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76 Cards in this Set
- Front
- Back
Complement Receptor Type I
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Found on phagocytes, neutrophils, B cells, Eosinophils, RBC
Serve to phagocytize and clear immune complexes cleaves c3b and c4b as a regulatory control - make sure their isnt over production of complement |
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Complement Receptor Type II
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Found on B cells, Dendritic Cells
B cells - helps to activate dendritic cells - helps to trap antigens in the germinal center Serves as a receptor for EBV -HIJACKER |
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Complement Receptor Type III
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Found on Mononuclear phagocytes, neutrophils, and NK Cells
Serves to phagocytize Helps the WBC adhere to the endothelium via ICAM |
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Complement Receptor Type IV
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Found on mononuclear phagocytes, neutrophils, and NK Cells
Serves to phagocytize Helps the WBC adhere to the endothelium |
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Purpose of Complement (3)
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1. to opsonize the macrophage for phagocytosis (c3b or c4b)
2. stimulate immune response (c3a and c5a) 3. cell lysis via mac - c3b 4. B Cell Activation - C3d (cleavage product of C3b) binds to C receptors on B cells; initiates immune responses |
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Complement Deficiencies of the Classical Pathway
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C2 & C4 - autoimmune dieases (SLE)
C3 - leads to gram + bacterial infections |
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Complement Deficiencies of the Alternative Pathway
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Properdin & Factor D - leads to gram + bacterial infections
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Complement Deficiencies of the MAC
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CD5-9 leads to Neisseria bacterial infections
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Receptors on T helper lymphocytes, T cytotoxic cells, B lymphocytes, and NK Cells
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T helper cells: CD 3+. CD 4+
T cytolytic cells: CD 3+, CD 8+ B lymphocytes: Fc Receptors; Class II MHC, CD 19 & CD 21 NK Cells: Fc receptor for IgG |
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Name all 5 Immunoglobulins and their subclasses
What are elevated Ig indicative of? |
IgG - gamma 1-5
IgM - none IgA - alpha 1 and alpha 2 IgE - none IgD -ANy Ig elevations are indicative of cancer |
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IgG
IgG3 |
- principal mediator of secondary immunity
- can cross the placenta and provide passive protection to the fetus IgG3 - most effective at binding complement bc it has a large hinge region, however the large hinge is susceptible to proteases |
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Elevated IgG levels are indicative of:
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infections, liver diseases, autoimmune diseases, cystic fibrosis, sarcoidisis
severe: myeloma, monoclonal gammopathy |
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IgM
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-prinicipal mediator of primary immune response
- pentamer with s-s bond to a j chain - increases antigen agglutination visibility |
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Elevated IgM levels are indicative of:
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IgM monoclonal gammopathy, infection,PARASITIC INFECTION, liver diseases, autoimmune diseases, nephrotic syndrome, polycythemia vera, HEROIN ADDICTION, Waldenstrom's macroglubulinemia
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IgA1 & IgA2
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IgA1 - monomer present in the circulation
IgA2 - dimer is the predominant antibody in mucosal secretions |
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Elevated IgA levels are indicative of:
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IgA monoclonal gammopathy, infections, liver diseases, cystic fibrosis, CELIACS, Berger's disease, sarcoidosis,
memory jog: A = Angel Hair Pasta can't be eaten in Celiacs |
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IgD
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rare; found on surface of B cells
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IgE
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-binds to very high affinity Fc receptor on mast cells & basophils, lymphocytes
- mediator of hypersensitivity, allergies, asthma - primary antiparasitic antibody, sensitizes worms and other parasites for destruction by eosinophils - sends signals to mast cells saying "fire" |
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Elevated IgE levels are indicative of:
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allergic disorders, hypersensitivity disorders, parasitic infections, immunologic disorders, infectious mononucleosis, IgE myeloma
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Toll like receptors
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-found on phagocytes
TLR 1, 2, 4, 5 9 - bacteria sensitive - TLR 2 - bacterial comp - TLR 4 - for LPS - TLR 9 - for bacterial and viral DNA sequences TLR 3, 7, 8 are viral sensitive and found on the endosome - not the plasma membrane - TLR 3 - recognizes ds RNA |
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Chromosome location of heavy chain gene
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chromosome 14
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Chromosome location of light chain kappa
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chromosome 2
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chromosome location of light chain gamma
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chromosome 22
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Origin of Acute Lymphocitic Leukemia
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Pro B Cell
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Origin of Chronic Lymphocytic Leukemia
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Mature B Cell with overexpression of kappa or lambda light chains
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Origin of Myeloma
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Mature Plasma Cell leading to Bence Jones Proteinuria - light chains in the urine
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Burkitt's Lymphoma
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translocation of chromosomes 14 and 8 . So the heavy chains on chromosome 14 are affected.
C-myc gene is placed in front of the heavy chain promoter which leads to gross overproduction of heavy chains |
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Isotype Switching Methods
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1. IL - 4 induces IgE isotype switching
2. TGF - B increases IgA production 3. IFN- Gamma enhances IgG2a |
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An increased sedimentation rate for erythrocytes is associated with:
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Induction of fibrinogen by IL-6
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Which neurotransmitter associated with the induction of fever?
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Prostaglandin E
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Role of IL 1/ TNF
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Leukocyte migration to site of injury
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Role of EGF
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epithelial and fibroblast growth
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Role of TGF Beta
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inhibits the division of the cell
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Role of TGF alpha
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promotes the division of the cell
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Immunodeficiency Disease Types
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- B & T Cell Maturation deficits
- B & T cell activation deficits - signaling deficits - multi - system deficiencies -phagocyte disorders - complement system deficiencies |
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SCIDS - signs
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-failure to thrive
- candidiasis - chronic diarrhea |
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SCIDS - causes
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-IL 2 gamma receptor deficits - 2, 7, 9, and 4 - especially 7
-JAK -ADA - adenosine deaminase - RAG 1/RAG2 deficits - so no TCR or Ig |
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DiGeorge's Syndrome - signs
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-Deficient T cells - so susceptible to intracellular microbes and viruses
-absent parathyroids = Tetany due to Ca2+ deposits - facial deformities - |
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X-Linked agammaglobulinemia - causes
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-B Cell tyrosine kinase gene deficiency leading to lack of maturation past Pre-B stage
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Di Georges - Causes
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failure of development of the third and the fourth pouch
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X linked Agammaglobulinemia - signs
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-reduced plasma cells
- no germinal centers - normal t cells - autoimmune diseases |
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Bare lymphocyte Syndrome - types and differences
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-MHC Class II deficit - affects both MHC I and MHC II
- MHC Class I deficit - TAP deficiency and shows up as NK Cells and gamma-delta T cells |
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Bare Lymphocyte Syndrome - symptoms
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-Frequent URIs
- chronic lung infections -skin lesions |
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Signaling Defects
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-Zap 70 defects
-CD3 error - X-Linked Hyper IgM |
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Ataxia Telangiectasia - cause
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mutation @ ATM gene on chromosome 11 leading to neurologic deficits and hematopoietic cancer
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Wiskott ALdrich Syndrome
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No platelets leads to Eczema .
- due to mutation in WAS protein - results in low IgM levels hint: Baby with Ezcema |
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Chronic Grabulomatous Disease
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deficit in cytochrome b558 results in inability to produce peroxide
- results in inflammatory reactions and non malignant granulomas hint: Michael Jackson nose |
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Leukocyte Adhesion Deficiency - LAD 1
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deficiency of CD 18 Beta 2 on WBC prevents it from migrating to inflammatory site
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Leukocyte Adhesion Deficiency - LAD2
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No fucose - so Leukocyte can not interact with E and P selectins
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Heriditary Angioneurotic Edema
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failure of C1 inhibitor to stop complement cascade resulting in edema
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Location of B cells in the Lymph node and spleen
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B cells are found primarily in the marginal zone of the spleen and in the follicles of the lymph nodes
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Location of T helper & T cytolytic cells in the Lymph nodes and spleen
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T helper cells localize in the periarteriolar lymphoid sheath (PALS) in the spleen ad the paracortex of lymph nodes.
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Purpose of Pcam
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diapedesis of WBC
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Purpose of Il 1 and TNF alpha
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stimulation of inflammatory response
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LFA Icam
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involved in wbc adhesion
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Positive Selection
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Process by which T cells which express a low avidity to MHC are selected to survive
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Negative Selection
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process by which T cells which express a high avidity to MHC are eliminated
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Medullary areas of the Lymph node are inhabited by:
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activated T cells and plasma B cells
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Where are idiotypic determinants found on on Antibodies
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In the variable region
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What does TdT regulate?
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Increased diversity in both the TCR and Ig molecules.
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What cells are capable of antigen presentation?
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B cells, macrophages, activated T cells and others
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what bonds are responsible for the formation of antibody/antigen interactions?
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All non covalent bonds
1. hydrogen bonds, 2. electrostatic interactions, 3. Van Der Waals interactions [induced dipoles], 4. hydrophobic interactions [exclusion of water]). |
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true or false: Before Th Cells differentiate into Th1 and Th2 they are doubly positive
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false: T helper cells are not shown to be doubly positive at any point
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How are Th1 cells stimulated from Th Cells? What do they produce?
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-Th 1 cells are stimulated by IL 12 and make :
-IFN gamma which is involved in macrophage activation and isotype switching - LT and TNF activate and recruit WBC to the site of inflammation * think : CMI responses to viruses/intracellular pathogens. |
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How are Th 2 cells stimulated from Th Cells and what do they produce?
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-Th2 cells are stimulated by IL-4 and make :
-IL 4 - stimulates IgE production -IL - 5 - stimulates Eosinophil recruitment - IL 10 which inhibits the activation of macrophages |
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What can happen if you mount the wrong Th (1 v 2) response to a bacterial infection?
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If a person is infected w/ M. Leprae, two responses can occur:
-Th1 = tuberculoid leprosy - Th2 = Lepramatous Leprosy --> FAR HIGHER BACTERIAL COUNT!! |
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During development, which of the following is the first protein product synthesized by a B cell?
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Mu heavy chain
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define epitope and paratope
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-epitope - part of antigen that binds directly to the antigen
- paratope - region of the antibody that binds directly to the antigen |
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what components of CTL are important for killing?
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Perforin and granzyme B stored in granules
-also contains IFN gamma, but it is not stored in granules |
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What cells are associated with a granulomatous reaction?
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epithelioid macrophage
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What is the characteristic inflammatory cell associated with an allergic response?
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Eosinophil
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A patient with severe asthma gets no relief from antihistamines. The symptoms are MOST likely caused by:
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Leukotrienes
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Where is IgD most often seen?
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IgD is primarily seen on the surface of B cells and is used as a marker of B cell development
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Poison Ivy
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A T cell response to a specific antigen
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Where in the Antibody does somatic hypermutation occur?
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Occurs in the hypervariable region
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What immunoglobulins to peripheral or circulating immunoglobulins express?
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IgM and IgD, after undergoing rearrangement of heavy and light chain genes
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