immunization

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Dr Ubaid N P JR Community Medicine, Pariyaram Medical College

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Dr Ubaid N P

JR Community Medicine,

Pariyaram Medical College

Specific defences :

Micro organism-breach local defense systems

host recognize, destroy and eliminate antigenic

material foreign to its own

Specific defenses are

1.Active immunity – humoral, cellular , combined immunity

2.Passive immunity – normal human Ig, specific human Ig, animal antitoxin or antisera

Active immunity

- Immunity developed as a result of infection or by specific immunization and is usually associated with the presence of Ab or cells having specific action on micro organism or its toxin. - Immunity produced is specific for particular diseases

Active immunity may be acquired by following :

-clinical infection

-sub clinical or in apparent infection

-immunization with an antigen

THE IMMUNE RESPONSEA. Primary response:

-Ag first time administer IgMAb -----IgGAb

-Nature and extend of primary response to an

Ag is determined by factors like

-Dose of Ag, nature of Ag, route of

administration, nutritional status of the host etc.

Following primary response RES is educated . There s production of memory cells by both B & T lymphocytes

These cells are responsible for immunological memory which become established after immunization

In fact purpose of immunization is to develop immunological memory.

B. Secondary (booster) response:

-secondary response involve production of both IgM &

IgG antibody

Response to booster dose differs in a no. of ways from primary response

(a) Production of Ab more rapid

(b) Ab response maintained at higher level for a long period of time

(c) Ab tends to have a greater capacity to bind to Ag

Humoral immunity It comes from B cells (bone marrow derived

lymphocytes) which proliferate and manufacture specific Ab after Ag presentation by macro phages

Immunoglobulin's are divided into 5 classes – IgG, M,A,D &E .

they circulate in body and neutralizes the microbes/toxins

Ab are specific- they react with same Ag when provided

Cellular immunity Some micro organism like M.Leprae , M.TB escape

humoral immunity and can multiply in macrophages . However these macrophages can be stimulated by T-lymphocytes.

The activated macrophages perform a much more efficient phagocytic function than non- activated macrophages

T cells do not secrete Ab , but they are responsible for recognition of Ag

Combination of both In some cases they jointly helps in immunity

Vaccine to be effective must ellicit both cell mediated and humoral responses

Active immunity takes time to develop . It is superior to passive immunity because

(a) duration of protection is long lasting

(b) With few exceptions severe reactions are rare

(c) Protective efficiency is better than passive

(d) Active is less expensive

Passive immunity Ab produced in one body ( human / animal ) are

transferred to another to induce protection against disease

That is, they are ready made Ab

Passive immunity may be induced by

(a) Ig or anti serum administration

(b) Ab through placenta , human milk (IgA)

Passive immunity differ from active immunity by

(a) Immunity is rapidly established

(b) Immunity produced is only temporary ( days to months ), till when Ab is eliminated from the body

(c) There is no education of RES

Herd immunity It is the level of resistance of a community or a group

of people to a particular disease

Eg: polio vaccine-------, chickgunya in Alappuzha

Elements contributing to herd immunity

(a) Occurrence of clinical or sub-clinical infection in herd

(b) Immunisation of the herd

(c) Herd structure

If herd immunity high enough , occurrence of epidemic is highly unlikely

Herd immunity is maintained by immunisation

Eg: polio , diphtheria

With no vaccine for small pox herd immunity is declined

Immunising agents Vaccines- substances-designed to produce specific protection

against a given disease It stimulate production of protective Ab(a) Live vaccine (attenuated )Prepared from live organisum . Doesn’t have the property of

phathogenicity but retained immunogenicity Should not be administered to immune deficient people,

pregnancyIf two live vaccine required – either given at two sites

simultaneously or with an interval of at least three weeksShould be properly storedUsually require only one dose , exception of polioEg: polio , BCG , measles , rubella

(b) Inactivated / killed vaccine

Virus is killed with heat or chemicals and infected into the body to stimulate active immunity

They are usually safe but less efficacious than live vaccines

Usually require more than two to three primary and even a booster dose to produce adequate Ab response

Usually administered i/m or s/c

Only severe C/I is severe local or general reaction to previous dose

Eg: pertusis , IPV, typhoid

Toxoid:

Exotoxins produced by certain organisum are detoxicated and used to prepare vaccines

These Ab produced neutralises the toxin moiety produced during infection and not the organism

Highly efficacious and safe

Eg : tetanus and diphtheria

Cellular fraction:

Prepared from extracted cellular fractions like cell wall, capsule etc

Efficacy and safety high

Eg : meningiococcal, pneumococcal

Combination:

Simplify administration, reduce cost, minimise no. of contact of patient with health system

Eg : DPT , MMR, Pentavalent

Polyvalent : prepared from two or more strains of same species . Eg : polio infuenza

Autogenous vaccine : organism in vaccine is obtained from the same patient

Vaccine can be plain , adjuvant , freeze dried preparation

Adjuvant is added to vaccine with an intent of potentiating the immune response.eg : aluminiumphosphate, aluminium hydroxide

Freeze dried vaccines ( BCG , Measles , YF) are more stable preparations than liquid vaccines

Immunoglobulin Composed of five major classes and its sub units-

IgG,M,D,A,E

Ig preparations : two types

(a) Normal human Ig

(b) Specific human Ig – usually made from plasma of patients who have recently recovered from infection

Live vaccine should not be given normally for 12 weeks after giving normal human Ig and if already given NHIg should be differed for 2 weeks

Eg : Hep A, Hep B, Tetanus, Rabies

Antisera and antitoxins They are materials prepared in animals ( horses)

Passive immunization is achieved

Eg: tetanus, snake bite, diphtheria

Cold chain It is the system of storage – transportation of vaccines

from the manufature to the actual vaccination site

Polio is most sensitive to heat among vaccines requires storage at -20 degree C.

Vaccine stored in freezer compartment are polio and measles

Vaccine in cold part but never allow to freeze are ‘T’ series vaccine, DPT, TT,DT,BCG & diluents

Vaccine should be protected from sunlight and anti septics

If refrigerated temperature is kept between 2 and 8 degree C vaccines (except polio) can be stored upto 5 weeks

Reconstituted BCG and measles are kept +2 to +8 degree C for max, of 4 hours and JE vaccine upto 2 hours

Return the unused vaccine vial to PHC from site on the same day in cold chain

Discard vaccine that are unused more than 3 times

Cold storage equipment(a)Walk-in cold room:

Located at regional level

meant to store up to 3 months

Serve 4 to 5 districts

(b) Deep freezer:

supplied to all districts (large) & PHC (small)

Cabinet temperature is -15 to -25 degree C

In case of power failures they can maintain cabinet temperature upto 18 to 22 hours

At PHC level deep freezer are used only for ice pack preparation and not for vaccine storage

( c) Ice lined refrigerator ( ILR):Kept at district ( large) and PHC (small)Cabinet temperature is maintained at +2 to +8At PHC, ILR are used to store vaccinesILR are lined with tubes or ice packs to maintain internal

temperatureILR can keep vaccine safe with 8 hours of continuous

electricity supplied in a 24 hour periodThey are top opening – can hold cold air inside better than

front openingVaccine kept in basket along with diluentsKeep spaces with boxes

A dial thermometer is kept in ILR and temperature is recorded twice a day

In case of electric supply failure or during defrosting vaccines transferred to cold boxes

DO’S - keep away from direct sunlight and 10 cm away from wall ,

keep voltage stabiliser,

keep equipment levelled ,

keep space between vaccines for air circulation,

open only when necessary, defrost periodically

DONT’S – Not to keep anyother equipments drugs ,food, water inside it

Discard expired vaccine

(d) Cold boxes :

Supplied to all peripheral centers

Used mainly for transportation of vaccines

Ice pack are placed at bottom and sides

Vials of DPT , DT , TT & diluents should not be placed in direct contact with frozen ice packs

(e) Vaccine carrier:Used to carry small quantities of vaccine ( 16 to 20 vials)4 frozen ice pack are used for lining the sides(f) Day carrier :Used to carry small quantity (6 to 8 vials)2 frozen ice packs are to be used Used only for few hours(g) Ice packs:Only water is filled upto the level markedIf leaking discarded

-risk of cold chain failure is greatest at sub-centre level. Hence , vaccines are not stored there.

Vaccine vial monitor(VVM)

Adverse events following immunization(AEFI)

(a) Vaccine reaction

(b) Programme error

(c) Coincidental

(d) Injection reaction

(e) Unknown

--precautions to be taken

Contra indications of vaccine

NIS- national immunization schedule

UIP – universal immunization programme – infancy

EPI – expanded programme on immunization – till 5 years

Pulse polio immunization

Catch up- keep up- follow up