A) It is a member of the Src family of kinases.
B) It binds to the cytoplasmic tails of T cell coreceptors CD4 or CD8.
C) It phosphorylates ITAM motifs on the CD3 complex.
D) It phosphorylates tyrosine residues on Zap-70 and activates it.
E) It phosphorylates PIP2 to PIP3 and leads to the activation of Itk.
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Multiple Choice
A) NF-B
B) Jun
C) Fos
D) NFAT
E) Ras
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Multiple Choice
A) Activated T cells receive survival signals from antigen during an infection.
B) Activated T cells contribute to the activation of antigen-presenting cells via CD40 ligand.
C) Memory T cells generated during a primary immune response express high levels of interleukin-2 receptors and actively proliferate long after the primary response is completed.
D) The major effector function of helper T cells is to activate macrophages and other cells by releasing cytokines.
E) When an infection is eliminated,activated T cells die by apoptosis.
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Multiple Choice
A) Pleckstrin homology (PH) domain
B) Proline-rich (PR) domain
C) SH1 domain
D) SH2 domain
E) SH3 domain
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Multiple Choice
A) Btk
B) Itk
C) Tec
D) PI-3 kinase
E) Zap-70
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Multiple Choice
A) Binding of peptide-MHC complexes on the APC to the TCR on the T cell
B) Binding of CD4 on the T cell to nonpolymorphic regions of class II MHC molecules on the APC
C) Binding of integrins on the T cell with adhesion ligands on the APC
D) Binding of B7-2 on the APC with CD28 on the T cell
E) Binding of CD40L on the T cell with CD40 on the APC
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Multiple Choice
A) The therapeutic peptides,called "altered peptide ligands," could inactivate T cells specific for myelin proteins,or drive them to differentiate into T cells that do not produce IFN-
B) The therapeutic peptides,called "altered peptide ligands," could interfere with processing of the natural myelin proteins by the patient's antigen-presenting cells.
C) The therapeutic peptides could bind to the TCRs of myelin-specific T cells but not to the self MHC molecules,thereby blocking T cell activation.
D) The therapeutic peptides could down-regulate MHC expression.
E) The therapeutic peptides could replace the damaged myelin and restore neuronal function.
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Multiple Choice
A) Formation of the immunologic synapse
B) Recruitment of signaling molecules,such as LAT,to glycolipid-enriched domains known as lipid rafts
C) Enhanced adhesion between T cells and antigen-presenting cells (APCs) via T cell integrin LFA-1 and its ligand on the APC,ICAM-1,at the central zone of the immunologic synapse
D) Clustering of the TCR and coreceptors leading to phosphorylation of ITAMs on CD3 by Lck
E) Binding of CD28 with costimulators on APCs in the cSMAC,resulting in signal transduction activation
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Multiple Choice
A) CD40-dependent isotype switching is required to produce antibody isotypes that activate T cells.
B) CD40 ligand is required for CTL killing of CD40-expressing infected cells.
C) CD40 ligand is required for maturation of CD4+ T cells in the thymus.
D) CD40 ligand on activated T cells binds to CD40 on antigen-presenting cells (APCs) ,and this enhances the expression of B7-1,B7-2,and cytokines by the APCs.
E) CD40 ligand on T cells binds to B7-1 and B7-2 on APCs,and this enhances the function of the APCs.
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Multiple Choice
A) B7-1 and B7-2 expression on antigen-presenting cells (APCs) is upregulated by the presence of "danger" signals,such as lipopolysaccharide,as well as cytokines,such as interferon (IFN) -
B) B7-1 and B7-2 are expressed at low levels on some resting APCs.
C) Induction of B7-1 usually occurs before the induction of B7-2 in an immune response.
D) B7-1 and B7-2 bind to CD28 on T cells and provide "second signals" for naive T cell activation.
E) Activated helper T cells can induce expression of B7-1 and B7-2 on APCs via CD40L binding to CD40.
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Multiple Choice
A) Expression of its gene requires multiple transcription factors,such as Fos,Jun,and NFAT.
B) It acts as an autocrine growth factor for T cells.
C) It binds to CD25 on the cell membrane of T cells.
D) It is only involved in the proliferation of helper T cells and not CTLs.
E) It promotes susceptibility of T cells to apoptosis.
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Multiple Choice
A) TCR ? Lck ? Zap-70 ? LAT ? Grb-2 ? SOS ? Ras ? Erk ? Fos
B) TCR ? Lck ? Zap-70 ? LAT ? SOS ? Grb-2 ? Ras ? Erk ? Fos
C) TCR ? Lck ? ITK ? LAT ? Grb-2 ? SOS ? Ras ? Erk ? Fos
D) TCR ? Lck ? Zap-70 ? LAT ? SOS ? Grb-2 ? Ras ? Erk ? Jun
E) TCR ? Lck ? Zap-70 ? LAT ? PLC ? DAG ? calcium release
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Multiple Choice
A) Kupffer cells
B) B cells
C) Follicular dendritic cells
D) Neutrophils
E) Langerhans cells
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Multiple Choice
A) Zap-70
B) RAG-1
C) CD3
D) Pre-T
E) TCR
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Multiple Choice
A) Antigen receptors on T cells bind to MHC molecules for only brief periods of time.
B) The affinity of most TCRs for peptide-MHC complexes is similar to the affinity of antibodies for their antigens.
C) Only 1% or less of the MHC molecules on any antigen-presenting cell (APC) display a peptide recognized by a particular T cell.
D) T cells usually require multiple engagements with an APC before a threshold of activation is reacheD.
E) A subthreshold number of MHC-TCR interactions can lead to T cell inactivation.
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