diagnosis and management of immunodeficiency in adulthood teresa tarrant, md assistant professor of...
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![Page 1: Diagnosis and Management of Immunodeficiency in Adulthood Teresa Tarrant, MD Assistant Professor of Medicine Division of Rheumatology, Allergy, and Immunology](https://reader035.vdocuments.net/reader035/viewer/2022062301/56649d7f5503460f94a6297d/html5/thumbnails/1.jpg)
Diagnosis and Management of Immunodeficiency in Adulthood
Teresa Tarrant, MD
Assistant Professor of Medicine
Division of Rheumatology, Allergy, and Immunology
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The Immune System:
http://stemcells.nih.gov/info/scireport/chapter6.asp
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Pattern of infections: Clinical Immunology
T cell deficiencies Fungi Viruses Pneumocystis
B-cell deficiencies S. pneumococcus H.influenzae Enteroviruses
Complement deficiencies Bacteremia Meningitis C5-9: Neisseria C1/2/4: SLE
Phagocytic disorders Staph skin infections Cepacia Infections of the
reticuloendothelial system Abscesses
The type of infectious agent and the location of the infection may give valuable insight into the nature of the immunologic defect. . .
Humoral Immunodeficiencies
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Clinical Scenario: Recurrent infections 32 yo previously
healthy female who has a 3 year history of sinus drainage and recurrent sinus infections. . .
Differential: Allergies Chronic sinusitis Allergic fungal sinusitis Antibiotic resistance Mechanical
derangement
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Clinical Scenario:Recurrent infections 32 yo previously
healthy female who has a 3 year history of sinus drainage, recurrent sinus infections, who developed bilateral otitis media requiring tympanostomy and IV antibiotics. . . .
Differential Allergies Chronic sinusitis Allergic fungal sinusitis Antibiotic resistance Mechanical derangement Humoral immune
deficiency CF Primary Ciliary Dyskinesia
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Clinical Scenario:Recurrent infections
Now it’s the same 32 yo female . . . who develops fevers, increased sputum, and an infiltrate seen on CXR
DifferentialHumoral immune
deficiencyCFPrimary Ciliary
Dyskinesia
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Differential for Humoral Immune Deficiency in Adults Drugs
Antimalarials, captopril, carbamazepine, steroids, gold, penicillamine, phenytoin, sulfasalazine
Systemic disorders Chronic medical
conditions CF Sickle Cell
Hypercatabolism of Ig Excessive loss of Ig
Nephrosis, burns, diarrhea, lymphangiectasia
ID HIV, EBV
Malignancy CLL Immunodeficiency with
thymoma (Good’s syndrome)
NHL CVID IgA deficiency IgG Subclass
deficiency
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Common Variable Immunodeficiency
Definition: a disease characterized by low levels of immunoglobulins and recurrent sinopulmonary infections.
It is a relatively common immunodeficiency with variable levels of immunoglobulins and clinical course between patients
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CVID
Heterogeneous group of disorders of humoral immunodeficiency with associated bacterial infections, autoimmune disease, and malignancy
Bimodal distribution Major peak 25-45 yo Second peak 5-15 yo
M=F Prevalence estimated at 1:25,000-50,000
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CVID: Pathogenesis
Some molecular defects identified TACI mutation (~20% of CVID)
Most cases are sporadic Familial inheritance has been
demonstrated□ X-linked□ Autosomal recessive□ Autosomal dominant
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CVID: Genetic Mutations in the genes encoding the tumor
necrosis factor (TNF) superfamily receptorsTACI mutation
Transmembrane activator and calcium-modulating ligand interactor
BAFF-R mutation B cell activation factor of the TNF family receptor
Small number of patients with CD19 deficiency
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TACI mutation TACI is expressed on
the surface of B cells TACI interacts with
BAFF (activation factor) APRIL (proliferation
ligand)
TACI-deficient mice show ↑ B cells, impaired isotype switching and develop autoimmune manifestations with (SLE)-like symptoms, lymphoproliferation,splenomegaly, and lymphoma
Bacchelli et al. Clin Exp Immunol 2007; 149:1365-2249
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CVID: Pathogenesis
Familial inheritance IgA deficiency
Kindreds with IgA deficiency and CVID 15% of patients with CVID have a first degree
relative with IgA deficiency Individuals with IgA deficiency who develop
CVID
MHC haplotypes shown to correlate with CVID and IgA deficiency
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CVID: Pathogenesis
Environmental triggersViral infectionDrugs
Antimalarials, captopril, carbamazepine, steroids, gold, penicillamine, phenytoin, sulfasalazine
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CVID: Clinical Manifestations
Infectious DiseaseRecurrent pyogenic sinopulmonary infectionsChronic enteroviral infectionsMeningoencephalitisChronic Giardia LambliaRecurrent HSV and/or VZV
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CVID: Clinical Manifestations
GI manifestationsSprue-like syndrome (wt loss, diarrhea, vitamin
deficiency, hypoalbuminemia)Nodular follicular hyperplasia of the
intestinesGastric atrophy, achlorydriaColitisMALT lymphomaGiardiasis
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Nodular Lymphoid Hyperplasia of the Duodenum
Nodules develop through lymphocyte proliferation in the lamina propria and submucosa, but are not directly linked to increased malignant potential.
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CVID: Clinical Manifestations Autoimmune manifestations (22-50%)
Pernicious anemia Vitiligo Autoimmune thrombocytopenia Autoimmune hemolytic anemia Autoimmune thyroiditis Alopecia areata Keratoconjunctivitis sicca Inflammatory Arthritis
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CVID: Clinical Manifestations
Hematologic manifestationsGranulomatous disease
Noncaseating epithelioid granulomas of liver, lung, spleen, skin, gut
AmyloidosisTonsilar tissue normal or enlargedLymphadenopathy25% splenomegaly
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CVID: Clinical Manifestations
Malignancy300+ fold increase in lymphomas in women
between 50-60 yo50 fold increase in gastric carcinomaThymomaMALT lymphomaLymphoreticular malignancy
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CVID: Clinical Manifestations
Pulmonary manifestationsPneumoniaAsthmaBronchiectasisLymphoid interstitial pneumonia (LIP)Pulmonary Fibrosis
Best predictor of improved pulmonary outcome is early diagnosis and aggressive treatment.
J. de Gracia, et al., Int Immunopharmacol 4 (2004), 745–753.
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Laboratory evaluation of Humoral Immune Deficiency
Targetted H&P for recurrent infections and autoimmunity
Quantitative serum Ig (age and sex matched controls)
Measurement of Ab production Pneumococcal polysaccharide HIB polysaccharide Tetnus toxoid
Measurement of quantitative Ag-specific Ig titer pre- and post-immunization 4 week post-immunization level within protective range and
>4 fold rise from baseline Peripheral blood lymphocyte subset analysis
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Quality not Quantity
Measurement of Antigen-specific (i.e. tetanus, HIB, pneumococcal) IgG titer pre- and post-immunization4 week post-immunization level within
protective range and/or >4 fold rise from baseline
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Immunoglobulin Defects
<2 SD below the mean in IgG and another Ig class or <5th percentile of total IgG for a given age
Poor or absent response to immunization<Two-fold increase in Ag-specific titer
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CVID: Clinical Surveillance
PFT’s High resolution CT of the chest to evaluate
for bronchiectasis Stool O&P, bacterial cx, C. difficile for
changes in GI sx CBC q6 mo for autoimmune cytopenias Low threshold for lymphoma
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Treatment of CVID IVIG
Higher doses to keep trough IgG levels >500 mg/dl decreases infections, hospitalizations, need for abx therapy and improves pulmonary function
0.2-0.6 g/kg/mo or 300-500 mg/kg/q2-4 weeks IV IV and subcutaneous routes equally effective Pre-existing chronic lung disease is not improved by IVIG
Stiehm, E et al. Pediatr Infect Dis J, 1997. 16 (7): 696-707.
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IVIG First licensed in 1981 for primary antibody
deficiencies as an improved, less painful alternative to IM injections of IG
Subtle differences in Ab titers, IgA depletion, and IgG subclass that vary between lots as well as manufacturers Gammagard-SD, Polygam-SD: IgA def patients
Preparations with high titer specific IG against infectious pathogens Cytogam: High titered IVIG for CMV Respigam: High titered IVIG for RSV
Increased toxicity with live virus vaccines (MMR) Do not administer within 3 months of vaccination
T ½ 15-30 days
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Side Effects of IVIG Mild side effects occur in approximately 10% of infusions Side effects often preventable with ASA (15 mg/kg/dose) or
acetominophen (15 mg/kg/dose) with diphenhydramine (1mg/kg/dose).
Occasionally, hydrocortisone (6mg/kg/dose, max=100mg) 1hr prior
Stiehm, E et al. Pediatr Infect Dis J, 1997. 16 (7): 696-707.
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Infectious Disease Transmission with IVIG
Hepatitis C has been reported after administration of certain lots of IVIG Cases appeared after Hep C Ab+ patients were
excluded as donors Hypothesis is that Hep C Ab neutralizes virus in
donor pools Consequently new pasteurization +/-
solvent/detergent processing and testing for HCV RNA to reduce viral transmission
Several IVIG lots were recalled after donors developed Creutzfeldt-Jakob disease No cases were reported of CJD transmission
No cases have been reported of HIV transmission
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Subcutaneous IgG (Vivaglobulin)
Ochs HD et al; Subcutaneous IgG Study Group. Safety and efficacy of self-administered subcutaneous immunoglobulin in patients with primary immunodeficiency diseases.J Clin Immunol. 2006 May;26(3):265-73.
Moller G et al: Subcutaneous immunoglobulin replacement in patients with primary antibody deficiencies: safety and costs. Lancet. 1995 Feb 11;345(8946):365-9.
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Selective IgA deficiency
Severe deficiency or total absence of the IgA class of immunoglobulins
Estimated prevalence 1:500-1:1000 persons
Spectrum of clinically affectedAsymptomaticRecurrent infections: sinopulmonary, diarrhea
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Selective IgA deficiency
Higher incidence of autoimmunityRASLE ITP
AtopyAsthmaFood allergy
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Selective IgA Deficiency
TreatmentSupportive
Risk of anaphylaxis to blood productsFormation of IgG or IgE anti-IgA antibodies
Subset with IgG2 subclass deficiency
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IgG Subclass Deficiency
The IgG class of antibodies is composed of four different subtypes of IgG molecules IgG1, IgG2, IgG3, and IgG4
Patients who lack, or have very low levels of, one or two IgG subclasses, but whose other immunoglobulin levels are normal, are said to have a selective IgG subclass deficiency.
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IgG Subclass Deficiency The clinical significance of abnormal IgG subclass
levels in patients with recurrent infections is unclear A low level of at least 1 IgG subclass has been found
in approximately 2% of a given population, and Impaired antibody production may not be seen among adult patients with IgG3 subclass deficiency
A low level of 1 or more IgG subclasses alone is generally not considered sufficient for a diagnosis of immunodeficiency
In individuals with recurrent infections and 1 or more low levels of IgG subclasses, a demonstrable impairment in antibody response to vaccination or natural exposure is considered the most important determinant of disease
Bonilla F et al, Ann Allergy Asthma Immunol. 2005 May;94(5 Suppl 1):S1-63.
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Putting it all together. . .
H&P: Pattern of recurrent infections
Rule out secondary causes of immune dysfunction Medications Other chronic diseases Protein wasting states
Laboratory assessment: quality not quantity. Measurement of antigen-specific Ig titers pre- and
post-immunization
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Primary Humoral Immunodeficiency
Referral to a Clinical Immunologist IVIG or SQ Ig only where there is
demonstrable impairment in IgG production of antigen-specific antibody titers (quality not quantity)
Supportive antibiotics Vaccinations: Prevnar, HIB, influenza Surveillance for associated clinical
conditions
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Key References
Immune Deficiency Foundation website: http://www.primaryimmune.org/
Orange JS et al. Use of intravenous immunoglobulin in human disease: a review of evidence by members of the Primary Immunodeficiency Committee of the American Academy of Allergy, Asthma and Immunology. J Allergy Clin Immunol. 2006 Apr;117(4 Suppl):S525-53.
Bonilla F et al. Practice parameter for the diagnosis and management of primary immunodeficiency. Ann Allergy Asthma Immunol. 2005 May;94(5 Suppl 1):S1-63.
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Additional References Conley, ME et al. Diagnostic criteria for primary immunodeficiencies.
Clin Immunol 1999. 93 (3): 190-7. Stiehm, E et al. Human intravenous immunoglobulin in primary and
secondary antibody deficiencies. Pediatr Infect Dis J, 1997. 16 (7): 696-707.
Spickett, GP et al. Common variable immunodeficiency: how many diseases? Immunol Today, 1997. 18 (7): 325-8.
Rosen, FS et al. Medical progress: the primary immunodeficiencies. NEJM 1995. 333 (7): 431-40.
Spickett, GP. Current persepctives on common variable immunodeficiency (CVID). Clin & Exper Immunol 2001. 31 (4): 536-42.
Middleton, E (ed) et al. Allergy Principles and Practice. 5th Ed. Mosby 1998. 724-5.
Ballow, M. Primary immunodeficiency disorders: antibody deficiency. Curr Rev Allergy and Clin Immunol 2002. 109 (4): 581-91.
Bacchelli et al. Clin Exp Immunol 2007; 149:1365-2249.
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Additional References Cunningham-Rundles, C et al. Common variable immunodeficiency: clinical
and immunological features of 248 patients. Clin Immunol 1999. 92: 34-48. Sweinberg SK et al. Retrospective analysis of the incidence of pulmonary
disease in hypogammaglobulinemia. J Allergy and Clin Immunol 1991. 88 (1) 96-104.
Buckley, RH et al. The use of intravenous immne globulin in immunodeficiency diseases. NEJM 1991. 325 (2): 110-116.
Punnonen, J et al. IL-4 synergizes with IL-10 and anti-CD40 MoAbs to induce B-cell differentiation in patients with common variable immunodeficiency. Scand J Immunol 1997. 45: 203-12.
Farrington, M et al. CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency. PNAS 1994. 91: 1099-1103.
Schaffer, FM et al. Individuals with IgA deficiency and common variable immunodeficiency shar polymorphisms of major histocompatibility complex class III genes. PNAS 1989. 86: 8015-9.
Massimo, M et al. Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency. Blood 2001. 98 (5): 1321-5.