Immunization. - is the process by which an individual's immune system becomes fortified against an agent (known as the immunogen). immune systemimmunogen.

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Immunization. - is the process by which an individual's immune system becomes fortified against an agent (known as the immunogen). immune systemimmunogen

Immunization. The adaptive immune system:adaptive immune system When this system is exposed to molecules that are foreign to the body, it will orchestrate an immune response, and it will also develop the ability to quickly respond to a subsequent encounter (through immunological memory).molecules immunological memory

Immunization. The most important elements of the immune system that are improved by immunization are the B cells (and the antibodies they produce) and T cells. Memory B cell and memory T cells are responsible for a swift response to a second encounter with a foreign molecule.B cellsantibodiesT cellsMemory B cellmemory T cells

Vaccines. Immunization is done through various techniques, most commonly vaccination. Vaccination against microorganisms that cause diseases can prepare the body's immune system, thus helping to fight or prevent an infection.vaccination.microorganisms diseases infection

The immunization result in: – Anti toxin – Anti invasive – Neutralizing activity – Other types of protective humoral or cellular response in the recipient.

IMMUNITY & IMMUNIZATION II.Immunizations: A.Types: ● Active ● Passive

Active Immunization: Administration of all or part of a microorganism or a modified product of that microorganism i.e. a toxoid, a purified antigen, or an antigen produced by genetic engineering → to evoke an immunologic response(produce Antibody) mimicking that of the natural infection but that usually present little or no risk to the recipient. (Ag containing prepration).

what are the advantages of a live attenuated vaccine? -they act like the natural infection with regard to their effect on the immune response -Immunity develops slowly. -stimulates longer lasting antibody production -used for long term prophylaxis. -induce antibody production and resistance at the portal of entry for the natural virus

Active Immunization Types Live attenuated – VirusMeasles, mumps, rubella – BacteriaBCG Killed – VirusHepatitis B – Bacteria WholePertussis ToxoidTetanus PolysaccharideMeningoccocal

what is the advantage of using an inactivated vaccine? no chance of it reverting back to virulent form

Why we need booster doses? Inactivated and sub-unit(influenza) preparation are incapable of replicating in the host, these vaccines must contain a sufficient antigenic mass to stimulate the desired response maintenance of long-lasting immunity with inactivated viral or bacterial vaccines often requires periodic administration of booster doses.

what is the advantage of using an carrier protein or adjuvant? -Enhance APC receptors and cytokine release -carrier protein recruit helper T cells and induce IgG antibody responses -conjugate bacterial vaccines

what is a toxoid? a toxin produced by a bacterial organism that is inactivated by formalin Eleminated toxicity without eleminating immunogenicity.

Passive immunization is when antibodies are introduced directly into the body to give passive immunization. Produce immunity quickly. Used for short term prophylaxis and therapeutically. Temporary effect short acting.

Human Immune Serum Globulin Specific – IMHepatitis B (HBIG) Rabies (RIG) Tetanus (TIG) Varicella (VZIG) – IVCMV (CMV-IG) RSV (RSV-IG)

Passive Immunization (Cont) SPECIFIC EQUINE ANTIBODIES (IM) – BOTULISM ANTITOXIN – DIPHTERIA ANTITOXIN – TETANUS ANTITOXIN – SNAKE & SPIDER ANTI-VENOM MONOCLONAL ANTIBODIES (IV) – ANTI-ENDOTOXIN ANTIBODIES

Bacillus Calmette ‑ Guerin Vaccine (BCG). INDICATIONS – All tuberculin negative infants – Intradermal route PRECAUTIONS & CONTRAINDICATIONS(CI): – Give only to PPD negative children – CI in persons with immunodeficiencies – CI during pregnancy

Diphtheria, Tetanus & Pertussis (DTP) PREPARATIONS – < 7 years : DTP, DT if we give it alone there is an increased chance of side effect, DTaP (acellular pertussis vaccine) – > 7 years : Td, TdaP ( in adults risk of pertussis is very low so we don’t give its vaccination ) – (Td:adult tetanus toxoid full dose and diphtheria toxoid reduced dose) ADMINISTRATION – IM

Diphtheria, Tetanus & Pertussis (DTP) CONTRAINDICATIONS (CI) – Encephalopathy within 7 days – Progressive or unstable neurological disorders – Anaphylactic reaction to a previous dose PRECAUTIONS – severe systemic reactions such as Temp > C ( 1 st side effect) Must bring him to the ER if there was redness and pus discharge indicating cellulitis and the child shouldn’t take the other dose. persistent inconsolable crying > 3 hours Collapse episodes Convulsions

Measles, Mumps & Rubella (MMR) PREPARATIONS: – MEASLES. – MMR. ADMINISTRATION: – SC. INDICATIONS: – Primary immunization at 1 & 6 years – New recommendation : 3 doses at 12 m & 18 m & 6 years

Pneumococcal vaccine PREPARATIONS: – Purified capsular polysaccharide of 23 serotypes of Streptococcus pneumoniae – 13 valent conjugated vaccine ADMINISTRATION: – IM / SC – 3 primary dose + 1 booster

Pneumococcal vaccine INDICATIONS: – Primary vaccination (conjugate vaccine) – children 2 yr. or older with Anatomical or functional asplenia Sickle cell disease Nephrotic syndrome Immunosuppression Note:any child less than 2 years is given the conjugated form with the carrier protein so body will get immunized by T cells. Child greater than 2 years is given the capsular polysacharride form

Meningococcal vaccine PREPARATIONS: – monovalent (A or C) – bivalent (A & C ) – quadrivalent (A,C,Y & W ‑ 135) – quadrivalent conjugate quadrivalent ADMINISTRATION: – SC – Given at age of 9&12 months

Meningococcal Prophylaxis INDICATIONS: – Control of outbreaks – Children with complement deficiencies or asplenia SIDE EFFECTS: – local erythema and discomfort – transient fever

VACCINES AVAILABLE FOR ACTIVE IMMUNIZATION RouteTypeVaccine Intradermal (Preferred) or subcutaneous Live bacteria BCG Subcutaneous intramuscular or intradermal Inactivated bacteria Cholera Intramuscular Toxoids and inactivated bacteria DTP

VACCINES AVAILABLE FOR ACTIVE IMMUNIZATION (cont) RouteTypeVaccine Subcutaneous Live virus Rubella IntramuscularToxoids Tetanus & TD, DT Subcutaneous (Boosters may be intradermal) Inactivated bacteria Typhoid Subcutaneous Live virus Yellow fever

VACCINES AVAILABLE FOR ACTIVE IMMUNIZATION (cont) RouteTypeVaccine Subcutaneous Live viruses MMR Subcutaneous Live virus Mumps Oral OPV Intramuscular Inactivated bacteria Plague Intramuscular or subcutaneous PolysaccharidePneumococcal Intramuscular Inactivated virus Rabies

VACCINES AVAILABLE FOR ACTIVE IMMUNIZATION (cont) RouteTypeVaccine Intramuscular Inactivated viral antigen Hep. B Subcutaneous intramuscular Polysaccharide Haemop. B Intramuscular (Preferred) or subcutaneous Inactivated virus Influenza Subcutaneous IPV Subcutaneous Live virus Measles SubcutaneousPolysaccharideMeningococcal

MMR, OPV and yellow fever are the only live virus vaccines. BCG is the only live bacterial vaccine.

ROUTINE ACTIVE IMMUNIZATION FOR INFANTS & CHILDREN VaccineAge BCG, HBV 1 st At birth DPT + HiB + OPV 1 st, HBV 2 nd 2 months DPT + HiB + OPV 2 nd 4 months DPT + HiB + OPV 3 rd, HBV 3 rd 6 months MMR 1 st 12 months DPT + HiB + OPV 1 st booster 18 months DPT + OPV 2 nd booster, MMR 2 nd 4 – 6 years Td (Repeated every 10 yrs.) 14 – 16 years

Revised Basic Vaccination Schedule اللقاحVaccineAge الدرن ، الالتهاب الكبدي (ب) BCG, HepB At birth شلل الاطفال المحلل ( الثلاثي البكتيري،الالتهاب +الكبدي ب، المستديمة النزلية) IPV (DTaP, HepB, Hib)+PCV+rota 2 months شلل الأطفال المحلل(الثلاثي البكتيري، الالتهاب الكبدي ب، المستديمة النزلية) IPV (DTaP, HepB, Hib)+PCV+rota 4 months شلل الاطفال الفموي OPV (DTaP, HepB, Hib)+PCV 6 months الحصبة المفرد (Mono)+ Measles (Mono)+meningococcal conjugate quadrivalent 9 months شلل الاطفال الفموي، الثلاثي الفيروسي، الجديري المائي + OPV, MMR, +PCV+meningococcal conjugate quadrivalent 12 months شلل الاطفال الفموي (الثلاثي البكتيري،المستديمة النزلية) ، الالتهاب الكبدي(أ) OPV (DTaP, Hib),MMR, Varicella+ HepA 18 months الالتهاب الكبدي(أ) HepA 24 months شلل الأطفال، الثلاثي البكتيري، الثلاثي الفيروسي، الجديري المائي OPV, DTaP, MMR, Varicella 4 – 6 Years

Catch up (for those who missed it) schedule < 7 yr. First visit :Dtab,Hib,HBV,MMR,PCV Interval after first visit 1 mo :DTaP,IPV,HBV,Var.PCV 2 mo:DTaP,Hib,IPV.PCV >8 mo:DTaP,HBV,IPV.PCV

Catch up schedule > 7 yr. CommentsRecommended Vaccine (s) Before giving BCG, Tuberculin, skin testing is recommended if feasible. BCG, Td, OPV1 st visit Interval after 1 st visit MMR1 month Td, OPV2 months Td, OPV8 – 14 months Repeat every 10 yrs. throughout life Td10 years

Catch up immunization schedule for aged 4 m through 6 yrs who start late or who are more than one month behind. Dose 4 to dose 5 Dose 3 to dose 4 Dose 2 To dose 3 Interval Dose 1 to dose 2 minimum.a age for dose 1 vaccine 8 weeks4 weeksBirthHepatitis 6 m if the 4 th dose given <4 yrs 6 months 4 weeks 6 weeksDiphtheria, tetanus, pertussis, 8 w if 3 doses<1 2m 4 w if <12m 8 w if >12m 0 15m 4 w if age <12m 8 w if >12m 0 15m 6 weeksHIB 8 if 3 m 4 if <12m 8 0 4w if <12m 8w or >12m 0 m 6 weekspneumococcal

Catch up immunization schedule for aged 4 m through 6 yrs who start late or who are more than one month behind. Dose 3- 4 Dose 2-3Dose 1-2Minimum age for dose 1 Vaccine 4 w 6 wInactiva Polio 4 w12 mMMR 3 m12 mVaricella 6 m12 mHepatitis A

Catch up immunization schedule for aged 6 yrs through 18 years. Dose 4 to dose 5 Dose 3 to dose 4 Dose 2 To dose 3 Interval Dose 1 to dose 2 minimum. age for dose 1 vaccine 8 weeks4 weeksBirthHepatitis B 6 months if 1 st dose <12 m.of age 4 weeks if 1 st dose <12m. 6 months if 1 st m or >. 4 weeks7 yrsTetanus,Diphtheria /Tetanus Diphtheria, pertussis (Td),(Tdap) 4 w 6 weeksInactivated Poliovirus 3 m if <13yrs 12 mVaricella 6 m12 mHepatitis A 4w12mMeasles,Mumps,Rubella.

Complications &contraindications. - Swelling, discomfort at the injection site and mild fever. -If there is family hx of febrile convulsion, advice on fever prevention should be given. After vaccination, it’s advisable to give the child paracetamol cause its an anti-pyretic and analgesic

Complications &contraindications Live vaccine should not be given to children with impaired immune responsiveness (except in children with HIV infection in whom MMR vaccine can be given if HIV was under control ).

Complications &contraindications Moderate or severe illness with or without fever ( mild infection without fever are not a contraindication ) Anaphylactic reaction to vaccine or vaccine constituent Pregnant women Immunocompromised / Immunosuppressed children shouldn’t take Live attenuated vaccines as BCG Within months of immunoglobulin administration in treating ITP patients because antibodies will atack the immunoglobulins.

- Complications &contraindications The only contraindication to pertussis vaccination if the child has experienced a sever local or general reaction to a preceding dose. -If there is an evolving neurological problem, immunization should be deferred until the condition is stable.

Immunization Of Special Groups IMMUNOCOMPROMISED HOSTS Avoid MMR, measles (may be used in HIV) Avoid OPV; use IPV for these children and their household contacts (gastrointestinal excretions of po vaccine). PRETERM INFANTS Treat as term babies Avoid OPV in hospital Influenza vaccine in BPD (bronchopulmonary dysplasia) may delay HBV if <2 kg & mother is HBsAG negative

What is the benefit of the Live attenuated polio oral vaccine? is it still used today? -provides local and systemic immunity - It is discontinued in the U.S because of the risk of developing paralytic poliomyelitis in those immunecompromised. It is still used in other parts of the world While IPV provides only local immunity.

Influenza Virus Nature of vaccine: – Killed vaccine(injection). – Live attenuated(intranasal) Preparations: – whole and “split virus” vaccines. – “split virus” vaccines are recommended for children 6 months and older. – composition of the vaccine is changed annually.

Influenza vaccine. Indications: – Sickle cell anemia. – Chronic salicylate therapy. – Diabetes mellitus. – Chronic renal disease. – Chronic metabolic disease. – immunosuppressive conditions: cancer, HIV etc. – Hospital personnel with significant patient contact.

Immunization & Immunity Misconceptions concerning vaccine contraindications Mild acute illness with low-grade fever or mild diarrhea illness in an otherwise well child. Current antimicrobial therapy or the convalescent phase of illness.