Understanding B and T Lymphocytes in Immune Response

Introduction to Lymphocytes

  • Presented by: Dr. Dona Wijayasinghe

  • Special Thanks: Associate Professor Guna Karupiah

ILO 1: Describe how B and T lymphocytes recognise antigens

Recap: What are antigens?
  • Antigens: Substances that induce an immune response.

  • Antibody: A protein produced by B cells that binds to a specific antigen.

  • Pathogen: A microorganism that can cause disease.

B Cell Recognition of Antigens

B Cell Receptors (BCR)

  • Function: Recognise specific antigens on pathogens.

  • Mechanism:
      - Pathogen antigens are attached to the B cell receptor (BCR).
      - Interaction leads to activation of B cells.

T Cell Recognition of Antigens

T Cell Receptors (TCR)

  • Structure: Different receptors for CD4 Helper T cells and CD8 Cytotoxic T cells.

  • Mechanism of Recognition:
      - Pathogen antigens are processed and presented by Antigen Presenting Cells (APCs).
      - For CD4 Helper T Cells:
        - Processed antigen presented on MHC Class II molecules from APCs (e.g., B cells).
      - For CD8 Cytotoxic T Cells:
        - Processed antigen presented on MHC Class I molecules from infected host cells.

  • Markers:
      - CD4 for Helper T Cells.
      - CD8 for Cytotoxic T Cells.

Self-Recognition by T Cells

How do T Cells Recognise Self-Cells?

  • T cells distinguish between infected cells and normal body cells using MHC markers:
      - MHC Class I for CD8 Cytotoxic T Cells.
      - MHC Class II for CD4 Helper T Cells.

ILO 2: Clonal Selection and Random Generation of Receptors

How are BCRs and TCRs generated?
  • Both B and T cell receptors are specific to pathogens and created before encountering them.

  • Process:
      - Somatic Recombination:
        - Different genes are shuffled to create diverse receptors.
      - Production:
        - Millions of unique receptors are created for both B and T cells.
        - CD4 Helper T Cells and CD8 Cytotoxic T Cells undergo similar processes.

Clonal Selection and Expansion
  • Entry of Pathogen:
      - Pathogen's antigen binds to the specific receptor on B or T cells.
      - Activation occurs leading to:

  • Clonal Selection:
      - The B cell or T cell with the matching receptor is activated.

  • Clonal Expansion:
      - Proliferation of activated cells:
        - B Cells: Form memory B cells and plasma B cells.
        - CD4 Helper T Cells: Form memory T cells.
        - CD8 Cytotoxic T Cells: Form memory T cells.

ILO 3: B Lymphocytes Recognising and Tagging Pathogens for Destruction

Mechanism of B Lymphocyte Action
  • Pathogen Encounter:
      - Recognition involves direct binding of the pathogen to BCRs.

  • Stimulated B Cell: Initiates the immune response.

  • Processes:
      - Clonal expansion enhances the immune response against the specific pathogen.
      - Differentiation into effector cells facilitates targeted destruction of pathogens.

ILO 4: CD4 Helper T Lymphocytes and MHC-II Responses

CD4 Helper T Cell Responses
  • Respond to antigens presented by MHC Class II molecules from APCs.

  • Pathogen Presentation:
      - Pathogen processed and displayed on the B cell or APC's surface.

  • Activated CD4 Helper T Cell:
      - Undergoes clonal expansion to increase the immune response capacity.
      - Plays a crucial role in assisting B cells and cytotoxic T cells in pathogen elimination.

ILO 5: CD8 Cytotoxic T Lymphocytes and MHC-I Responses

CD8 Cytotoxic T Cell Responses
  • Respond to MHC Class I molecules on infected cells.

  • Activation Process:
      - Pathogen-infected cell presents processed antigen on MHC Class I.
      - CD8 T cells recognize this and become activated.

  • Clonal Expansion:
      - Increases the number of cytotoxic T cells available to eliminate infected cells.

  • Memory T Cells:
      - Some cells differentiate into memory T cells for long-lasting immunity.