Immunological diagnosis (Institute of Immunology, ZJU)
Immunodiagnosis Detection of Antigen and antibodies Detection of Cellular Immunity
Traditional Immunoassays Anitgen-Ab reaction Agglutination(aggregation) Assays: Immunodiffusion Complement Fixation EIA (IHC/ELISA/ELISPOT) Immunofluorescence (IFA FACS) CLIA (Chemiluminescence immumoassay) Traditional Immunoassays Modern Immunoassays
1. Principles and influencing factors of Ag-Ab reaction 1) Principles of Ag-Ab reaction Specificity reversal combination Concentration and ratio of Ag and Ab
Precipitin curve Immune complex Antibody excess zone
2) influencing factors of Ag-Ab reaction electrolytes Temperature:37 degree pH:pH6-8
2 Methods for detection of Ag or Ab A. Agglutination reaction a. Principle When the particle Ags interact with the appropriate Ab, they clump together and eventually form masses that become large enough to be seen. b. Types direct agglutination reaction indirect agglutination reaction
B. Precipitation reaction a. Principle When soluble Ags come in contact with specific Ab, they precipitate. Precipitation can be demonstrated via immunodiffusion in a semisolid medium (e.g. agar). b. Types immunonephelometry: the formation of IC in solution is monitored by spectrometry. single immunodiffusion double immunodiffusion immunoelectrophoresis
C. Complement fixation test Ag and Ab reactions lead to the formation of IC that activates complement system by classical pathway. This may be exploited to detect the amount of unknown Ag or Ab.
D. Immuno-labeling techniques a. Principle Specific Abs (or Ags ) labelled with fluorescein, enzymes, colloidial gold or radioisotopes are used as probes for the detection of Ags (or Abs). b. Types
Enzyme immunoassay (EIA) EIA is to use enzyme-labeled Abs or Ags to detect Ag and Ab interactions. The enzyme converts a colorless substrate (chromogen) to a colored product. ELISA: Ag or Ab in solution Enzyme immunohistochemistry: Ag in tissue
Enzyme linked immunosorbent assay, ELISA The advantages of ELISA include specificity, sensitivity, rapidity, inexpensiveness, and safety. Enzyme: horseradish peroxidase, HRP Substrates: diaminobenzidine (DAB) 3,3’,5,5’-tetramethylbenzidine (TMB)
6. ELISA to detect Ab (HIV, HCV) to detect Ag
Immunofluorescence Immunofluorescence assay is to use a fluorescent compound (usually fluorescein) to detect the binding of Ag and Ab. The Ab is labeled with the fluorescent compound and its presence is revealed using a fluorescence microscope. Direct, indirect immunofluorescence and indirect complement amplified immunofluorescence
Radioimmunoassay, RIA Chemiluminescence immunoassay, CLIA Immunoblotting, Western blotting Immuno-PCR, IM-PCR Immunologic colloidal gold signature, ICE
Immunoblotting
B G T R A Absorbent material Gold nanoparticle labeled anti-HCG (mouse IgG) Ag(HCG,human chorionic gonadotropin) mouse anti-HCG (immobilized) Anti-mouse IgG (immobilized)
Is there anything wrong ? (first,positive;second,negative) positive negative
2. Detection the Function of Immune cells 1) Isolation of immune cells A Isolation of PBMC: Ficoll Urografin density-gradient separation B: Isolation of lymphocytes and subsets. a,immunoabsorbing assay b. immunomagnetic separation c. FACS d. peptide-MHC tetramer technique
Figure A-23
Figure A-26 MACS:magnetic cell sorting 1,The target cell are labeled with Ab-conjugated magnetic paticles 2,The labeled cells are placed within a magnetic fields. 3, The labeled cells are retained in the magnetic fields while the unlabeled cells are washed away
FACS separation The basic principle of FACS is immunofluorescence and therefore flow cytometers can be considered to be specialized fluorescence microscopes. The modern flow cytometer consists of a light source, collection optics, electronics and a computer to translate signals to data Isolation of different cell populations by FACS relies on the different expression of surface Ags.
Identification of cell subsets by FACS Type of cell CD markers stem cells CD34+,CD31- all leukocyte groups CD45+ Granulocyte CD45+,CD15+ Monocytes CD45+,CD14+ T lymphocyte CD45+,CD3+ T helper cell CD45+,CD3+,CD4+ Cytotoxic T cell CD45+,CD3+,CD8+ B lymphocyte CD45+,CD19+ or CD45+,CD20+ Thrombocytes CD45+,CD61+ Natural killer cell CD16+,CD56+,CD3- B cell T cell CD4+ T cell CD8+ Tcells Tregs (CD4+CD25+) Conventional CD4 Immune Cell types and subtypes defined by surface markers (CDs)
2) Lymphocyte function assays T cell function assay --Proliferation --DTH --Apoptosis --Phagocytosis --Cytokine
T cell proliferation -MTT Mitochondria enzyme catalyze the reduction of MTT – Turn blue
T cell proliferation FACS-CFSE staining
CTL Assay Supernatant
Tetramer Tetramers can bind to three TCRs at once, allowing specific binding in spite of the low (10-6 molar) affinity of the typical class I-peptide-TCR interaction.
DTH Immunization Challenge (Ear/Foogpad) Measurement (Calipers)
Detection of Cytokine production Real-time PCR (mRNA Level) ELISA/ELISPOT Intracellular staining (FACS)
Intracellular Staining Identification of different T helper cells characterized by different cytokine production
Application of Immunoassay Diagnosis of Diseases infectious diseases Immunodeficiency diseases Autoimmune disease hypersensitivity Tumour
Application of Immunoassay Immune surveilence HBV HIV