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		<swivt:creationDate rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2026-07-31T11:51:56+00:00</swivt:creationDate>
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		<rdf:type rdf:resource="https://www.wikidoc.org/index.php/Special:URIResolver/Category-3APages_using_duplicate_arguments_in_template_calls"/>
		<rdfs:label>WBR0681</rdfs:label>
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		<property:AnswerA rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Defect in B-cell maturation</property:AnswerA>
		<property:AnswerAExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Common variable immunodeficiency (CVID) is due to a defect in B-cell maturation.</property:AnswerAExp>
		<property:AnswerB rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Inability of T cells to reorganize actin cytoskeleton</property:AnswerB>
		<property:AnswerBExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Wiskott-Aldrich syndrome is characterized by the inability of T cells to reorganize actin cytoskeleton.</property:AnswerBExp>
		<property:AnswerC rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Failure of Th1 cells to produce IFN-gamma</property:AnswerC>
		<property:AnswerCExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Hyper-IgE syndrome is characterized by the failure of Th1 cells to produce IFN-gamma.</property:AnswerCExp>
		<property:AnswerD rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Defect of the BTK gene</property:AnswerD>
		<property:AnswerDExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">X-linked (Bruton's) agammaglobulinemia is characterized by a defective BTK gene.</property:AnswerDExp>
		<property:AnswerE rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Defective CD40L on helper T cells</property:AnswerE>
		<property:AnswerEExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Hyper-IgM syndrome is characterized by defective CD40L on helper T cells</property:AnswerEExp>
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		<property:Explanation rdf:datatype="http://www.w3.org/2001/XMLSchema#string">The patient has elevated levels of IgM, which is a pentamer that is produced in the immediate response against pathogens. The shape of IgM is important to allow it to maximally trap antigens. Given the patient's elevated IgM, and deficiency of all other Ig classes, he most likely suffers from hyper IgM syndrome. Hyper IgM syndrome (type 1)is an X-linked disorder caused by a defective CD40L on helper T cells. CD40L (L for Ligand) binds to CD40 on antigen presenting cells, and it's deficiency or mutation prevents immunoglobulin class switching, leading to a deficiency in all classes of immunoglobulin except IgM the primary immunoglobulin produced by B-cells during an antigen response. Four other types of hyper IgM syndrome have bee characterized, all with different modes of inheritance and different mutations involving any of the receptors involved in immunoglobulin class switching. Patients with hyper IgM syndrome classically present with recurrent pyogenic infections (among which Pneumocystis jirovecii pneumonia is very common) due to the inability to mount an appropriate immune response, particularly with the lack of secretory IgA.&lt;br/&gt;
'''Educational Objective:''' IgM is a pentamer. It is increased in hyper IgM syndrome, that is commonly caused by  a defective CD40L on helper T cells.&lt;br/&gt;
'''References:''' Image attribution: Artur Jan Fijałkowski&lt;br&gt;
Etzioni A, Ochs HD. The hyper IgM syndrome--an evolving story. Pediatr Res. 2004;56(4):519-25.&lt;br&gt;
First Aid 2015 page 205</property:Explanation>
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		<property:RightAnswer rdf:datatype="http://www.w3.org/2001/XMLSchema#string">E</property:RightAnswer>
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		<property:WBRKeyword rdf:resource="&wiki;Antibody"/>
		<property:WBRKeyword rdf:resource="&wiki;Infection"/>
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		<swivt:wikiPageModificationDate rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2020-10-28T01:23:53Z</swivt:wikiPageModificationDate>
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