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Module 2.1 and 2.

2: Intro to Immunology and Serology


Immunology
 The study concern with the processes by which
all living organism defends themselves against
infection.
 This is the study of our immune system that
protects our body from foreign invaders.
 This is the study of host reaction when foreign
antigens are introduced to the body.
Antigens
 short term for Antibody generators.
 Foreign substances that induce a host
response.
Immunity
 Condition of being resistant to infection.
WHEN TO USE SEROLOGY:
1. Unable to culture infectious agents
2. Confirmation of etiologic agent
identification (ID)
3. Diagnosis of immunologically related
disorder
4. Determine the immune status
HISTORICAL PERSPECTIVE
1500 AD
 Chinese practice where children were
compelled to inhale a powder – a process
known as insufflation – made from a crust
of lesions from individuals recovering from
smallpox.
 15th century – powdered smallpox “crusts”
were inserted with a pin into the skin.
 Variolation carried out by inserting or
rubbing the powdered smallpox scabs or
fluid from pustules into superficial scratches
made in the skin.
MODULE 2.5: THE LYMPHOID SYSTEM 1. Mucosal associated lymphoid tissue (MALT)
Lymphoid System o Tonsils
 Kidney - Glomerulonephritis
 Composed of two parts: Primary and secondary
 Heart - Rheumatic Heart Fever
lymphoid organs.
(RHF)
Lymphatic System
o Peyer’s patches within small intestine
 Involves lymphatic vessels, capillaries, lymph o Vermiform appendix
Bone Marrow  Fecaliths – can obstruct the
 Hematopoietic stem cells/parent cells are appendix, leading to
produced. appendicitis. (Ex. Tomato seeds,
 Center for antigen-independent lymphopoiesis chili seeds)
Thymus 2. Cutaneous (skin/epidermis) – associated
lymphoid tissue
 Found in the thorax or chest cavity o Intraepidermal lymphocytes
 Right below the thyroid gland CLASSES OF LYMPHOCYTES
 Overlying the heart
 Undergoes atrophy – decrease in size Location
 First presume in life and produces virgin T- T-cells
lymphocytes in the entire system
 Paracortical region (paracortex)
 Although thymus diminish or atrophy, it is still
o It is between follicles and medulla
capable of producing lymphocytes until at least
o Interior of secondary follicle is know as
5th or 6th decade of life (50-60 yrs old)
germinal center because it is here that
Secondary Lymphoid Organs Functions:
blasts transformation of B-cells takes
1. Trapping site of pathogens places.
2. Standby areas of T-cells, B-cells, and phagocytes B-cells
3. Place of encounter for pathogens and the cells
 Cortical region (cortex)
4. Reduction of antibodies and lymphokines and
o Specialized cells called follicular
phagocytosis occur.
5. It is antigenic-dependent lymphopoiesis dendritic cells are located here.
Spleen o It exhibits large number of receptors for
antibody and complement and hep to
 Largest secondary organ capture antigen to present to T and B
 Each day, adult blood volume passes through cells.
the spleen approximately 4 times. Lymphokines – substance produced by lymphocytes
 Found in upper-left quadrant of the abdomen, (Interferons)
just below the diaphragm
2 MAIN TYPES OF SPLENIC TISSUE: T-cells

1. Red pulp – destroys RBCs  Cell mediated immunity


2. White pulp – arranged around arterioles in a  Viral and fungal infection
periarteriolar lymphoid sheath (PALS). This  End product: Cytokines
sheath contains mainly T cells. Attached to the  Cytokines
sheath are primary follicles, which contain B o Regulates the function of lymphocytes
cells that are not yet stimulated by antigen. and other cells involve in immune
Lymph nodes response.
 Rosette formation with SRBC (CD2)
 Transit time of fluids in lymph nodes are 18hrs. B-cells
 Swelling of lymph nodes – lymphadenopathy
(sign and symptoms or monkeypox virus)  Humoral immunity
 Lymph fluid – flows slowly through spaces  Bacterial infection
called sinuses, which are lined with  End product: Antibodies
macrophages, creating an ideal location where  Surface Immunoglobulins (IgM, IgD)
phagocytosis can take place. HIV attacks T-cells because it had CD4 markers
Other Secondary Organs: T-CELL DEVELOPMENT
1. Double negative thymocyte
 Early thymocytes lack CD4 and CD8 markers
 Always under the influence of Interleukin 7 –
critical for growth and differentiation
2. Double positive thymocyte
 Thymocytes expressed both CD4 and CD8
3. Single positive T-cells
 CD4 or CD8
 They are the survivor of selection that exhibit
only one type of marker
 It will migrate to the medulla
4. Activated T-cell
5. Sensitized T-cell

 Leukemia or problems in blood and


immunocompromised patients – LOW CD4
 To test for CD4 – specimen of choice is whole
blood EDTA (purple tube – 8 to 10 inversion)
 Interleukin 1 – responsible for fever

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