Types of Vaccines



What is Vaccine?

It is suspension of microorganism or fraction of microorganism which is used to induce immunity. The vaccine mimics the role of pathogen to the body. We might use a whole organism or part of it or sometime genetically engineered antigenic part to be injected or taken orally to produce immune response. As the microorganisms are virulent we need to make them avirulent. Here comes the difference how we make that organism avirulent which gives rise to different

Types of Vaccines

1.Conventional Vaccines
             a. Live attenuated (Live organism, but lacking the pathogenic part)

             These contain whole living pathogenic organisms. But those organisms are weakened; their pathogenic part is attenuated or removed. So they cannot cause the infection rather they mimic the actual infection to immune system. And body immune system produce antibodies show humoral and cell mediated response against them and become immune against that particular pathogenic organism.

Preparation of this vaccine, a virulent form of wild organism is taken usually a virus or bacteria, and placed in the differential media to subside its pathogenecity and make it a virulent. This is done by serial passage in foreign host like tissue embryonic egg or sometimes animals for multiple generations. So in this way mutations are introduced in the new host. The pathogen which is mutated now become different from the original virulent form and cannot cause the infection in the host but rather can induce an immune response. Sometimes high temperature conditions are also used to make microorganism attenuated. Live attenuated vaccines are prepared from the strains attenuated, which are completely devoid of pathogenecity but can induce immune response. They multiply in the human body and reside there for longer period of time.

Characters: Induce both Humoral and cell mediated immune response local and systematic. These are heat unstable. It has of reverting back to pathogenic form but very rare. So potential harm to individuals with compromised immunity. It gives sufficient time for memory cells production.

Applications: This technology is used to prepare vaccines for, Cholera (caused by G.Negative bacteria), Vaccines against Salmonella species, Tuberculosis BCG vaccines, Oral Polio Vaccine, Measles Vaccines, Leishmania Species Vaccine, Influenza Virus vaccines, Mumps and Rubella Vaccines.
               

 b. Inactivated Killed Vaccines (Killed microorganisms suspension)

             These also contain the whole organisms i.e. whole bacteria or virus suspension, but those are completely heat killed or inactivated. The organisms are pathogenic when killed they cannot cause any infection, when injected the body immune system recognize them as antigens and produce immune response against them. Thus body becomes immune against that particular type of organisms. 
Preparation: We take pathogenic organisms, and kill them through phenol or formalin. Earlier heat was also used, but there was a risk heat may not completely kill those microorganisms. Now a day’s Gamma Radiations are also used and proved more effective in killing those pathogenic organisms.

Characters: These do not stimulate local immunity. They produce shorter response thus required a booster injection. They do not produce cytotoxic T-cell response, as the pathogens are killed so safe in immune compromised individual too. Usually it is heat stable. These do not converted back to pathogenic or virulent form.

Application: Tab Vaccine against enteric fever, Polio vaccine and Influenza Vaccine, Typhoid Vaccine, cholera Vaccine, Also used against Rabies in humans, Pneumonia Vaccines.

                2. Genetically Engineered Vaccines

                                       These vaccines are prepared by genetic modification or just taken up the antigenic genes and them amplify them and then make GMOs.

                a. Subunit/Recombinant Vaccine

                 These only include the part of organism instead of using whole organism. The part is antigenic, which induce the immune response and results in the production of antibodies against that particular type of antigen used. The antigen part is protein, usually 1-20 antigens used at a time which are taken directly or cultured in the media taken from DNA of the Virus. These are also called recombinant DNA subunit vaccines.

Preparation: One method is, a protein is isolated from virus and administered, but thus protein may be weak and can be denatured and might associate with undesired antibody. Second method is recombinant vaccine, in which a antigen gene from Virus DNA is isolated and put into a vector which many be attenuated virus or bacterium. The GM vector will express the antigen and is of no risk to host. Bactria, viral, mammalian, yeast cells may be used for expression.

Characters: these may be single antigen or recombinant, Induce both humoral and cell mediated response, usually stable, can also be given to the immune compromised individuals; these are rather cheaper & simple to produce. Smaller quantities are required for immune response.

Applications: Influenza A and B vaccine, Recombinant Hepatitis B vaccine, Production of hybrid Virus Vaccines, HBsAg, and Rabies. It also used to develop vaccines for HIV and Ebola Virus.

                b. DNA Vaccine

            These are the newest and most promising vaccines. Usually a piece of DNA of Bacterial cell which is circular and small part. Experiments shows that plasmids with naked DNA inserted into the muscle results in the production of protein antigen (pathogen) encoded in the DNA. These proteins foreign to the host and result in the immune response. There are different DNA vaccines depending upon the host and vector being used. When the vectors used are highly expression ones, then the immune response elicits by the vaccine would be the best. Protein expression can be enhanced by optimizing the codons usage of pathogenic mRNA for eukaryotic cell. Altering the genetic sequence of immunogen to reflect the codon.

Preparation: First of all the vectors and the genes are cut with restriction enzymes at known sites, trimming of the open vectors and gene for gene ligation, the spliced gene is put in the vector and ends of the vectors joined with sliced gene. Now inserted into bacteria to get many copies of this recombinant gene. Now purify the altered vectors from the bacteria. Can be done by rupturing the bacterial cell and free vectors are obtained, now fill up the syringe with the altered DNA vectors and billions of the vectors inserted in the body and only 1% will work. Once the expressed proteins by these recombinant vectors leave the cell body will recognize them. 

Characters: These are safe with no side effects, inexpensive and easy to prepare, development time is relatively shorter, gives long term antigenic protein production thus require low boosters. It gives Cytotoxic T cell and helper T-cell response. And also Humoral response. Extended expression gives good long-term immunological memory. It is very stable DNA vaccine. It is not possible to revert back.

Applications: So far for humans there is still clinical trials are going on for usefulness. In animals two DNA vaccines are approved one is for horses protect them against West Neil Virus and other protects the salmon from viral disease.

               c. RNA Vaccine

   It involves the use mRNA for the synthesis of antigenic proteins instead of DNA genes. As the RNA is single stranded and different from DNA so there will be no chromosomal integration of foreign genetic material. When administered it will be translated to proteins and will trigger the immune response. RNA vaccines include mRNA and self amplifying RNA replicon has the ability to overcome limitation with DNA vaccine. RNA vaccines will be translated directly into the host cytoplasm. Work is still underway for the RNA vaccines to be available for Vaccination. These will work faster than DNA vaccines.

Preparation: mRNA can be synthesized invitro, which will be translated into the antigenic protein directly.

Characters: Economical and fast acting can induce Humoral and Cell mediated response. Can be given to immuno-compromised individuals. Long lasting and booster are required.

Applications: Can work quit well and efficiently where the DNA vaccines work. Still trial work undergo in cancer patients and HBV and HIV patients. Soon will be available in the market.

Mechanism of Vaccines against Infectious Diseases

Vaccines mimic the pathogen and trigger the humoral and Cell mediated immune response in the body. Vaccines contains the antigens whether the whole organism or antigenic part. DNA or RNA vaccines synthesis the antigenic part into the host. Thus these antigenic proteins detected by the immune system causes the immune response which include following main steps.

Antigens Sound The Alarm:

The molecule on the surface of microbes also called epitopes, taken as antigens. Every microorganism has unique set of epitopes and it is central to develop vaccines. Macrophages engulf the cells and carry the epitopes to the lymph nodes. A molecule called MHC displays these antigens to other immune cells. This presentation recognized by the T cells which trigger the B cells to produce antibodies.

Lymphocyte Takeover:

Now it’s time for lymphocytes which are B cells and T cells. T cells which are defensive, they secrete the chemicals to show defensive response. In this way some other immune responses may become activated. Helper T cells work with killer T cells and also help B cells. B cells are very important to make and secrete antibodies.

Except there are Cytotoxic T cells.CD8+ T lymphocytes which limits the infection. Also secrete antiviral Cytokines CD4+ T helper lymphocytes. These helper T cells may produce chemicals or help the B cells. Moreover CD4+ T cells are needed for the antibodies production.

Antibodies in Action:

Immune system only gets hold of antigens of the helper T cells and antibodies kill the organism at faster rate than their reproduction. And gradually the antigens or the microorganisms disappeared. After the eliminating the microbes or antigenic protein some of the T and B cells become the Memory cells and they quickly divide to make more antibodies against specific antigen for which they were given task. Memory T cells further grow and divide to become army of the immune system. Now when ever these particular type organisms will attack body this army will eliminate the infection.

 

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