Protective Immune Response Polarize Again Extracellular Bacterial Pathogen

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MICROBIOLOGY AND IMMUNOLOGY MOBILE  -  IMMUNOLOGY Affiliate NINE

CELLS INVOLVED IN IMMUNE RESPONSES AND ANTIGEN RECOGNITION

I. OVERVIEW

The immune system has developed to protect the host from pathogens and other foreign substances. Self/non-self discrimination is one of the hallmarks of the immune system. There are two mains sites where pathogens may reside: extracellularly in tissue spaces or intracellularly within a host cell, and the immune arrangement has different means of dealing with pathogens at these sites.

A. Extracellular pathogens
Antibodies are the main defense against extracellular pathogens and they function in three major means:

ane. Neutralization (Figure 1a)
By binding to the pathogen or foreign substance antibodies can block the association of the pathogen with their targets. For example, antibodies to bacterial toxins can prevent the binding of the toxin to host cells thereby rendering the toxin ineffective. Similarly, antibody binding to a virus or bacterial pathogen can block the attachment of the pathogen to its target jail cell thereby preventing infection or colonization.
2. Opsonization (Figure 1b)
Antibody binding to a pathogen or strange substance tin can opsonize the material and facilitate its uptake and devastation past phagocytic cells. The Fc region of the antibody interacts with Fc receptors on phagocytic cells rendering the pathogen more readily phagocytosed.
3. Complement activation (Effigy 1c)
Activation of the complement pour by antibody can effect in lysis of certain bacteria and viruses. In add-on, some components of the complement pour (due east.1000. C3b) opsonize pathogens and facilitate their uptake via complement receptors on phagocytic cells.

B. Intracellular pathogens
Considering antibodies do not get into host cells, they are ineffective against intracellular pathogens. The allowed system uses a dissimilar arroyo to deal with these kinds of pathogens. Cell-mediated responses are the master defense force against intracellular pathogens and the approach is different depending upon where the pathogen resides in the host cell (i.e., in the cytosol or within vesicles). For example, most viruses and some bacteria reside in the cytoplasm of the host jail cell, however, some bacteria and parasites really live within endosomes in the infected host prison cell. The primary defense against pathogens in the cytosol is the cytotoxic T lymphocyte (Tc or CTL). In dissimilarity, the primary defense against a pathogen within vesicles is a subset of helper T lymphocytes (Th1).

1. Cytotoxic T lymphocytes (Figure 2)
CTLs are a subset of T lymphocytes that express a unique antigen on their surface chosen CD8. These cells recognize antigens from the pathogen that are displayed on the surface of the infected cell and kill the jail cell thereby preventing the spread of the infection to neighboring cells. CTLs impale past inducing apoptosis in the infected cell.

2.  Th1 Helper T cells (Figure 3)
Thursday cells are a subset of T cells that limited a unique antigen on their surface called CD4. A subpopulation of Th cells, Th1 cells, is the master defense force against intracellular pathogens that live within vesicles. Th1 cells recognize antigen from the pathogen that are expressed on the surface of infected cells and release cytokines that actuate the infected cell. Once activated, the infected cell can then impale the pathogen. For instance, Mycobacterium tuberculosis, the causative agent of tuberculosis, infects macrophages but is not killed considering it blocks the fusion of lysosomes with the endosomes in which it resides. Th1 cells that recognize M. tuberculosis antigens on the surface of an infected macrophage tin secrete cytokines that activate macrophages. In one case activated the lysosomes fuse with endosomes and the One thousand. tuberculosis leaner are killed.

Although immune responses are tailored to the pathogen and to where the pathogen resides, most pathogens tin arm-twist both an antibody and a cell-mediated response, both of which may contribute to ridding the host of the pathogen. However, for whatsoever particular pathogen an antibody or a cell-mediated response may be more important for defense against the pathogen.

II. Cells of the Immune Organisation

All cells of the immune system originate from a hematopoietic stem cell in the os marrow, which gives rise to two major lineages, a myeloid progenitor cell and a lymphoid progenitor jail cell (Figure 4). These 2 progenitors requite rise to the myeloid cells (monocytes, macrophages, dendritic cells, meagakaryocytes and granulocytes) and lymphoid cells (T cells, B cells and natural killer (NK) cells), respectively. Theses cells make up the cellular components of the innate (not-specific) and adaptive (specific) immune systems.

A. Cells of the innate immune system

Cells of the innate allowed organization include phagocytic cells (monocyte/macrophages and PMNs), NK cells, basophils, mast cells, eosinophiles and platelets. The roles of these cells have been discussed previously (see non-specific immunity, lecture ane). The receptors of these cells are pattern recognition receptors (PRRs) that recognize broad molecular patterns found on pathogens (pathogen associated molecular patterns, PAMPS).

B. Cells that link the innate and adaptive immune systems

A specialized subset of cells called antigen presenting cells (APCs) are a heterogenous population of leukocytes that play an of import role in innate immunity and also act every bit a link to the adaptive immune organization by participating in the activation of helper T cells (Th cells). These cells include dendritic cells and macrophages. A characteristic characteristic of APCs is the expression of a cell surface molecule encoded by genes in the major histocompatibility circuitous, referred to as class 2 MHC molecules. B lymphocytes also express form 2 MHC molecules and they also office as APCs, although they are not considered as part of the innate allowed system. In addition, sure other cells ( east.one thousand., thymic epithelial cells) tin can express course 2 MHC molecules and can function as APCs.

C. Cells of the adaptive immune system

Cells that make upwardly the adaptive (specific) allowed system include the B and T lymphocytes. After exposure to antigen, B cells differentiate into plasma cells whose primary function is the production of antibodies. Similarly, T cells can differentiate into either T cytotoxic (Tc) or T helper (Thursday) cells of which there are 2 types Th1 and Th2 cells.
There are a number of jail cell surface markers that are used in clinical laboratories to distinguish B cells, T cells and their subpopulations. These are summarized in Table 1.

Table one. Main distinguishing markers of T and B cells
Marking	B cells	Tc	Th
CD3	-	+	+
CD4	-	-	+
CD8	-	+	-
CD19 and/or CD20	+	-	-
CD40	+	-	-
Ag receptor	BCR (surface Ig)	TCR	TCR

III. Specificity of the Adaptive Allowed Response

Specificity on the adaptive immune response resides in the antigen receptors on T and B cells, the TCR and BCR, respectively. The TCR and BCR are like in that each receptor is specific for 1 antigenic determinant but they differ in that BCRs are divalent while TCRs are monovalent (Effigy 5). A consequence of this difference is that while B cells tin can have their antigen receptors cantankerous-linked by antigen, TCRs cannot. This has implications every bit to how B and T cells can get activated.

Each B and T cells has a receptor that is unique for a particular antigenic determinant and there are a vast array of different antigen receptors on both B and T cells. The question of how these receptors are generated was the major focus of immunologists for many years. Two basic hypotheses were proposed to explain the generation of the receptors: the instructionist (template) hypothesis and the clonal selection hypothesis.

A. Instructionist hypothesis

The instructionist hypothesis states that in that location is but one mutual receptor encoded in the germline and that different receptors are generated using the antigen as a template. Each antigen would cause the 1 common receptor to be folded to fit the antigen. While this hypothesis was elementary and very appealing, it was non consistent with what was known about protein folding (i.e. poly peptide folding is dictated past the sequence of amino acids in the poly peptide). In improver this hypothesis did not account for self/non-self discrimination in the immune system. It could not explain why the one common receptor did not fold around self antigens.

B. Clonal selection hypothesis

The clonal selection hypothesis states that the germline encodes many different antigen receptors - one for each antigenic determinant to which an individual volition be capable of mounting an immune response. Antigen selects those clones of cells that have the appropriate receptor. The four bones principles of the clonal selection hypothesis are:

ane. Each lymphocyte bears a single type of receptor with a unique specificity.
2. Interaction between a foreign molecule and a lymphocyte receptor capable of binding that molecule with a loftier affinity leads to lymphocyte activation.
3. The differentiated effector cells derived from an activated lymphocyte volition carry receptors of an identical specificity to those of the parental cell from which that lymphocyte was derived.
4. Lymphocytes bearing receptors for self molecules are deleted at an early stage in lymphoid prison cell development and are therefore absent from the repertoire of mature lymphocytes.

 The clonal pick hypothesis is now generally accustomed as the right hypothesis to explicate how the adaptive immune system operates.  It explains many of the features of the immune response: ane) the specificity of the response; 2) the signal required for activation of the response (i.east. antigen); three) the lag in the adaptive allowed response (fourth dimension is required to activate cells and to expand the clones of cells); and 4) self/not-self discrimination.

4. Lymphocyte Recirculation

Since there are relatively few T or B lymphocytes with a receptor for any detail antigen (1/x,000 – 1/100,000), the chances for a successful encounter betwixt an antigen and the appropriate lymphocyte are slim. Nonetheless, the chances for a successful encounter are greatly enhanced by the recirculation of lymphocytes through the secondary lymphoid organs. Lymphocytes in the blood enter the lymph nodes and percolate through the lymph nodes (Figure six). If they do non encounter an antigen in the lymph node, they leave via the lymphatics and return to the blood via the thoracic duct. It is estimated that ane-two% of lymphocytes recirculate every hour. If the lymphocytes in the lymph nodes come across an antigen, which has been transported to the lymph node via the lymphatics, the cells become activated, divide and differentiate to get a plasma jail cell, Thursday or Tc cell. After several days the effector cells can leave the lymph nodes via the lymphatics and return to the blood via the thoracic duct and then make their way to the infected tissue site.

Naive (virgin) lymphocytes enter the lymph nodes from the blood via High Endothelial Venules (HEVs) Homing receptors on the lymphocytes directly the cells to the HEVs. In the lymph nodes, lymphocytes with the appropriate antigen receptor encounter antigen, which has been transported to the lymph nodes by dendritic cells or macrophages. After activation the lymphocytes limited new receptors that allow the cells to leave the lymph node and reenter the circulation. Receptors on the activated lymphocytes recognize cell adhesion molecules expressed on endothelial cells near the site of an infection and chemokines produced at the infection site help attract the activated cells (Figure 7).

IMMUNITY: CONTRASTS Between Non-SPECIFIC AND SPECIFIC

A. Non-specific (natural, native, innate)

ane. Organization in place prior to exposure to antigen
2. Lacks bigotry amidst antigens
3. Tin be enhanced after exposure to antigen through effects of cytokines

B. Specific (caused, adaptive)

1. Induced by antigen
2. Enhanced past antigen
3. Shows fine discrimination

The hallmarks of the specific immune organisation are retention and specificity.
1. The specific immune system "remembers" each encounter with a microbe or strange antigen, so that subsequent encounters stimulate increasingly effective defence mechanisms.
2. The specific allowed response amplifies the protective mechanisms of non-specific immunity, directs or focuses these mechanisms to the site of antigen entry, and thus makes them amend able to eliminate foreign antigens.

CELLS OF THE Allowed Organization

All cell types in the allowed system originate from the bone marrow.
In that location are two chief lineages that derive from the hemopoietic stem cell:

1. the lymphoid lineage
T lymphocytes (T cells)
B lymphocytes (B cells)
Natural killer cells (NK cells)

2. the myeloid lineage
Monocytes, macrophages
Langerhans cells, dendritic cells
Megakaryocytes
Granulocytes (eosinophils, neutrophils, basophils)

Clonal choice The four bones principles of the clonal selection hypothesis

Each lymphocyte bears a single type of receptor of a unique specificity

Interaction between a strange molecule and a lymphocyte receptor capable of bounden that molecule with high affinity leads to lymphocyte activation

The differentiated effector cells derived from an activated lymphocyte volition conduct receptors of an identical specificity to those of the parental cell from which that lymphocyte was derived

Lymphocytes bearing receptors specific for self molecules are deleted at an early on stage in lymphoid cell development and are therefore absent from the repertoire of mature lymphocytes

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Source: https://microbiologybook.org/mobile/m.immuno-9.htm

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