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Summary Immunological Biotechnology | KU Leuven | 2025/26

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Summary of Immunological Biotechnology (G0P77a) from the Schakeljaar Biochemie en Biotechnologie program at KU Leuven. Covers fundamental immunology concepts including innate immunity, adaptive immunity (B and T cells), MHC functions, antibody structure, T cell-mediated immunity, and humoral immune responses. Ideal for exam preparation and understanding the core mechanisms of immunological systems taught in this bridge year course.

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SUMMARY: IMMUNOLOGICAL
BIOTECHNOLOGY
G0P77a




2025-2026
SCHAKELJAAR: BIOCHEMIE EN BIOTEHNOLOGIE

,Lowie Boels Immunological biotechnology


1. Common causes of disease in humans................................................................................................ 3
2. Phases of the immune response .......................................................................................................... 3
1. Basic concepts of immunobiology .............................................................................................................. 5
1. Cells of the immune system ........................................................................................................... 5
2. The e ector mechanism of immunity ............................................................................................. 9
2. Innate immunity ...................................................................................................................................... 11
3. The early induced immunity...................................................................................................................... 16
4. Adaptive immunity – B cells ...................................................................................................................... 22
1. Structure of B cell receptor and antibody molecule ....................................................................... 22
2. The interaction of an antibody with a specific antigen .................................................................... 23
3. The generation of lymphocyte receptors ............................................................................................ 24
4. Somatic hypermutations and class switching..................................................................................... 26
5. The adaptieve immunity – T cells .............................................................................................................. 29
1. T cell receptor structure ............................................................................................................... 29
2. Co-receptors of the T cell receptor ................................................................................................ 32
3. Antigen presentation to T cells ...................................................................................................... 33
4. The generation of αβ T cell receptor ligands ................................................................................... 33
5. Petide MHCII complexs are generated in acidified endocytic vesicles form proteins obtained by
endocytosis, phagocytosis and autophagy ................................................................................................ 34
6. Intracellular signalling of B and T cells  ITAM’s................................................................................. 36
7. Evolution of the adaptive immune system .......................................................................................... 36
6. MHC and it’s functions ............................................................................................................................. 37
1. The Function of MHC ............................................................................................................................ 37
1. Development of T lymphocytes ..................................................................................................... 40
2. Development of B lymphocytes .................................................................................................... 46
8. T cell mediated immunity ........................................................................................................................ 52
1. The T-Cell Journey: From Naive to E ector ............................................................................................. 52
2. Secondary Lymphoid Organs (SLOs) ..................................................................................................... 52
3. T-Cell Entry into Lymph Nodes .............................................................................................................. 53
4. The Key Players: Antigen-Presenting Cells (APCs) .......................................................................... 54
5. E ector T cells ............................................................................................................................. 58
9. The humoral immune respons ........................................................................................................... 62
1. Overview of Humoral Immune Response ............................................................................................... 62
2. B-cell activation .................................................................................................................................. 62
3. Somatic Hypermutation and A inity Maturation..................................................................................... 66
4. Thymus-Independent Antigens and B Cell Responses ................................................................... 68

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,Lowie Boels Immunological biotechnology
5. Distribution and Functions of Immunoglobulin Classes ......................................................................... 69
10. Integrated dynamics of innate and adaptive immunity ............................................................................. 72
1. Temporal and Spatial Coordination of the Immune Response ................................................................. 72
2. The Concept of Immune Modules ......................................................................................................... 74
3. Integration of Humoral Immunity (Antibodies) .................................................................................... 77
4. Immunological Memory .................................................................................................................... 78
11. The mucosal immune system ................................................................................................................ 80
1. Introduction ..................................................................................................................................... 80
2. The Dual States of Mucosal Immunity.................................................................................................... 80
3. Distinctive Anatomical and Cellular Features ........................................................................................ 81
4. Antigen Handling and Immune Cell Navigation...................................................................................... 81
5. Mechanisms of Active Tolerance and Homeostasis ....................................................................... 83
12. Failures of the immune response ............................................................................................................ 84
1. Introduction to Primary Immunodeficiencies (PID)............................................................................. 84
2. Human Immunodeficiency Syndromes ............................................................................................. 84
3. Newborn Immunity ........................................................................................................................... 85
4. Defects in Activation and Signaling ................................................................................................... 85
5. Autoinflammatory Diseases .............................................................................................................. 86
6. Pathogen Evasion Strategies .............................................................................................................. 87
7. Viruses ............................................................................................................................................. 88
8. Allergies (Hypersensitivity) ................................................................................................................ 89
9. Autoimmunity ................................................................................................................................... 91
10. Pregnancy .................................................................................................................................... 93
13. Manipulation of the immune response .................................................................................................... 94
1. Introduction to Immune Manipulation .................................................................................................. 94
2. Vaccination.................................................................................................................................. 94
3. Using the Immune Response to Fight Tumors ................................................................................ 95
4. Treatment of Unwanted Immune Responses (Autoimmunity) ......................................................... 97




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, Lowie Boels Immunological biotechnology
1. Common causes of disease in humans




2. Phases of the immune response
 The innate immune response is an immediate response and happens in minutes but can last days
 The adaptive immunie respons involves T-cells, B cells and antibodies
 Example:
o A pathogen enther your body and is recognized which induces inflammation due to the innate
immune response
o The adaptive immune response is later on activated  due to the specificity in B and T cells
antibodies are produced against the antigen that was presented by macrophages to the T and B
cells
o Once this pathogen is recognized and antibodies are produced the immune response for next
time will be faster and stronger




3

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