primary immunodeficiency disorders (pid) soheila alyasin m.d. associat professor of pediatrics...
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Primary Immunodeficiency Disorders (PID)
Soheila Alyasin M.D. AssOCIAT Professor of Pediatrics Division of Immunology and Allergy
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Definition
The immunodeficiency disorders are a diverse group of illnesses that, as a result of one or more abnormalities of the immune system, increase susceptibility to infection.
The PID are not associated with other illnesses that impair the immune system.
Many are genetic disorders with a characteristic inheritance pattern.
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Incidence
Estimated occurrence of PID is 1 per 10000 live birth, excluding the asymptomatic Ig A def
First IRPID report: CVID was the most common PID in Iran
Since 1952 more than 150 different PID disorders had been defined
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Problems in Early Diagnosis of PID
Early diagnosis needs high index of suspicion
No screening is available in the perinatal period or later in childhood
Wide spread use of antibiotics for respiratory infections mask the course of disease
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Indications for evaluation of a child for PID
one or more systemic or serious bacterial infections (sepsis, meningitis)
TWO or more serious respiratory or documented bacterial soft tissue infections (cellulitis, ABCESS, pneumonia, draining otitis media, or lymphadenitis ), within one year
Infections occurring at unusual sites (liver or brain abscess)
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Indications for evaluation of a child for PID, Cont..
Infections with unusual pathogens (Aspergillus, Serratia marcescens, Nocardia or Burkholderia cepacia,pneumocystis jiroveci)
Severe unusual infections with common childhood pathogens
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Initial evaluation of immune system
History Ab,C & neutrophil:encapculated
bacteria Nl G/D unless bronchiectasis T :oppurtunistic infections ,FTT Physical exam Family history
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Relative distribution of the primary immunodeficiency Antibody deficiencies 65% Combined cellular and antibody
deficiencies 15% Phagocytic deficiencies 10% Cellular deficiencies 5% Complement deficiencies 5%
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Initial Immunology Testing of Patients With Recurrent
InfectionsCBC+manual differential count ESR
ANC, ALC, Howell-Jolly bodies, platelet countScreening test for B cell defects :IgA, IgG, IgM measurementIsohemagglutininsAntibody titers to Tetanus, Diphteria, H.influenza, and
S.Pneumonia
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Initial Immunology Testing of Patients With Recurrent
Infections
CBC+manual differential count ESR
ANC,(Nl: LAD & neutropenia unlikely) ALC,(Nl: unlikely T cell defect) Howell-Jolly bodies,( exclude asplenia) platelet count(Nl exclude WAS)
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Initial Immunology Testing of Patients With Recurrent
Infections
Screening test for B cell defects :IgA, IgG, IgM measurementIsohemagglutininsAntibody titers to Tetanus, Diphteria,
H.influenza, and S.Pneumonia
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Initial Lab testing, cont..
Screening tests for phagocytic cell defects:
Absolute neutrophil countRespiratory burst assay (NBT, RDT)
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Initial Lab testing, cont..
Screening tests for T cell defects:
Absolute lymphocyte count (Nl: unlikelyTcell defect) Candida albicans intradermal test
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Initial Lab testing, cont,..
Screening test for complement deficiency:
CH50
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Primary Defects of Antibody Production
Recurrent infections with encapsulated bacteria
Repeated respiratory infections since 6-9 months of life
The most common PID Selective IgA deficiency:1/333
persons to 1/16000, XLA 1/50000
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X-Linked Agammaglobulinemia
(XLA or Bruton Agamma) Profound defect in B lymphocyte
development Severe hypogammaglobulinemia Absence of circulating B cells Small to absent tonsils No palpable lymph node Xq22 encode the B-cell protein Tyrosine
Kinase (Btk) which is responsible for pre-B-cell expansion and maturation
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Genetic Diagnosis of XLA
Low or undetectable Btk mRNA and kinase activity in all patients ( >250 mutations)
Carrier: Non random X-chromosome inactivation in B-cells or by direct mutation analysis
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Clinical Manifestations of XLA
Maternally transmitted IgG antibodies protect the patient for the first 6-9 mo
Frequent respiratory infections with extra cellular pyogenic organisms:
Strep pneumonia, H.influenza,Mycoplasma,
Not frequent viral and opportunistic infections (except for p.c.,enterovirus ,echovirus, hepatitis viruses)
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Phenotypic Diagnosis of XLA
Lymphoid hypoplasia Decreased IgG, IgA, IgM and IgE
far below 95% confidence limit, usually less than 100 mg/dl of total immunoglobulin
Abnormal titer of isohemagglutinins and post vaccination antibody titer
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Phenotyping Diagnosis of XLA, Cont..
Flow cytometry: The absence of circulating B cells (vs. CVID)
Normal Tcell count and function
TREATMENT : IVIG ,Abx
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Common Variable Immunodeficiency (CVID)
Hypogammaglobulinemia with phenotypically normal B cells
The same kind of infections and organisms as XLA
Later onset of infections, and less severe infections,male=female,no echo virus
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Genetic of CVID
No identified molecular diagnosis A shared hereditary influence with
selective IgA deficiency ( MHC class III over the chromosome 6)
Drugs( phenytoin, D pencillamine, gold ,sulfasalazin)
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Phenotypic characteristics of CVID
Normal B cell number but no response to pokeweed mitogen in vitro
T cell number is normal but T cell function is depressed in some patients
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Clinical manifestation of CVID
Low serum immunoglobulin Auto antibody GI and autoimmune
manifestations,CVD(tymoma,A. areata,hemolytic anemia)
Nodular follicular lymphoid hyperplasia Normal or enlarged size of LN Splenomegaly (25%)
Malignancy in older age(lymphoma 400 fold)
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Selective IgA deficiency
Isolated absence of serum and secretory IgA Serum IgA <10 mg/dl
The most common well defined PID 0.33% in healthy blood donors Basic genetic defect is still unknown B cells are normal Autosomal dominant inheritance with
variable expressivity Commonly occurs in pedigree with CVID
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Selective IgA Def, Clinical Manifestations
Mostly asymptomatic Infections occur predominantly in
the respiratory, gastrointestinal, and urogenital tracts
Polio vaccination induce the local IgM and IgG production
IgG2 subclass def is reported
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Selective IgA Def, Clinical manifestation, cont..
Auto antibody & autoimmune dis Malignancy Anti IgA antibodies (44%)IVIG infusion is not indicated
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Transient Hypogamm of Infancy (THI)
The nadir amount of IgG is reached at 3-4 months of life
Extension of the physiologic hypogamm beyond 6 months of age so called: THI
Normal T and B cell number and normal T cell function
Normal titer of isohemagglutinins and post vaccination antibody response
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THI
Increased frequency of otitis media and sinusitis, not life threatening infection
IVIG therapy is not indicated
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Hyper IgM syndrome
Heterogeneous genetic basis Low serum IgG and IgA Normal or elevated IgM Mutations in two genes on the X
chromosome: CD154 (CD40 ligand) and NEMO and two genes on the autosomal chromosomes; AID and CD40
Bacterial infections, Opportunistic infections, and Malignancy
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X Linked lymphoproliferative
disease (XLP) Duncan disease Defective gene: Xq25 led to
absence of a regulatory molecule (SH2D1A)
Uncontrolled cytotoxic T-cell immune response to EBV
Antibody def is frequently present
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Clinical Manifestation of XLP
Previously healthy male Three major clinical phenotypes:Fulminant infectious mononucleosis
(50%)Lymphomas, B cell lineage (25%)Acquired hypogamm (25%)
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Treatment of B cell ID
The only effective treatment:Judicious use of antibioticsRegular replacement therapy with
IVIG Except for CD40 ligand defect and
XLP:B.M. transplantation
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IVIG Therapy
IVIG has a broad spectrum of antibodies from pool of plasma of more than 60000 donors
Safe and effective but expensive needed to give monthly(3-4 wks):
400-600mg/kg iv infusion Systemic reactions can occur but raretrue anaphylaxis due to anti IgA antibody
(IgE)
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