Immunology Chapter 1

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Last updated 12:20 AM on 9/18/26
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100 Terms

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Innate

Adaptive

Types of immune defenses

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Immunity

State of protection

Specific for disease

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Vaccines

Kick in adaptive defenses to get to immunity

Skips innate defenses

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Antibiotics kill many commensal bacteria —> Pathogenic bacteria take up the space the normal flora previously occupied —> Produce toxins —> Mucosal injury —> RBCs & WBCs leak into the gut between the injured epithelial cells

How can long term antibiotic use lead to further infections (primarily in the gut)

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Opportunistic Pathogen

Pathogen that can become harnful when new conditions arise


ie, c.diff, H. pylori

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Bacteria

Virus

Parasites

Fungi

Types of pathogens

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Protozoans - Eukaryotic

Helminthes - Worms, multicellular

Types of parasites

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Innate Defenses

Immediate barriers & response (ie, skin, mucosal surfaces)

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Skin

Physical barrier

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Sebum

Creates an acidic environment on the skin’s surface

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Mucous

Traps pathogens

Mostly in the upper respiratory tract

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Cilia

Propels pathogens up and out of the body

Mostly in the upper respiratory tract

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Lysozyme

Chemical compound that breaks down bacterial cell walls

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  1. Recognition - Cells (neutrophils)/Soluble components (complement) recognize something foreign

  2. Response - Depends on what recognized the pathogen; Neutralize, kill, inflammation, etc


Innate Immune Response Stages

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Inflammation

The innate immune response causes [?] at site of infection

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Redness (erythema) & Heat (due to vasodilation)

Swelling (edema) (due to increased vascular permeability)

Pain (due to kinins)

S&S of Inflammation

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  1. Pathogen cell surface induces cleavage & activation of complement

  2. One complement fragment (C3b) binds to pathogen; Other (C3a) attracts an effector Cell

  3. Complement receptor on the effector cell binds to C3b on the pathogen

  4. Effector cell engulfs the pathogen, kills it, & breaks it down


General: Pathogen-Recognition by effector cell using complement

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Cytokines

Hormones of the immune system

Soluble proteins that interact with other cells to trigger the innate immune response

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  1. Surface wound introduces pathogen —> Activates effector cells in the area to secrete cytokines

  2. Vasodilation & increased vascular permeability allows fluid, protein, & inflammatory cells to leave the blood and enter the injured tissue

  3. Infected tissue becomes inflamed —> Redness, heat, pain, swelling


Inflammation pathway

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Adaptive immune response

The [?] adds to an ongoing innate immune response

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Adaptive Immune Response

Specific

Adaptable

Memory

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  1. Recognition by T or B cells

  2. Response


Adaptive Immune Response stages

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Rapid (within hours)

Fixed

Limited number of specificities

Constant

Characteristics of the recognition mechanisms of innate immunity

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Slow (days-weeks)

Variable

Numerous highly selective specificities

Improves during response

Characteristics of recognition mechanism of adaptive immunity

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  1. Progenitor cells give rise to a large number of lymphocytes with different specificities DURING DEVELOPMENT

  2. DURING INFECTION, lymphocytes with receptors that recognize the pathogen are activated

  3. Proliferation of pathogen-activated lymphocytes (clonal selection) give effector cells that terminate the infection & produce memory cells to remember the infection


Stages of B/T Cell Response

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Effector Cells

Memory Cells

Cell types made through clonal selection when certain lymphocytes proliferate and differentiate

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Clonal Selection

Proliferation & differentiation of pathogen-specific lymphocytes —> Stimulated by the antigen

Creates Effector Cells & Memory Cells

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Memory Cells

Goal of vaccines

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Hematopoietic stem cells

Immune system cells w/ different functions all derive from [?]

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Common lymphoid precursor

Common myeloid precursor

Hematopoietic stem cell creates…

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Lymphoid lineage

B Cells, T Cells, and Natural Killer cells all come from the [?]

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B-Cell

NK/T-Cell Precursor

Common lymphoid precursor creates…

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T Cell

NK cell

NK/T Cell precursor creates…

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Granulocyte-macrophage progenitor

Megakaryocyte/erthyroid progenitor

Common myeloid precursor creates…

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Myeloid & Erythroid

The Common Myeloid Precursor creates the [?] & [?] cell lineages

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Macrophage & Dendritic cell precursor

Neutrophil

Eosinophil

Basophil

An unknown precursor

Granulocyte-macrophage progenitor creates…

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Mast Cell

The granulocyte-macrophage progenitor creates an unknown precursor which then creates …

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Monocyte

Dendritic Cell

Macrophage & dendritic cell precursor creates…

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Macrophage

Dendritic Cell (maybe)

Monocytes create…

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Megakaryocyte

Erthyroblast

Megakaryocyte/erythroid progenitor creates…

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Platelets

Megakaryocytes create…

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Erythrocyte (RBC)

Erythroblasts create…

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Neutrophils

Most abundant WBC

1st Responders

Short-lived - Last ~3 days

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Kill Pathogens

Produce cytokines to start an inflammatory response

2 Major functons of the Neutrophil

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Eosinophils

Fight parasites

(particularly helminthes

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Mast Cells & Basophils

Primarily responsible for allergies

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Dendritic Cells

Wander around looking for pathogens

Good at starting adaptive immune response

Phagocytosis = primary function

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Monocytes & Macrophage

Killing pathogens through phagocytosis

Produce cytokines

Wander around blood stream (monocytes) & tissues (macrophages) looking for pathogens to kill

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Macrophage

Monocyte that has entered the tissue

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Natural Killer Cell

Type of lymphocyte

Larger than T & B Cells

Natural ability to kill tumor cells & fight viruses

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Fighting viral infections

Tumor surveillance

Primary functions of natural killer cells

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T & B Cells

Adaptive cells

Go through formal selection process (Clonal selection)

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Bone marrow

Large reserves of neutrophils are stored in the [?] & are released when needed

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Macrophages

As neutrophils die in the tissue after killing bacteria, they are then engulfed and degraded by [?]

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Dead neutrophils

Pus is composed primarily of [?]

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Binding of bacteria to phagocytic receptors on macrophages

What induces the engulfment & degradation of bacteria

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Phagosome

Membrane-bound sac that forms around foreign pathogens during phagocytosis

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Phagolysosome

Cytoplasmic body formed by the fusion of a phagosome and lysosome during phagocytosis in order to destroy engulfed pathogens

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Synthesis & release of cytokines & initiation of inflammatory response

The binding of components of bacteria to signaling receptors on macrophages induces what?

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Antibody

Structures on the surface of B Cells

Bind to pathogens & cause them to be inactivated or destroyed

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<p>Antigen-binding site</p><p>Variable regions</p><p>Constant regions</p><p>Transmembrane region</p>

Antigen-binding site

Variable regions

Constant regions

Transmembrane region

Top to bottom: Structures on the surface of B (antibodies) and T cells (T-Cell Receptor)

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Antigen

Part of pathogen

Triggers immune response when binging to antibody

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Effector cells - Plasma cells

Memory cells

Clonal Selection: B Cell + Antigen =

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Effector cells - Cytotoxic T Lymphocytes (CTL) & helper cells

Memory cells

Clonal Selection: T Cell + Antigen =

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Cytotoxic T Lymphocyte

Produced after T cells discover an antigen

Killer cells

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Plasma Cells

Produced when B cells encounter antigens

Make antibodies

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<ol><li><p>Toxin attaches to cell w/ receptors for toxin</p></li><li><p>Neutralization - Antibodies surround toxins</p></li><li><p>Antibodies w/ toxins gather near surface of phagocyte, leading to ingestion &amp; destruction of toxins</p></li></ol><p></p>
  1. Toxin attaches to cell w/ receptors for toxin

  2. Neutralization - Antibodies surround toxins

  3. Antibodies w/ toxins gather near surface of phagocyte, leading to ingestion & destruction of toxins


Antibody response to bacterial toxins

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<ol><li><p>Macrophage or dendritic cell encounter bacteria</p></li><li><p>Opsonization </p><ol><li><p>Antibodies surround the bacteria &amp; bring it closer to macrophage surface</p></li><li><p>Antibodies gather around bacteria and complement binds to bacteria</p></li></ol></li><li><p>Ingestion &amp; Destruction of bacteria</p><ol><li><p>Phagocyte surrounds bacteria w/ antibodies</p></li><li><p>Complement binds to receptors on phagocyte, anchoring the bacteria for phagocytosis</p></li></ol></li></ol><p></p>
  1. Macrophage or dendritic cell encounter bacteria

  2. Opsonization

    1. Antibodies surround the bacteria & bring it closer to macrophage surface

    2. Antibodies gather around bacteria and complement binds to bacteria

  3. Ingestion & Destruction of bacteria

    1. Phagocyte surrounds bacteria w/ antibodies

    2. Complement binds to receptors on phagocyte, anchoring the bacteria for phagocytosis


Antibody response to full bacteria in extracellular space

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Thymus

Primary lymphoid organ

Where T cells develop & mature

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Bone Marrow

Primary lymphoid organ

Where B Cells develop & mature

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Spleen

Peyer’s patches (in small intestine)

Adenoids

Tonsils

Lymph nodes

Where clonal selection happens

Secondary lymphoid organs

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Clonal selection

Secondary lymphoid organs are determined as where [?] happens

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Spleen

Where lymphocytes in the blood are circulated

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Left Subclavian vein

Where lymph drains into to return to the heart

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Lymphatic Capillaries

Structure where lymphocytes enter the tissue space

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Afferent lymphatic vessel

Where lymphocytes exit the lymph node

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Efferent lymphatic vessel

Where lymphocytes enter the lymph node

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<p>Lymphatic Capillaries</p><p>Lymphatic vessels</p><p>Lymphoid follicle</p><p>Afferent lymphatic vessel</p><p>Secondary follicle</p><p>Germinal center</p><p>Efferent lymphatic vessel</p>

Lymphatic Capillaries

Lymphatic vessels

Lymphoid follicle

Afferent lymphatic vessel

Secondary follicle

Germinal center

Efferent lymphatic vessel

Lymph node structures

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is not an antigen

The lymphocyte leaves the lymph node when there [is/is not] an antigen

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Valves

There are [?] along the afferent and efferent lymphatic vessels to prevent backflow

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Secondary lymphoid tissues

Adaptive immunity is initiated in [?]

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<p>Dendritic cells carrying pathogens</p>

Dendritic cells carrying pathogens

The adaptive immune response is activated by [?] being drained into the lymph node

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Paracortex

In the lymph node, the T-cell area is called the [?]

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Cortex

In the lymph node, the B-cell area is called the [?]

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Germinal Center

Active center of B cell activity in the lymph node

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Medullary Sinus

In the lymph node, Plasma cells mostly reside in the [?]

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<p>Lymphoid follicle/cortex (B-cell area)</p><p>Medullary sinus</p><p>Paracortex/T-cell area</p><p>Germinal center</p><p>Marginal Sinus</p><p>Afferent &amp; Efferent lymphatic vessels</p><p>Artery &amp; Vein</p>

Lymphoid follicle/cortex (B-cell area)

Medullary sinus

Paracortex/T-cell area

Germinal center

Marginal Sinus

Afferent & Efferent lymphatic vessels

Artery & Vein

Structures of the Lymph node

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Tissue

Lymph nodes drain [?] of pathogens

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Blood

Spleen drains [?] of pathogens

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Get rid of old RBCs

Start immune response

Functions of the Spleen

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White pulp

[?] of the spleen initiates immune responses

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Red pulp

[?] of the spleen is where RBCs are destroyed

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B-Cell corona - young

Germinal center - mature

Area where B-cells are in the white pulp of the spleen

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Periarteriolar lymphoid sheath

Area where T-cells are in the white pulp of the spleen

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<p>Perifollicular zone</p><p>Marginal zone</p><p>B-Cell Corona</p><p>Germinal Center</p><p></p><p>Central arteriole</p><p>Periarteriolar lymphoid sheath</p>

Perifollicular zone

Marginal zone

B-Cell Corona

Germinal Center


Central arteriole

Periarteriolar lymphoid sheath

Structure of the white pulp of spleen

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M cell

Dendritic cells

In the gut, antigens get into lymphoid tissue through the [?] in the epithelium surrounding the gut lumen, activating [?]

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Efferent lymphatic vessels to a larger lymph nodes

Gut-associated lymphoid tissues drain through the [?]

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Opsonization

Coating of antibodies on pathogen facilitate phagocytosis by attaching to receptors on phagocytes

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Neutralization

Antibodies bind tightly to a site on a pathogen to inhibit its growth, replication, or interaction with human cells

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Tonsils

Adenoids

Appendix

Peyer’s patches

Gut-Associated Lymphoid Tissues