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ANUSHI JAIN
ROLL NO : 12
PAPER 2
MSC I
The Complement
System
INTRODUCTION
• The complement system is a group of serum
proteins, which participate in innate as well as
adaptive immune response.
• The complement system is characteristically
activated by the antigen-antibody interaction.
• It helps antibacterial cells and molecules of the
immune system.
PATHWAYS
 The complement system can be activated by three
ways :
1. CLASSICAL PATHWAY
2. ALTERNATIVE PATHWAY
3. LECTIN PATHWAY
The complement system
COMPONENTSClassicalPathway
• C1 (C1q,C1r,C1s)
• C2 (C2a,C2b)
• C3(C3a,C3b)
• C4(C4a,C4b)
AlternativePathway
• C3 (C3a,C3b)
• Factor B
(B,Ba,BB)
• Factor D
• Properdin
MembraneAttackComplex
• C5 (C5a,C5b)
• C6
• C7
• C8
• C9
BIOLOGICAL CONSEQUENCES
Complement system serves as an important mediator of
the humoral response , It plays a major role in host
defense through destruction of invading
micro0organisms.
 The Membrane-Attack Complex (MAC) mediates cell
lysis.
 The split products or the active forms of the
components of the complement participate in
Inflammatory response , Opsonization of antigen ,
viral neutralization and clearance of the immune
complexes.
1. CELL LYSIS
 The membrane-attack complex (MAC) formed by
complement activation can lyse gram-negative bacteria ,
parasites , viruses , erythrocytes , and nucleated cells.
 Gram-positive bacteria are generally resistant to the
complement mediated lysis because of thick peptidoglycan
layer in their cell wall which prevents the insertion MAC
into their inner membrane.
 The complement system lyses these target cells through
the alternative pathway and lectin (MBL) pathway in
absence of antibodies and through the classical pathway in
the presence of antibodies.
 MAC formed forms a pore in the cells and disturbs the
osmotic balance of the cell and ultimately destroys it.
 Lysis of nucleated cells require multiple MACs ,
whereas lysis of RBC requires single MAC.
 If MAC is removed in time ,the cells are capable of
repairing the damage and restoring its osmotic
stability.
The complement system
The complement system
2. INFLAMMATION
 Inflammation is the most important
consequence of the complement activation.
 C3a , C4a and C5a act as anaphylatoxins , i.e.
, they cause smooth muscles to contract.
 C5a and C3a act as chemoattractants , i.e. ,
they effect the motility of the cells.
3.OPSONIZATION
 It’s a process in which bacteria and other cells
are altered in such a manner that they are
more readily engulfed by the phagocytes.
 C3b is a major opsonin and the receptors for
C3b are CR1 , CR3 and CR4.
The complement system
4. VIRAL NEUTRALIZATION
 Viral neutralization means neutralization of viral
infectivity.
 There are various ways by which viruses can be neutralized
:
A. Formation of larger viral aggregates
 Reduces the net number of infectious viral particles.
B. Coating of a antibody and/or complement (Cb3) to
the surface of the viral particle
 Blocking attachment to host cells
 Binding of binding particle to cells possessing CR1
receptor or Fc.
 Lysing most enveloped viruses.
The complement system
5. CLEARANCE OF IMMUNE COMPLEXES
 Erythrocytes plays an important role in clearance of the
immune complexes.
 The coating of the soluble immune complexes with C3b
facilitates their binding to the CR1.
 This interaction between CR1 and C3b results in adherence
of immune complexes to the erythrocytes.
 Erythrocytes carry these immune complexes to the spleen
and liver ; wherein these immune complexes are removed
from erythrocytes and phagocytosed.
 The importance of clearing immune complexes can be
seen in patients with autoimmune disease Systemic
Lupus Erythematosus.
The complement system
The complement system
The complement system
THANK YOU!

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The complement system

  • 1. ANUSHI JAIN ROLL NO : 12 PAPER 2 MSC I The Complement System
  • 2. INTRODUCTION • The complement system is a group of serum proteins, which participate in innate as well as adaptive immune response. • The complement system is characteristically activated by the antigen-antibody interaction. • It helps antibacterial cells and molecules of the immune system.
  • 3. PATHWAYS  The complement system can be activated by three ways : 1. CLASSICAL PATHWAY 2. ALTERNATIVE PATHWAY 3. LECTIN PATHWAY
  • 5. COMPONENTSClassicalPathway • C1 (C1q,C1r,C1s) • C2 (C2a,C2b) • C3(C3a,C3b) • C4(C4a,C4b) AlternativePathway • C3 (C3a,C3b) • Factor B (B,Ba,BB) • Factor D • Properdin MembraneAttackComplex • C5 (C5a,C5b) • C6 • C7 • C8 • C9
  • 6. BIOLOGICAL CONSEQUENCES Complement system serves as an important mediator of the humoral response , It plays a major role in host defense through destruction of invading micro0organisms.  The Membrane-Attack Complex (MAC) mediates cell lysis.  The split products or the active forms of the components of the complement participate in Inflammatory response , Opsonization of antigen , viral neutralization and clearance of the immune complexes.
  • 7. 1. CELL LYSIS  The membrane-attack complex (MAC) formed by complement activation can lyse gram-negative bacteria , parasites , viruses , erythrocytes , and nucleated cells.  Gram-positive bacteria are generally resistant to the complement mediated lysis because of thick peptidoglycan layer in their cell wall which prevents the insertion MAC into their inner membrane.  The complement system lyses these target cells through the alternative pathway and lectin (MBL) pathway in absence of antibodies and through the classical pathway in the presence of antibodies.
  • 8.  MAC formed forms a pore in the cells and disturbs the osmotic balance of the cell and ultimately destroys it.  Lysis of nucleated cells require multiple MACs , whereas lysis of RBC requires single MAC.  If MAC is removed in time ,the cells are capable of repairing the damage and restoring its osmotic stability.
  • 11. 2. INFLAMMATION  Inflammation is the most important consequence of the complement activation.  C3a , C4a and C5a act as anaphylatoxins , i.e. , they cause smooth muscles to contract.  C5a and C3a act as chemoattractants , i.e. , they effect the motility of the cells.
  • 12. 3.OPSONIZATION  It’s a process in which bacteria and other cells are altered in such a manner that they are more readily engulfed by the phagocytes.  C3b is a major opsonin and the receptors for C3b are CR1 , CR3 and CR4.
  • 14. 4. VIRAL NEUTRALIZATION  Viral neutralization means neutralization of viral infectivity.  There are various ways by which viruses can be neutralized : A. Formation of larger viral aggregates  Reduces the net number of infectious viral particles. B. Coating of a antibody and/or complement (Cb3) to the surface of the viral particle  Blocking attachment to host cells  Binding of binding particle to cells possessing CR1 receptor or Fc.  Lysing most enveloped viruses.
  • 16. 5. CLEARANCE OF IMMUNE COMPLEXES  Erythrocytes plays an important role in clearance of the immune complexes.  The coating of the soluble immune complexes with C3b facilitates their binding to the CR1.  This interaction between CR1 and C3b results in adherence of immune complexes to the erythrocytes.  Erythrocytes carry these immune complexes to the spleen and liver ; wherein these immune complexes are removed from erythrocytes and phagocytosed.  The importance of clearing immune complexes can be seen in patients with autoimmune disease Systemic Lupus Erythematosus.