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ACTIVE AND PASSIVE
IMMUNITY
• A person said to be immune when he possesses “specific
protective antibodies or cellular immunity as a result of
previous infection or immunization”.
• Specific defences
1. Active immunity :- (a) Humoral immunity
(b) Cellular immunity
(c) Combination of the above
2. Passive immunity :- (a) Normal Human Ig
(b) Specific Human Ig
(c) Animal antitoxin and
antisera
ACTIVE IMMUNITY
• An individuals develops as a result of infection or by
specific immunizations
• Associated with presence of antibodies or cells
having a specific action on microorganism concerned
with a particular infectious disease or on its toxin.
• Depends upon the humoral and cellular response of
the host.
• Specific for a particular disease.
• Acquired in 3 ways:
(a) Following clinical infection – chickenpox, measles
and rubella
(b) Following subclinical infection- polio and diphtheria
(c) Following immunization with an antigen (vaccine)
- Live attenuated vaccine, killed vaccine and toxoid
IMMUNE RESPONE
A. PRIMARY RESPONSE
• When an antigen is administered for the first time
to an animal or human, there is latent period of
induction of 3-10 days before antibodies appear In
the blood.
• Antibody, elicited first is entirely of the IgM type.
• IgM antibody titer rises steadily during the next 2-3
days, reaches a peak level and then declines almost
as fast as it developed.
• If the antigenic stimulus was sufficient, IgG appears
in few days, reaches in peak in 7-10 days and then
gradually falls over a period of weeks or months.
- Nature and extent of primary response is determined
by number of factors:
• Dose of antigen
• Nature of antigen
• Route of administration
• Adjuvants
• Presence of maternal antibody
• Nutritional status of the host
• Genetic and co-existing diseases
• An important outcome of primary antigenic
challenge is education of reticuloendothelium system
of the body.
• Production of memory cells or primed cells by both B
and T lymphocytes.
• These cells are responsible for immunological
memory
B. SECONDARY (BOOSTER) RESPONSE
• Differs in a number of ways from the primary
response:
- Shorter latent period
- Production of antibody more rapid
- Antibody more abundant
- Antibody response maintained at higher levels for
a longer period of time
- Antibody have greater capacity to bind to the
antigen
1. HUMORAL IMMUNITY
• Comes from the B-cells (bone marrow derived
lymphocytes) which proliferate and manufacture
specific antibodies after antigen presentation by
macrophages.
• Antibodies circulate in the body and act directly by
neutralizing the microbe or its toxin.
• Antibodies are specific, they react with same antigen
which provoked their production.
• It will not provide protection against more than one
antigen.
2. CELLULAR IMMUNITY
• Some pathogen (M. leprae, M. tuberculosis, S. typhi)
escape the bactericidal action of leukocyte.
• Stimulation of macrophages by specific stimulated T-
lymphocytes (thymus derived lymphocytes).
• Activated macrophages perform a much more
efficient phagocytic action.
• T- cell do not secrete antibody but are recognition
for antigen.
• On contact with antigen, the T-cells initiate a chain of
responses:
- Activation of macrophages
- Release of cytotoxic factors
- Mononuclear inflammatory reactions
- Delayed hypersensitivity reactions
- Secretions of immunological mediators
• Responsible for immunity against many diseases like
TB, brucellosis etc.
3. COMBINATION OF THE BOTH
• B and T lymphoid cells, both cooperate with one
another and with certain accessory cells such as
macrophages and human K (killer) cells, and their
joint functions constitute the complex events of
immunity.
PASSIVE IMMUNITY
• When antibodies produced in one body (human or
animal) are transfer to another to induce protection
against disease.
• Body does not produce its own antibodies, depends
upon ready-made antibodies.
• Passive immunity may be induced by:
- Administration of an antibody-containing
preparation (immune globulin or antiserum)
- Transfer of maternal antibodies across the placenta
- Transfer of lymphocytes, to induce passive cellular
immunity
• Passive immunity differs from active immunity in the
following respects:
- Immunity is rapidly established
- Immunity produced is only temporary (days to
month)
- No education of the reticuloendothelial system
• Active immunity is superior to passive immunity
because:
- Duration of protection is long lasting
- Severe reactions are rare
- Protective efficacy is more
- Active immunization is less expensive

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Active and passive immunity

  • 2. • A person said to be immune when he possesses “specific protective antibodies or cellular immunity as a result of previous infection or immunization”. • Specific defences 1. Active immunity :- (a) Humoral immunity (b) Cellular immunity (c) Combination of the above 2. Passive immunity :- (a) Normal Human Ig (b) Specific Human Ig (c) Animal antitoxin and antisera
  • 3. ACTIVE IMMUNITY • An individuals develops as a result of infection or by specific immunizations • Associated with presence of antibodies or cells having a specific action on microorganism concerned with a particular infectious disease or on its toxin. • Depends upon the humoral and cellular response of the host. • Specific for a particular disease.
  • 4. • Acquired in 3 ways: (a) Following clinical infection – chickenpox, measles and rubella (b) Following subclinical infection- polio and diphtheria (c) Following immunization with an antigen (vaccine) - Live attenuated vaccine, killed vaccine and toxoid
  • 5. IMMUNE RESPONE A. PRIMARY RESPONSE • When an antigen is administered for the first time to an animal or human, there is latent period of induction of 3-10 days before antibodies appear In the blood. • Antibody, elicited first is entirely of the IgM type. • IgM antibody titer rises steadily during the next 2-3 days, reaches a peak level and then declines almost as fast as it developed. • If the antigenic stimulus was sufficient, IgG appears in few days, reaches in peak in 7-10 days and then gradually falls over a period of weeks or months.
  • 6. - Nature and extent of primary response is determined by number of factors: • Dose of antigen • Nature of antigen • Route of administration • Adjuvants • Presence of maternal antibody • Nutritional status of the host • Genetic and co-existing diseases
  • 7. • An important outcome of primary antigenic challenge is education of reticuloendothelium system of the body. • Production of memory cells or primed cells by both B and T lymphocytes. • These cells are responsible for immunological memory
  • 8. B. SECONDARY (BOOSTER) RESPONSE • Differs in a number of ways from the primary response: - Shorter latent period - Production of antibody more rapid - Antibody more abundant - Antibody response maintained at higher levels for a longer period of time - Antibody have greater capacity to bind to the antigen
  • 9. 1. HUMORAL IMMUNITY • Comes from the B-cells (bone marrow derived lymphocytes) which proliferate and manufacture specific antibodies after antigen presentation by macrophages. • Antibodies circulate in the body and act directly by neutralizing the microbe or its toxin. • Antibodies are specific, they react with same antigen which provoked their production. • It will not provide protection against more than one antigen.
  • 10. 2. CELLULAR IMMUNITY • Some pathogen (M. leprae, M. tuberculosis, S. typhi) escape the bactericidal action of leukocyte. • Stimulation of macrophages by specific stimulated T- lymphocytes (thymus derived lymphocytes). • Activated macrophages perform a much more efficient phagocytic action. • T- cell do not secrete antibody but are recognition for antigen.
  • 11. • On contact with antigen, the T-cells initiate a chain of responses: - Activation of macrophages - Release of cytotoxic factors - Mononuclear inflammatory reactions - Delayed hypersensitivity reactions - Secretions of immunological mediators • Responsible for immunity against many diseases like TB, brucellosis etc.
  • 12. 3. COMBINATION OF THE BOTH • B and T lymphoid cells, both cooperate with one another and with certain accessory cells such as macrophages and human K (killer) cells, and their joint functions constitute the complex events of immunity.
  • 13. PASSIVE IMMUNITY • When antibodies produced in one body (human or animal) are transfer to another to induce protection against disease. • Body does not produce its own antibodies, depends upon ready-made antibodies. • Passive immunity may be induced by: - Administration of an antibody-containing preparation (immune globulin or antiserum) - Transfer of maternal antibodies across the placenta - Transfer of lymphocytes, to induce passive cellular immunity
  • 14. • Passive immunity differs from active immunity in the following respects: - Immunity is rapidly established - Immunity produced is only temporary (days to month) - No education of the reticuloendothelial system
  • 15. • Active immunity is superior to passive immunity because: - Duration of protection is long lasting - Severe reactions are rare - Protective efficacy is more - Active immunization is less expensive