4th Pediatric Infectious Diseases Conference
 
 
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Pedi Poll
Today's Poll
Should teicoplannin, colistin be used in case of neonatal sepsis where culture does not reveal any organism_?
No, it should be used only after drug sensitivity report
Yes, under guidance of an infectious disease expert
Newer Tuberculosis Vaccines
NEWER TUBERCULOUS VACCINES

LIMITATIONS OF BCG :-

  • Waning of protective immunity with time. Published data suggests that duration of protection is not more than 10 years.

  • Data from different studies indicates that BCG efficacy ranges from 0-80%.

  • Effectiveness is reduced in disseminated tuberculous disease.

  • Problem of a live vaccine in immunocompromised host.

  • Not protective against reactivation of tuberculosis or HIV associated Koch's.

There is therefore an urgent need for the development of more effective, better-standardized, affordable vaccine with durable activity and fewer side effects.

NEWER VACCINES BEING DEVELOED :-

  • Rationally attenuated Mycobacterium Tuberculosis.

  • Recombinant BCG.

    • Current TB vaccine strain mycobacterium bovis BCG endowed with a pose forming cytolysin.

    • V. Salmonella typhimurium secreting a single immunodominant antigen shared by BCG and mycobacterium tuberculosis.

  • Over expressing Mycobacterium Tuberculous Antigen.

  • Protein subunit vaccine

  • DNA Vaccines

Many of these vaccines have been tested for immunogenicity and protective efficacy in experimental animals. In addition alternate routes of tuberculosis vaccine delivery (e.g. oral, respiratory, gene gun) and various combinations of priming or boosting an experimental vaccine with BCG have been examined in relevant animal models.

BCG in SPECIAL SITUATIONS :-

  • BCG & LBW Infant : BCG vaccine and OPV administered in early neonatal life showed successful BCG reaction in 95.5% Infants.

  • One recent study from India suggested that BCG vaccination has an immunomodulatory role in case of IDDM & NIDDM.

  • BCG & Other Vaccines : Administration of BCG at the time of priming markedly increased the cellular & antibody responses to Hepatitis B & oral polio vaccine.

References :-

  1. McMurray DN. Recent progress in the development and testing of vaccines against human tuberculosis. Int J Parasitol. 2003;33(5-6):547-54
  2. Britton WJ, Palendira U. Improving vaccines against tuberculosis. Immunol Cell Biol. 2003 ;81(1):34-45.
  3. von Reyn CF, Vuola JM. New vaccines for the prevention of tuberculosis. Clin Infect Dis. 2002;35(4):465-74.
  4. Dhar N, Rao V, Tyagi AK. Recombinant BCG approach for development of vaccines: cloning and expression of immunodominant antigens of M. tuberculosis. FEMS Microbiol Lett. 2000;90(2):309-16.
  5. Kaur S, Faridi MM, Agarwal KN. BCG vaccination reaction in low birth weight infants. Indian J Med Res 2002;116:64-9.
  6. Sanjeevi CB,Das AK, Shtauvere-Brameus A. BCG vaccination and GAD65 and IA-2 autoantibodies in autoimmune diabetes in southern India. Ann N Y Acad Sci 2002 Apr;958:293-6.
  7. Horwitz MA, Harth G. New vaccine against tuberculosis affords greater survival after challenge than the current vaccine in the guinea pig model of pulmonary tuberculosis. Infect Immun 2003;71(4):1672-9.
  8. Wang J, Zganiacz A, Xing Z. Enhanced immunogenicity of BCG vaccine by using a viral-based GM-CSF transgene adjuvant formulation. Vaccine 2002;20(23-24):2887-98.
  9. Ota MO, Vekemans J, Schlegel-Haueter SE et al. Influence of Mycobacterium bovis bacillus Calmette-Guerin on antibody and cytokine responses to human neonatal vaccination. J Immunol 2002;168(2):919-25.
  10. Hess J; Kaufmann SH.Development of live recombinant vaccine candidates against tuberculosis. Scand J Infect Dis 2001;33(10):723-4
  11. Core information for the development of Immunization Policy. WHO- Vaccines and Biologicals. 2002 Update
Last Updated on 05-11-2004 Courtesy Pediatric Oncall

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