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Vaccines (2)

May 29, 2018

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    M.S RAMAIAH COLLEGE OF ARTS, SCIENCE AND

    COMMERCE

    A SEMINAR REPORT ON

    SUBMITTED ON THE FULFILLMENT OF 1STYEAR M.SC 2ND SEM

    BIOTECHNOLOGY PRESCRIBED BY BANGALORE UNIVERSITY

    SUBMITTED BY: GUIDED BY:

    NAHID JAHAN ANSARI MRS. YASHODHA

    2ND SEM M.SC. BIOTECHNOLOGY DEPARTMENT OF BIOTECHNOLOGY

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    ACKNOWLEDGEMENT

    The submission of this seminar report gives me an opportunity to express

    my gratitude to all those inspiring forces, which have been the pillars

    behind the successful completion of this seminar.

    First of all I would like to thank Mrs Yashodha , Department ofBiotechnology for guiding me and helping me in the delivery of my

    seminar.

    I am also thankful to Mrs. Asha, Head of Department of

    Biotechnology for giving me the opportunity to deliver my seminar.

    Paramita Saha

    M.Sc Biotechnology

    IInd Semester

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    V

    ACCINES

    Submitted by:

    PARAMITA SAHA

    M.Sc BIOTECHNOLOGY

    II SEMESTER

    1

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    INDEX

    INTRODUTION03

    PRINCIPLE OF VACCINES

    04

    VACCINETION: A Bit Histoy

    05

    CLASSIFICATION06-08

    VACCINE CONTENTS

    09

    VACCINES PRODUCTION

    10

    CONVENTIONAL VACCINES

    11-12

    SUBUNIT VACCINES

    13-17

    SUMMURY

    18

    BIBLIOGRAPHY

    19 2

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    OVERVIEW OF THE PRESENTATION

    INTRODUTION

    PRINCIPLE OF VACCINES

    VACCINETION- A Bit Histoy

    CLASSIFICATION

    VACCINE CONTENTS

    VACCINES PRODUCTION

    CONVENTIONALVACCINES

    SUBUNIT VACCINES

    CONCLUSION BIBLIOGRAPHY

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    INTRODUCTION: What are vaccines?

    Injections or oral drops.

    Given any persons or even animals.

    To prevent any disease caused by virus or becteria.

    The word vaccine is derived from the Latin word vacca.

    In Latin vaccameans cow.

    First vaccines produced used the cowpox viruses from cow pox diseased

    cows. Hence the name.

    3

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    THE PRINCIPLE

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    PRINCIPLE OF VACCINATION

    When the same virus either weakened or killed are introduced

    intentionally into ones body.

    Virus or bacteria attacks can cause disease to a person.

    The body produces antibodies to fight against the virus.

    If the virus or bacteria attack such person , the antibodies which are

    already produced, fight against the disease, and the person is protected

    against the disease.

    Hence there is a resistence to the disease caused by the virus.

    Hence vaccines can be used to prevent diseases caused by viruses or

    bacteria.

    4

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    VACCINATION: A BIT OF HISTORY

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    HISTORY

    In 1978, Edward Janner, for the first time produced vaccines to

    induces resistence to small pox .

    Janner considered to be the founder of the system of vaccination.

    5

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    EDWARD JANNER

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    AN IDEAL VACCINE

    1. Should not be toxic or pathogenic.

    2. Should have very low level of side-effects

    3. Should not cause problems in individuals with an impaired immune system.

    4. Should not spread either within the vaccinated individuals or to the others

    individuals.

    5. Should not contaminant the environment.

    6. Should be effective in producing long lasting humoral and cellular

    immunities.

    6

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    7. The technique of vaccination should be simple.

    8. Should be cheap.

    7

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    CLASSIFICATION

    Two Types :

    1. Dead virus vaccines

    2. Live virus vaccines

    In dead virus vaccines, the viruses are killed.

    In live virus vaccines , the viruses are weakened.

    8

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    CONTENT OF VACCINES

    Vaccines- oil coloured/colourless clear fluid.

    It is made up of Virus

    About 7 million viruses are required for a dose of vaccination.

    If we make sauce out of tomato, called as tomato sauce.

    Vaccines are also similar to sauce but made up of viruses, hence knownas virus sauce.

    9

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    VACCINE PRODUCTION

    1. Production of viruses in huge numbers.

    2. Seperation of viruses.

    3. Weakening or killing of viruses.

    4. Proccessing, applying preservatives.

    5. Packing and dispatching

    10

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    CONVENTIONAL VACCINES

    It consist of whole pathogenic organisms, which may either be killed or

    live; the virulence of pathogens is greately reduced (attenuation).

    Conventional vaccines are produced in either whole animals or cultured

    animal cells.

    They are highly effective and relatively easy to produce at low cost.

    11

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    LIMITATION

    Safety: Reversion to virulence.

    Incomplete inactivation.

    Contaminations.

    Secondary effects: inflammation.

    Fever.

    Hypersensitivity

    Immunosuppression.

    Cold chain: refrigeration.

    Not available against all diseases: ASF Non-differentiation between vaccinated and sick animals.

    12

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    SUBUNIT VACCINES

    A vaccine containing viral antigens made free of viral nucleic acid by

    chemical extraction and containing only minimal amounts of nonviral

    antigens derived from the culture medium.

    It is less likely to cause adverse reactions than a vaccine containingthe whole virion.

    13

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    Advantages:

    Defined Composition

    Various delivery systems available

    Disadvantages:

    Antigens must be produced and purified by cultivation of a pathogen

    Multiple doses typically required

    Adjuvant needed

    14

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    RECOMBINANT SUBUNIT VACCINES

    Identify and isolate a specific gene from virulent bacteria or virusgene that codes immuno protective protein.

    Gene is inserted into plasmid DNA and ligated with ligase.

    New (engineered) plasmid inserted into another bacterium (transform).

    Allowed to grow and actually produce the antigenic protein.

    The vaccine is comprised of purified proteins recovered from theexpression vector.

    15

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    STRATEGIES OF R. SUBUNIT VACCINES

    1.Integration of the transgene into plant genome

    2.Expression as a coat protein fusion of a plant virus

    16

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    EFFECTIVENESS OF VACCINES

    Induce the right sort of immunity

    Be stable on storage

    Have sufficient immunogenicity

    17

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    SUMMARY

    1. A state of immunity can be induced by passive or active.

    2. In developing vaccine, the developing vaccine the branch of immune

    system to be activated must be considered.

    3. To induce immune system epitope must be present.

    4. To induce CMI, a vaccine capable of transient intracellular growth isdesirable.

    5. MHC class I molecule necessary for the CMI.

    6. Three types of vaccines are currently used in humans: Attenuated,

    inactivated, or Purified vaccines.

    7. Recombinant vectors , including vaccinia virus,canarypox&attenuted canbe carry multiple gene s from infectious mos .

    8. Plasmid DNA encoding a protein Ag from a pathogen has been shown

    effective vaccine.

    18

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    BIBLIOGRAPHY

    www.wikipedia.org

    www.britanica.com

    Immunology By: Kuby

    Immunology and Medical Microbiology By

    B.D Singh.

    19