Clinical Immunology · MU Plovdiv

1. Clinical Immunology. Subject and parts – general characteristics. Basic humoral and cellular mechanisms for the development of defense and immunopathological reactions.

Inside: 5 sections · 4 labelled pictures · 1 table · 25 flashcards · 8 min

Topic 1 of 14 in the MU Plovdiv syllabus for Clinical Immunology (Medicine, Year 4). The free AceMed note covers it in 5 sections, about 1,083 words (8 min of reading), with 25 flashcards.

In this note

  1. Introduction
  2. Immunity as a biological phenomenon
  3. Types of immunity
  4. Immunopathology and hypersensitivity reactions
  5. Hypersensitivity and autoimmune diseases

Introduction

Clinical immunology studies the immune system in health and disease. This topic covers immunity as a biological phenomenon, its types (innate and adaptive, humoral and cellular, active and passive), and the basic humoral and cellular mechanisms behind protective and immunopathological reactions: hypersensitivity (allergy), autoimmunity and immunodeficiency.

Immunity as a biological phenomenon

  • Immunity is the state of an organism having the biological defenses to fight a disease.
  • It is defined as the ability of multicellular organisms to resist harmful microorganisms from entering it.
  • Immunity is a complex biological system.
  • A key function is that the immune system recognises and tolerates self (own body).
  • It involves both specific and non-specific components.

Types of immunity

Natural resistance (innate immunity)

  • Also referred to as the non-specific response; it is quick to respond and present/active from birth.
  • It is the non-specific, immediate response to pathogens. It lacks immunologic memory, is short-lasting, and does not improve upon subsequent exposures.
  • It consists of physical, chemical, molecular, and cellular defences.
  • Major components include skin and mucous membranes, phagocytic leukocytes (neutrophils and macrophages), specialised lymphocytes (NK cells), and several plasma proteins including proteins of the complement system.
  • It can distinguish self from non-self. The response is rapid and prevents the establishment of infection.
  • Specific mechanisms:
  • physical barriers;
  • chemical barriers (lysozymes, pH, lipids, enzymes, complement factors, interferons, acute phase proteins, antimicrobial peptides);
  • normal human flora (microbiota);
  • cellular factors such as phagocytosis, inflammatory response, and fever.

Acquired immunity (adaptive immunity)

  • The immune system that is pathogen specific and not genetically conferred.
  • It is based on antibodies and specifically reactive T lymphocytes, acquired through immune system stimulation by microbial antigens.
  • It develops after a latent period of 1-2 weeks.
  • Immune memory develops, leading to stronger responses in subsequent infections: the secondary response is accelerated and augmented. It provides long-lasting protection.
  • Adaptive immunity has two types: humoral and cell mediated.
  • Humoral immunity is immunity mediated by macromolecules in extracellular fluids (humours), including antibodies and complement proteins. It involves the production of antibodies by plasma cells derived from activated B-cells. It protects the body by neutralizing pathogens, facilitating opsonization, activating complement, and preventing pathogen adherence. Antibodies can only attack viruses outside of their host cells.

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