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This set of vocabulary flashcards covers the stages of the adaptive immune response, T-cell differentiation (Th1, Th2, Th17, Treg), the specific mechanisms of the type 2 immune response against helminths involving ILC2s, Tuft cells, and eosinophils, and the associated pathologies.
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Phase 1 of Adaptive Immune Response
Antigen recognition, involving the capture and presentation of antigens by dendritic cells.
Langerhans cell
An immature dendritic cell located in the epidermis that captures antigens and migrates to the lymph nodes to become a mature dendritic cell.
Signal 1 in T cell activation
The interaction between the Peptide-MHC complex on a dendritic cell and the TCR on a T cell.
Signal 2 in T cell activation
The co-stimulatory interaction between CD80/86 on the dendritic cell and CD28 on the T cell.
Signal 3 in T cell activation
The secretion of cytokines, such as IL−12 for Th1 differentiation, that influences T cell polarization.
Th1 subset
A T helper subset characterized by the master transcription factor Tbet, producing IFN−γ and IL−2 for cell-mediated immunity against intracellular pathogens.
Th2 subset
A T helper subset characterized by the master transcription factor Gata−3, producing IL−4, IL−5, and IL−13 for humoral immunity against helminths.
Th17 subset
A T helper subset characterized by the master transcription factor RORγt, producing IL−17A and IL−22 in response to extracellular bacteria and fungi.
Treg subset
Regulatory T cells characterized by the master transcription factor FoxP3, producing IL−10 and TGF−β for immune suppression and mucosal homeostasis.
Alternative macrophage activation
Activation of macrophages by IL−4 and IL−13 secreted by Th2 cells, primarily involved in tissue repair.
Major Basic Protein (MBP)
A toxic protein released by activated eosinophils to mediate the killing of helminths.
Eosinophil Cationic Protein (ECP)
A protein release by eosinophils via FcR-mediated activation to help destroy helminthic parasites.
Tuft cell
A specialized epithelial cell in the small intestine that identifies helminths (via succinate and SUCNR1) and produces IL−25 to activate ILC2s.
ILC2 (Group 2 Innate Lymphoid Cells)
Innate lymphoid cells that respond to IL−25, IL−33, and TSLP to produce IL−5 and IL−13 for helminth defense and allergic inflammation.
Goblet cell hyperplasia
An increase in mucus-producing goblet cells in the intestinal epithelium, induced by IL−13 during a helminth infection.
Basophils in helminth response
Cells that produce IL−4 and respond to IL−33 and TSLP to support the differentiation of Th2 cells and B cell IgE production.
M cells
Specialized cells in the Gut-Associated Lymphoid Tissue (GALT) that deliver bacteria and antigens from the intestinal lumen to dendritic cells and Peyer's patches.
Granulomatous Reaction
A chronic inflammatory response, such as that seen in Schistosoma mansoni infection, which can lead to severe fibrosis and cirrhosis.
Epileptogenesis in Helminth Infection
The development of epilepsy as a pathology of neurocysticercosis, caused by inflammation, calcification, and perilesional edema.
Carcinogenesis associated with Helminths
The development of cancers such as cholangiocarcinoma (bile duct cancer), bladder cancer, or hepatocarcinoma due to helminthic infection.