The third line of defense is a component of adaptive immunity which has a specific immune response and form immunological memory.
Initiation
of adaptive immunity:
·
The third line of defense comes into action
when antigen presenting cells (APCs) engulf the pathogens and display the
pathogenic antigens on their specific markers called MHC class II markers.
·
APCs then travel via the lymphatic system
into the lymph nodes where helper T cells are present.
·
Antigens on APCs interact with T cell
receptors on helper T cells to make them active.
The activated helper T cells
then initiate the adaptive immune response via humoral or cell mediated immune
response.
1. Humoral
immunity:
Humoral immunity involves
the destruction of pathogens by producing antibodies against specific
pathogenic antigens. A type of white blood cells known as B lymphocytes has B
cell receptors on their surface known as antibodies.
·
B cell lymphocytes become activated when
their antibodies interact with antigens. Antigens bind to their complementary
site known as antigen-binding site on an antibody and the respective B cell is
said to be “selected”. The selection of B cell together with helper T cell is
termed as “clonal selection theory”.
·
Both B cell and helper T cell have
complementary receptor to the antigen. The selected helper T cell interacts
with selected B cell and secretes cytokines to stimulate “clonal expansion”
where multiple copies of B cells are produced. Cytokines also stimulates the
differentiation of B cell into B memory cells and effector cells.
·
After differentiation, the effector cells
also known as plasma cells release antibodies into the bloodstream to defend
against a specific antigen whereas, the memory B cells participate in
immunological memory and remain in blood for an extended period until the
specific antigen is introduced in the body again.
2. Cell-mediated
immunity:
·
During the selection of T helper cell there
is another type of cell known as naive T cell which interacts with antigen
presenting cell and becomes “selected”. Cytokines released from helper T cell
stimulate clonal expansion and differentiation.
·
In clonal expansion, multiple copies of T
cells are produced and differentiated into two types of cells i.e. effector
cell and memory T cell.
·
The effector cell also known as cytotoxic T
cell reaches the site of infection and interacts with abnormal or infected cell
that is presenting the specific antigen complementary to the T cell receptor.
Upon binding of antigen to T cell receptor of cytotoxic T cell, a chemical
called perforin is released by cytotoxic T cell which causes apoptosis or
programmed cell death.
· Memory T cells remain in blood for a long period of time and help in creating immunological memory to defend against the pathogen when it re-enters the body in future.