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Related Concept Videos

Antigens Involved in Adaptive Immunity01:26

Antigens Involved in Adaptive Immunity

An antigen is any substance the immune system identifies as foreign and potentially harmful to the body, prompting an immune response. Antigens have two functional properties: immunogenicity and reactivity. Immunogenicity is the ability of an antigen to stimulate a specific immune response. At the same time, reactivity describes the antigen's ability to react with the cells and antibodies produced in response to it.
Complete Antigens
Complete antigens possess both immunogenicity and reactivity.
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MHC molecules are key players in the immune response, enabling T cells to recognize and respond to specific antigens. They are present on the surface of all nucleated cells in the body and are instrumental in presenting antigens to T cells and activating them. T cells recognize the MHC-antigen complex and initiate an immune response. MHC class I and MHC class II are two main types of MHC molecules, each associated with a distinct antigen processing pathway.
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T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
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Conserved Binding Sites

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Related Experiment Video

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A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
07:59

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes

Published on: March 25, 2014

A probabilistic meta-predictor for the MHC class II binding peptides.

Oleksiy Karpenko1, Lei Huang, Yang Dai

  • 1Department of Bioengineering (MC063), University of Illinois at Chicago, 851 South Morgan Street, Chicago, IL 60607, USA. okarpe2@uic.edu

Immunogenetics
|December 20, 2007
PubMed
Summary

Integrating multiple computational tools enhances major histocompatibility complex (MHC) class II peptide binding predictions. This novel meta-predictor offers improved accuracy over individual methods for diverse MHC alleles.

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Area of Science:

  • Immunoinformatics
  • Computational Biology
  • Peptide-MHC Binding Prediction

Background:

  • Multiple computational methods exist for predicting MHC class II binding peptides, each with limitations.
  • Accurate prediction of MHC class II binding peptides is crucial for vaccine design and immunotherapy.

Purpose of the Study:

  • To develop and evaluate a novel meta-predictor for MHC class II binding peptides by integrating multiple prediction tools.
  • To enhance the reliability and accuracy of peptide-MHC binding predictions through a probabilistic approach.

Main Methods:

  • A probabilistic meta-predictor was constructed to integrate outputs from various individual peptide-MHC prediction tools.
  • The meta-predictor was computationally evaluated using MHC class II peptides from 13 human (HLA) and 3 mouse MHC alleles.
  • Data was sourced from the Immune Epitope Database and Analysis Resource (IEDB).

Main Results:

  • The integrated meta-predictor demonstrated superior performance compared to six state-of-the-art individual predictors.
  • The study confirmed enhanced prediction reliability using a diverse set of MHC alleles and experimentally validated peptides.
  • The developed computational framework is adaptable for MHC class I binding predictions.

Conclusions:

  • The integrative approach significantly improves the reliability of MHC class II binding peptide predictions.
  • This probabilistic meta-predictor offers a flexible and extensible framework for immunoinformatics applications.
  • The methodology can be readily applied to MHC class I binding prediction, broadening its utility.