complement deficiencies
http://www.siamhealth.net/Health/Photo_teaching/urticaria.htm
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Classification of primary immunodeficiencies
Antibody• agammaglobulinaemia• hypogammaglobulineamia• deficit of specific antibodies• deficit of isotype switch
Cellular, combined• severe combined (SCID)
• cytokine signalization• T-cell receptor signalization• recombination of T-cell receptor genes• purine metabolism• expression of HLA molelules
• combined• intercelluar signalization• intracellular signalization • cellular motility• chemokine signalization• transcription factors• IFN gamma/IL-12 pathway
Phagocyte number of phagocytes adhesion function (intracellur killiing)
Complement particular components regulatory factors
Malfunction of regulation cytotoxicity negative feedback apoptosis
Syndromes with compromised DNA repair
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Familial hemophagocytic lymphohistiocytosis (FHL)
o first symptoms in previously healthy baby after infection (mainly EBV)
o low cytotoxicityo highly activated CD8+ T-cellso activation of macrophages leading to
phagocytosis of BM cells
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Prenatal Diagnostics history, affected family member PID with known molecular defect
XLA some forms of SCID chronic granulomatosis
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Investigation of patient with suspected PID history clinical examination laboratory investigation
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Clinical presentation Ask yourself
• Severe• Persistent• Unusual• Recurrent
Be guided by pathogens Beware of surprises !
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Lab tests to reveal PID
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Differential diagnosis of PIDHUMORAL CELLULAR
COMBINEDPHAGOCYTE COMPLEMENT
Frequency 70% 20% 9% 1%
Age <6 m 0 ... < 2 y 0 ... < 2 y all
Symptoms respiratory inf.otitidespneumoniasarthritides
severe respiratory inf.pneumoniasdermatitisdiarrhoea
omphalitisadenitispyodermiaotitides
autoimmunitySLEpyogenic inf.oedema
Infections extracellular b.echoviruses
virusesfungimycobacteria
staphylococcifungienterobacteria
neisseria
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Differential diagnosis of PIDHUMORAL CELLULAR
COMBINEDPHAGOCYTE COMPLEMENT
Complications cardiovascularechoviral inf.
infectionstumorsautoimmunity
infections various
Survival adulthood early childhood individual individual
Diseases XLACVIDsIGAD
SCID CGDLAD
HAE
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General approach in diagnosis of PID
Bonilla, 2005
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Diagnosis of humoral PID
Bonilla, 2005
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Diagnosis of cellular PID
Bonilla, 2005
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Diagnosis of phagocyte PID
Bonilla, 2005
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Diagnosis of complement PID
Bonilla, 2005
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Therapy of PID G-CSF a GM-CSF
neutropenia
gene therapy ADA deficiencyX -linked SCID(LAD, chronic granulomatosis.)
other forms of therapy
IVIG antibiotic and antimycotic
therapy• chronic granulomatosis• LAD
bone marrow transplantation• SCID• LAD • Wiskott-Aldrich syndrome
Interferon gamma• chronic granulomatosis
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Resources
Slatter et al., Clin Exp Immunol, 2008, pp. 389-96 deVries et al., Clin Exp Immnol, 2006, pp. 204-14 Notarangelo et al., J Aller Clin Immunol, 2005, pp 883-96 Bonilla et al., Practice parameters for the diagnosis and management of
primary immunodeficiecy, Annals of Asthma, Allergy and Immunology, 2005, S1-S65
Ochs et al., Primary immunodeficiency Diseases, 2nd edition, Oxford, 2006
ales.janda at lfmotol.cuni.cz