Skip to main content

Specific Immunity


1.     Development of Lymphocyte specificity/receptors

A. Acquired immunity involves the reactions of B and T lymphocytes to foreign molecules, or antigens. Before they can react, each lymphocyte must undergo differentiation into its final functional type by developing protein receptors for antigen, the specificity of which is genetically controlled and unique for each type of lymphocyte.
B. The Clonal selection theory explains this process. Genetic recombination and mutation during embryonic and fetal development produce billions of different lymphocyte clones, each bearing a different receptor. This provides a huge lymphocyte repertoire required to react with antigens. 
C.  Tolerance to self, the elimination of any lymphocytes clone that can attack self, occurs during this time.
D. The receptors on B cells are immunoglobulin (Ig) molecules, and receptors on t cells are smaller glycoprotein molecules.
E. Other receptors needed in recognition are governed by the major histocompatibility (MHC) gene complex, which is also referred to as the human leukocyte antigen (HLA) complex.
F. Expression of these genes gives rise to receptors on most cells that govern cell communication and recognition of self and antigens.
G. B-cells maturation: Immature B stem cells originate in the yolk sac, liver, and bone marrow and differentiate into mature cells under the influence of special stromal cells in the bone marrow. Mature cells acquire Ig receptors and home to predetermined sites in lymphoid organs, ready to react with antigen.
H. T-cells maturation: Immature T stem cells originate in the same areas of the embryo and fetus but mature under the influence of the thymus gland. Specificity is acquired through addition of CD (cluster designation) receptors, and mature cells home to different sites in lymphoid organs.
2.     Introduction of Antigen/Immunogens
A.   An antigen (Ag) is any substance that stimulates an immune response.
-       Requirement for antigenicity include foreignness (recognition as nonself), large size, and complexity of cell or molecules.
-       Foreign cells and large complex molecules (over 10,000 MW) are most antigenic.
-       Foreign molecules less than 1,000 MW (Haptens) are not antigenic unless attached to a larger carrier molecule.
-       The antigenic determinant is small molecules group of the foreign substance that is recognized by lymphocytes. Cells, viruses and large molecules can have numerous antigenic determinants.

B.    Special categories of antigens include:
-       Autoantigens, molecules on self tissues for which tolerance is adequate.
-       Alloantigens, cells surface markers of one individual that are antigens to another of that same species.
-       Heterophilic antigens, molecules from unrelated species that bear similar antigenic determinant.
-       Superantigens, complex bacterial toxins.
-       Allergen, the antigen that provokes allergy.
3.     Cooperation in Immune reactions to antigen
A.     T-cell-dependent antigens must be processed by large phagocytes such as dendritic cells or macrophages calls antigen-presenting cells (APCs). An APC alters the antigen and attaches it to its MHC receptor for presenting to lymphocytes.
B.     The presentation of a single antigen involves a direct collaboration between and APC, a T helper (TH), and an antigen specific B or T cells.
C.     Cytokines involved are interleukin-1 from the APC which activates the TH cells, and interleukin-2 produces by TH cell, which activates B and other T cells.

4.     B-cells activation and antibody production
A.     Once B cells process the antigen, interact with TH cells, and are stimulated by B-cell growth and differentiation factors, they enter the cell cycle in preparation for mitosis and clonal expansion.
B.     Divisions give rise to plasma cells that secrete antibodies and memory cells that can react to that same antigen later.
-       Nature of Antibodies (immunoglobulins): A single immunoglobulin molecule (monomer) is large Y-shaped protein molecule consisting of four polypeptide chains. It contains two identical fragment (Fab) with ends that form the active site that binds with a unique specificity to an antigen. The single fragment of the antibody (Fc) binds to self.
-       Antigen-Antibody (Ag-Ab) recognitions include opsonization, neutralization by antitoxin, agglutination, and complement fixation.
·      The Fc portion can bind to various body cells and mediate inflammation and allergy. 
-       The five antibody classes, which differ in size and function, are IgG, IgA (secretory Ab), IgM, IgD, IgE. 
-       Antibodies in Serum (Antiserum):
·      Serum antibodies can be identified through electrophoresis and quantified by testing the titer (levels of antibodies) over time.
·      The first introduction of an Ag to the immune system produces a primary response, with a gradual increase in Ab titer.
·      The second contact with the same Ag produces a secondary, or anamnestic, response, due to memory cells produced during initial response.
5.     T-cells and Cell-mediated Immunity (CMI
-       Monoclonal antibodies (MAB), response, due to memory cells antibodies formed by using a mouse B cell with a cancer cell. MABs are used in diagnosis of disease, identified of microbes, and therapy. 
A.     T cells act directly against antigens and foreign cells. T cells secrete cytokines (interleukin, interferon, lymphotoxins) that act on other cells. Sensitized T cells proliferate into long-lasting memory T cells and one of the following depending upon its CD receptor:
-       Cytotoxic (Tc) or CD8 cells destroy complex foreign or abnormal cells by forming perforins that lyse the cell.
-       Delayed hypersensitivity cells (TD) cause a form of hypersensitivity.
-       T suppressor cells (Ts) limit the actions of other T cells and B cells.
6.     Classification of Acquired Immunity
A.     Immunities acquired through B and T lymphocytes can be classified by a simple system.
-       Natural immunity is acquired as part of normal life experiences.
-       Artificial immunity is acquired through medical procedures such as immunization.
-       Active immunity, results when a person is challenged with antigen that stimulates production of antibodies. It creates memory, takes time and is lasting.
-       In passive immunity, preformed antibodies are donated to an individual. It does not create memory, acts immediately, and is short term.
B.     Combination of acquired immunity are:
-       Natural actives, acquired upon infection and recovery, and natural passive, acquired by a child through placenta and breast milk.
-       Artificial active (vaccination), acquired through inoculation with a selected antigen, and artificial passive, administration of immune serum or globulin. 


Comments

Popular posts from this blog

ក្រមសីលធម៌ឱសថការី

ក្រមសីលធម៌ឱសថការី ១​​.​ និយមន័យក្រមសីលធម៌វិជ្ជាជីវៈឱសថ? ចំ​​ៈ គឺជាកាតព្វកិច្ចដែលឱសថការីត្រូវបំេពញ ចំពោះអតិថិជន សហការី អ្នកផ្តល់សេវា​ខាភិបាល និស្សិត វិជ្ជាជីវៈ និង​ អាជ្ញាធរមានសមត្ថកិច្ចក្នុងការអនុវត្តវិជ្ជាជីវៈឱសថ។​ ២. លក្ខណៈខុសគ្នារវាង ក្រមសីមធម៌វិជ្ជាជីវៈ​ និង​និតិក្រម? ចំៈ​ មាន៣ចំនុចៈ - ការរៀបចំ៉ ( development) ៖ ក្រមសីលធម៌ត្រូវបានរៀបចំដោយគណៈឱសថការីកម្ពុជា ( pharmacy professional ethic) រីនិតិក្រមត្រូវបានរៀបចំដោយស្ថាប័ននិតិបញ្ញត្តិ ឬស្ថាប័ននិតិប្រតិបត្តិ - ដែននៃការអនុវត្ត ( the field of implementation) ៖ ក្រមសីធម៌វិជ្ជាជីវៈត្រូវអនុវត្តចំពោះតែឱសថការីណាដែលប្រកបវិជ្ជាជីវៈឱសថ រីនិតិក្រមត្រូវអនុវត្តចំពោះរូបវ័ន្តបុគ្គល ( Physical person) និងនិតិបុគ្គល (ស្ថាប័នឬក្រសួង.. ) - ទោសបញ្ញត្តិ ការប្រព្រឹត្តល្មើសនិងក្រមសីលធម៌វិជ្ជាជីវៈ​​ ត្រូវទទួលទោសដែលមានលក្ខណៈជាអង្គការវិន័យ​ ដែលវិនិច្ឆ័យដោយ ក្រុមប្រឹក្សាគណៈឱសថការី​ ដូចជាការស្តីបន្ទោស ការប្រមានជាលាយ លក្ខអក្សរ ការផ្ជួរសមាជិកភាពជាបណ្តោះ អាសន្ន និង​ការដកហូតសមាជិកភាពជាអចិន្ត្រៃ៌។​ រីការប្រព្រឹត្តល្មើសនិងនិតិក្រមត្រូវផ្តន្ទាទោសដែលមានលក្ខណៈជា...

The major events in Inflammation

This is the animation of acute inflammation response: 

ការផ្តល់ដង្ហើមសិប្បសិម្មិត

របៀបផ្តល់ដង្ហើមសិប្បនិមិ្មត អ្នកនឹងអាចជួបនូវហេតុការណ៌ជាយថាហេតុដែលតម្រូវអោយអ្នកធ្វើការសង្គ្រោះជនរងគ្រោះជា បន្ទាន់តាមដែលអ្នកអាចធ្វើ​ បាន! ការរផ្តល់ដង្ហើមសិប្បនិម្មិត គេអាចធ្វើសូម្បីតែនៅពេលជនរងគ្រោះនៅដង្ហើមខ្សោយផ្តឹកៗមិនទាន់ ដាច់ខ្យល់ក៏អាចធ្វើបានដែរ។​ នៅពេលអ្នកផ្តល់ដង្ហើមសិប្បនិម្មិត អ្នកត្រូវផ្លុំខ្យល់ដង្ហើមចេញអោយ ស្របនិងការដកដង្ហើមរបស់ជនរងគ្រោះ។​ ជំហានទី១ ·        ដាក់ជនរងគ្រោះអោយដេកផ្ងា មុខឡើងលើ ·        ការឆ្លើយតប-តើជនរងគ្រោះដឹងខ្លួនរឺទេ? ·        ពិនិត្យមើលចលនាដើមទ្រូងដាក់ត្រចៀករបស់អ្នកលើមាត់របស់ជនរងគ្រោះ ដើម្បីពិនិត្យមើលដង្ហើម។​ ·        ហៅរកជំនួយ។​ ជំហានទី២ លើកចង្កាឡើង បើសិន ក​ ជនរងគ្រោះគ្មានរបួស ·        ផ្អៀងក្បាលជនរងគ្រោះដើម្បី “ ហិតក្លិន ” (មានក្លិនអ្វីចេញមករឺទេ) ដោយយកដៃម្ខាង ទៀតទ្រ ក របស់គាត់ចុះ ក្រោម។​ ·        សង្កត់អណ្តាត និង​ចង្ការបស់ជនរងគ្រោះនៅចន្លោះម្រាមដៃរបស់អ្នក រួចជូតសំអាត វត្ថុ...