MHH, Seminarroom 15.02.2010 14.30h. Antigen + Basophils + CD4 + T cells  T H 2 cells IL-4 Fc  RI MHC II.

Slides:



Advertisements
Similar presentations
Chapter15 B cell mediated immune response. B cells mediated immune response Humoral immunity(HI) or antibody mediated immunity: The total immunological.
Advertisements

Lectures 1 & 2 The immune system Overview
Models for in vivo and in vitro studies on basophils
Understanding the Immune System
Humoral Immunity.
Acquired Immunity Defends Against Infection of Body Cells and Fluids By: Jonah Harrington, Josh Yi.
Pathogen invasion MM Neutrophil DC PRR Naïve T cell CTL IFN-  B cell IgG IL-4, IL-5, IL-6 Th1 Th2 IgE IgA Cell lysis Tr cell IL-1 , TNF- , chemokines.
Transplantation MCB150 Beatty
Microbiology 204: Cellular and Molecular Immunology Class meets MWF 11-12:30 Lectures are open to auditors Discussions are restricted to those enrolled.
Anusara Daenthanasanmak Autophagy is the process involving the degradation of a cell's own components through the lysosomal machinery.
General Microbiology (Micr300)
Principles of Immunology Cells of the Immune System 1/26/06 “Those who have health, have hope. Those who have hope have everything.” Arabian proverb.
Immune Cells , Receptors, and Markers. Lymphoid Tissues and Organs.
Cells of inflammation and Immunity G. Wharfe 2005.
Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Chapter 14 Specific Immunity (adaptive immunity)
Dental Microbiology #211 IMMUNOLOGY Lecture 5 Cellular Immunity: The functions of T cells.
Bellwork Discuss with your group what you think is happening in the following processes. Why does your body undergo an allergic reaction? Why do some.
GILT Accelerates Autoimmunity to the Melanoma Antigen Tyrosinase-Related Protein 1 The Journal of Immunology, ,08,31 Xu Zhenjie.
12 Immune Response to Biomaterials CHAPTER
Lecture #10 Aims Describe T cell maturation and be able to differentiate naïve and effector T cells. Differentiate the development and functions of Th1.
Antigen Presentation/Cell cooperation in Antibody response Pin Ling ( 凌 斌 ), Ph.D. ext 5632; References: 1. Male D., J. Brostoff,
Antibodies.
IMMUNOLOGY By ZOHA and SAMIHA.
Dr Shoaib Raza.   B lymphocytes are also called as B-Cells  Develop in the yolk sac  Migrate to bone marrow  Processing, differentiation and maturation.
Inducing and expanding regulatory T cell populations by foreign antigen Karsten Kretschmer NATURE IMMUNOLOGY 2005; 6:1219.
MHC Molecules Our immune system has the remarkable ability, and responsibility, of responding appropriately to a wide variety of potential pathogens in.
NAJRAN UNIVERSITY College of Medicine NAJRAN UNIVERSITY College of Medicine Microbiology &Immunology Course Lecture No. 15 Microbiology &Immunology Course.
Basic Immunology University of Tabuk Faculty of Applied Medical Science Department of Medical Laboratory Technology Mr.AYMAN.S.YOUSIF MSc.Medical Microbiology.
Immune system Haixu Tang School of Informatics. Human lymphoid organs.
ORGANIZATION OF THE IMMUNE SYSTEM different cell types diffuse communication network between cells ‚signal transduction’ and inhibition similarity to the.
Lecture 7 Immunology Cells of adaptive immunity
Lecture overview Objective: To understand the mechanisms by which naïve T cells are specifically activated, and the resulting phenotypes of antigen.
Summary J.Ochotná.
Volume 42, Issue 3, Pages (March 2015)
Heat shock protein vaccination and directed IL-2 therapy amplify tumor immunity rapidly following bone marrow transplantation in mice by Robert G. Newman,
Odelya E. Pagovich, MD, Bo Wang, MD, Maria J
Virus-specific IgE enhances airway responsiveness on reinfection with respiratory syncytial virus in newborn mice  Azzeddine Dakhama, PhD, Young-Mok Lee,
CD28 provides T-cell costimulation and enhances PI3K activity at the immune synapse independently of its capacity to interact with the p85/p110 heterodimer.
by Éric Aubin, Réal Lemieux, and Renée Bazin
Immune Tolerance to Self-Major Histocompatability Complex Class II Antigens after Bone Marrow Transplantation: Role of Regulatory T Cells  Allan D. Hess,
Odelya E. Pagovich, MD, Bo Wang, MD, Maria J
Volume 30, Issue 4, Pages (April 2009)
Volume 18, Issue 5, Pages (May 2003)
Volume 6, Issue 4, Pages (April 1997)
by Sanne M. Meinderts, Per-Arne Oldenborg, Boukje M. Beuger, Thomas R
Volume 10, Issue 9, Pages (March 2015)
Tilo Biedermann, Martin Röcken, José M. Carballido 
Adam C. Silver, Alvaro Arjona, Wendy E. Walker, Erol Fikrig  Immunity 
Volume 44, Issue 1, Pages (January 2016)
Volume 39, Issue 4, Pages (October 2013)
Role of B cells in TH cell responses in a mouse model of asthma
Volume 29, Issue 6, Pages (December 2008)
STAT1−/− APCs favor type 17 immune polarization.
Th1 and Th2 immune responses
CD40, but Not CD40L, Is Required for the Optimal Priming of T Cells and Control of Aerosol M. tuberculosis Infection  Vanja Lazarevic, Amy J Myers, Charles.
CTLA-4 Regulates Induction of Anergy In Vivo
Volume 31, Issue 4, Pages (October 2009)
Volume 42, Issue 2, Pages (February 2015)
Volume 15, Issue 11, Pages (June 2016)
Volume 30, Issue 4, Pages (April 2009)
T Cell Activation and proliferation
Volume 38, Issue 2, Pages (February 2013)
Peripheral Tolerance of CD8 T Lymphocytes
APCs from hypertensive mice present antigens more efficiently.
Toll-Dependent Control Mechanisms of CD4 T Cell Activation
Dissecting the Multifactorial Causes of Immunodominance in Class I–Restricted T Cell Responses to Viruses  Weisan Chen, Luis C. Antón, Jack R. Bennink,
Amy Bergtold, Dharmesh D. Desai, Anamika Gavhane, Raphael Clynes 
Epicutaneous Immunization with Autoantigenic Peptides Induces T Suppressor Cells that Prevent Experimental Allergic Encephalomyelitis  Margaret S. Bynoe,
Rapamycin inhibits IL-4—induced dendritic cell maturation in vitro and dendritic cell mobilization and function in vivo by Holger Hackstein, Timucin Taner,
Volume 25, Issue 3, Pages (September 2006)
Presentation transcript:

MHH, Seminarroom h

Antigen + Basophils + CD4 + T cells  T H 2 cells IL-4 Fc  RI MHC II

representing less than 1% of circulating white blood cells susceptible to staining by base dyes Basophils appear in many specific kinds of inflammatory reactions can be found in unusually high numbers at sites of ectoparasite infection (e.g. ticks) basophils are primary effector cells in allergic disorders Basophils

Splenic Basophils in Strongyloides venezuelensis infected mice Higher percentages of Basophils in Strongyloides venezuelensis infected mice Baophils (0.2% naive, 5.84% inf.) Mastcells (0.02%naive, 0.39% inf.) Fc  RI + c-Kit - = Basophils Fc  RI + c-Kit + = Mast cells Strongyloides venezuelensis

Cytokine production of Basophils after Strongyloides infection in vitro Basophils from infected mice produce large amounts of „T H 2 cytokines“ Basophils + IL-3 (24h)

Same amount of MHCII expression on Basophils of naive and infected mice=  MHCII expression is no limiting factor for TH2 induction MHC II expression on Basophils

Ability of basophils to induce naive CD4 + T cells to develop into TH2 cells without IL4

with IL4 Ability of basophils to induce naive CD4 + T cells to develop into TH2 cells

 Basophils from infected mice are able to induce TH2 development without IL4 without IL4 with IL4 Ability of basophils to induce naive CD4 + T cells to develop into TH2 cells

Bone marrow basophils induce T H 2 cells in vitro Expression of MHC II and costimulatory molecules  Bone marrow basophils express MHCII, CD80, CD86

of IL4 -/- mice (G4/G4)Basophils of wt mice Basophils of wt mice are able to induce naive CD4+ cells to develop into TH2 cells Basophils produce sufficient IL-4 for maximum development of TH2 cells Bone marrow basophils induce T H 2 cells in vitro without IL4 with IL4

Basophils pulsed with antigen-IgE complexes are potent APCs Basophils + DNP-OVA + CD4 + T cellsT H 2 cells Basophils are able to process DNP-OVA into OVA(323– 339) and to display peptide fragment in association with MHC class II and to produce IL-4 The enhancing effect of IgE anti-DNP on basophil- induced T H 2 cell development was most apparent when basophils were pulsed with low concentrations of DNP-OVA Basophils + DNP-OVA + IgE anti DNP + CD4 + T cellsT H 2 cells - +

CD4 + T cells + OVA or DNP-OVA +/- IgE anti-DNP  These results suggest that basophils, taking advantage of their expression of Fc  RI, might efficiently take up low doses of antigen in an IgE-dependent way of DNP-OVA Proliferation assay of CD4 + T cells

APC activity of basophils and sorted CD11c + splenic DCs by changing the ratio of APCs to naive CD4 + T cells In presence of IgE-complex even low ratios of basophils induce T H 2 development

in vitroin vivo Basophils are able to induce naive CD4 + cells to develop into TH2 cells in vitro

OVA-pulsed basophils induce T H 2 cells in vivo Basophils + DNP-OVA + IgE anti DNP  mice + challenge with OVA  CD4 + T cells + OVA-pulsed  T–spleen cells Basophils induce T H 2 development in vivo

OVA-pulsed basophils induce T H 2 cells in vivo Basophils + DNP-OVA + IgE anti DNP  mice + challenge with OVA  CD4 + T cells + OVA-pulsed  T–spleen cells Basophils induce T H 2 development in vivo DCs induce T H 1 but not T H 2 development in vivo

OVA-pulsed basophils induce T H 2 cells in vivo Does OVA-pulsed basophils induce IgE and IgG1 production? OVA-pulsed basophils induce IgE and IgG1 production Basophils are important to induce T H 2 responses in vivo Basophils + OVA  mice

Intravenous administration of antigen-IgE complex induces T H 2 responses IC = Immune Complex (DNP-OVA + IgE anti DNP) MAR-1 = anti-Fc  RI  Basophils efficiently take up IC and induce T H 2 development in vivo Depletion of Basophils blocks T H 2 development and therefore IgG1 production of B cells What happens aftre depletion of basophils?

Intravenous administration of antigen-IgE complex induces T H 2 responses Does IL-3 administration increases the number of basophils? Higher numbers of basophils lead to increased production of IgE and IgG1 Yes, it does! Influence on Antibody production?

Summary Basophils produce large amounts of „T H 2 cytokines“ IL-4 and IL-13 after uptake of antigen Basophils are potent APCs Basophils are able to induce naive CD4 + cells to develop into TH2 cells Intravenous administration of antigen-IgE complex induces TH2 responses in vivo Antigen + Basophils + CD4 + T cells  T H 2 cells IL-4 Fc  RI MHC II

Thank you for your attention!