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Vaishnavi Solanki
IEHE , Bhopal
2
Hybridoma is immortalized cell derived
from the fusion of B cell with a myeloma
cell ( cancerous B cell ).
Is a method for producing large numbers of identical
antibodies (also called monoclonal antibodies ).
3
• In 1975 , these technology developed by
Georges J.F. Kohler and Cesar Milstein .
• In 1984 , they shared a nobel price for this
discovery .
• The term hybridoma was coined by -
Leonard Herzenberg in 1975.
4
• The hybrid cell has the capacity of antibody
production derived from B cells.
• At the same time it can divide countinuosly by the
quality derived from Myeloma cells.
• By combining the desired qualities of both the
cells , the technology ensures large scale Antibody
production of single specificity.
5
• Monoclonal antibodies (mAb) are antibodies that are
identical because they are produced by one type of
immune cell, all clones of a single parent cell.
• Basically produced by white blood cell which is called as
plasma cell.
•MAbs are used in - treatment of cancer , transplantation
of bone marrow & organs , autoimmune diseases,
cardiovascular diseases & infectious diseases.
6
1. Immunization of specific animal which generate
hybridoma cell with spleen cell.
2. Isolation of myeloma cells .
3. Fusion between spleen cell and myeloma cell.
4. Selection of HAT medium .
5. Isolation of hybridoma cell.
6. Screening of hybridoma cell.
7
An antigen immunized to an animal (like mice) via
intravenously (direct to blood ) by injection.
Where in spleen it activate B – cell which produce
plasma cell (spleen cell ).
Plasma cell to produce monoclonal antibodies.
Isolation of plasma cell from spleen of animal.
8
 Myeloma cells are cancerous cells which is isolated from
bone – marrow .
 Myeloma cells are generally immortal in nature & has
multiplication property .
 It requires PEG (poly ethylene glycol ) medium for fusion .
 It can also done by electro fusion .
 5 different types of cells will appear :
9
( Hypoxanthine , Aminopterin , Thymidine )
• Before multiplication of Antibody , it has to synthesize new copy of DNA & for
that it requires synthesis of nucleotide.
• For synthesis of nucleotide mainly two pathways are there :
1. Salvage pathway
2. De – novo Synthesis
10
Spleen cell have
HGPRT enzyme
Myeloma cell doesn’t
have HGPRT enzyme
1. Fused plasma Present
2. Fused myeloma Absent
3. Hybridoma Present
4. Unfused plasma Present
5. Unfused myeloma Absent
HGPRT
11
12
• ELISA screening method which done by incubating
hybridoma culture in which secondary enzyme gets
conjugate & formation of colored products shows positive
hybridoma .
• Used for multiplying the hybridoma cells :
 In – vivo
 In – vitro
13
14
Serological :
• Identification of ABO blood group .
Immunopurification :
• Purification of individual interferon using monoclonal .
• Inactivation of T - lymphocytes responsible for rejection of
organ transplants.
Therapy :
• Removal of tumor cell from bone marrow.
• Treatment of acute renal failure.
• Treatment malignant leukemic cells , B cell lymphocytes , and a
variety of allograft rejections after transplantation .
15

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Hybridoma technology

  • 2. 2 Hybridoma is immortalized cell derived from the fusion of B cell with a myeloma cell ( cancerous B cell ). Is a method for producing large numbers of identical antibodies (also called monoclonal antibodies ).
  • 3. 3 • In 1975 , these technology developed by Georges J.F. Kohler and Cesar Milstein . • In 1984 , they shared a nobel price for this discovery . • The term hybridoma was coined by - Leonard Herzenberg in 1975.
  • 4. 4 • The hybrid cell has the capacity of antibody production derived from B cells. • At the same time it can divide countinuosly by the quality derived from Myeloma cells. • By combining the desired qualities of both the cells , the technology ensures large scale Antibody production of single specificity.
  • 5. 5 • Monoclonal antibodies (mAb) are antibodies that are identical because they are produced by one type of immune cell, all clones of a single parent cell. • Basically produced by white blood cell which is called as plasma cell. •MAbs are used in - treatment of cancer , transplantation of bone marrow & organs , autoimmune diseases, cardiovascular diseases & infectious diseases.
  • 6. 6 1. Immunization of specific animal which generate hybridoma cell with spleen cell. 2. Isolation of myeloma cells . 3. Fusion between spleen cell and myeloma cell. 4. Selection of HAT medium . 5. Isolation of hybridoma cell. 6. Screening of hybridoma cell.
  • 7. 7 An antigen immunized to an animal (like mice) via intravenously (direct to blood ) by injection. Where in spleen it activate B – cell which produce plasma cell (spleen cell ). Plasma cell to produce monoclonal antibodies. Isolation of plasma cell from spleen of animal.
  • 8. 8  Myeloma cells are cancerous cells which is isolated from bone – marrow .  Myeloma cells are generally immortal in nature & has multiplication property .  It requires PEG (poly ethylene glycol ) medium for fusion .  It can also done by electro fusion .  5 different types of cells will appear :
  • 9. 9 ( Hypoxanthine , Aminopterin , Thymidine ) • Before multiplication of Antibody , it has to synthesize new copy of DNA & for that it requires synthesis of nucleotide. • For synthesis of nucleotide mainly two pathways are there : 1. Salvage pathway 2. De – novo Synthesis
  • 10. 10 Spleen cell have HGPRT enzyme Myeloma cell doesn’t have HGPRT enzyme 1. Fused plasma Present 2. Fused myeloma Absent 3. Hybridoma Present 4. Unfused plasma Present 5. Unfused myeloma Absent HGPRT
  • 11. 11
  • 12. 12 • ELISA screening method which done by incubating hybridoma culture in which secondary enzyme gets conjugate & formation of colored products shows positive hybridoma . • Used for multiplying the hybridoma cells :  In – vivo  In – vitro
  • 13. 13
  • 14. 14 Serological : • Identification of ABO blood group . Immunopurification : • Purification of individual interferon using monoclonal . • Inactivation of T - lymphocytes responsible for rejection of organ transplants. Therapy : • Removal of tumor cell from bone marrow. • Treatment of acute renal failure. • Treatment malignant leukemic cells , B cell lymphocytes , and a variety of allograft rejections after transplantation .
  • 15. 15