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BCG vaccine

The formulation of international requirements for the manufacture and control of BCG vaccine was first considered by the WHO Expert Committee on Biological Standardization in its thirteenth report. In its fourteenth report, the Committee requested WHO to make arrangements as soon as possible for the formulation of such requirements. These requirements were approved by the WHO Expert Committee on Biological Standardization at its eighteenth meeting and appeared as Annex 1 to its report.

Mycobacterium tuberculosis (Mtb), the ethiological agent of tuberculosis (TB), is a leading cause of human disease and death, particularly in developing countries. In the global context, TB in intimately linked to poverty, and control of TB is ultimately a question of justice and human rights. In some areas with a high burden of TB, existing strategies for TB control are currently overwhelmed by the rising numbers of cases of TB occurring in parallel with or the HIV/AIDS pandemic. Emerging mycobacterial drug resistance is further complicating the situation. After decades of steady decline, the incidence of TB is also increasing in industralized countries, mainly as the result of outbreaks in particularly vulnerable groups.

The bacille Calmette-Guérin (BCG) vaccine has existed for 80 years and is one of the most widely used of all current vaccines, reading >80%of neonates and infants in countries where it is part of the national childhood immunization programme. BCG vaccine has a documented protective effect against meningitis and disseminated TB in children. It does not prevent primary infection and, more importantly, does not prevent reactivation of latent pulmonary infection, the principal source of bacillary spread in the community. The impact of BCG vaccination on transmission of Mtb is therefore limited.

The biological interaction between Mtb and the human host is complex and only partially understood. Recent advances in areas such as mycobacterial immunology and genomics have stimulated research on numerous new experimental vaccines, but it is unlikely that any of these urgently need vaccines will be available for routine use within the next few years. In the meantime, optimal utilization of BCG is encouraged.

:: Background

:: The pathogen

RELATED DOCUMENTS

Technical report series
Including WHO guidelines and recommendations

Meeting reports

WHO vaccine position papers

HIGHLIGHTS

NEW ! For Public Comment by 9 October 2009
BS/09.2108-Recommendations to assure the quality, safety and efficacy of pneumococcal conjugate vaccines
Download [pdf 385kb]

NEW ! For Public Comment by 9 October 2009
BS/09.2109-Guidelines for Independent Lot Release of Vaccines by Regulatory Authorities
Download [pdf 222kb]

NEW ! For Public Comment by 9 October 2009
BS/09.2110-Guidelines on Evaluation of Similar Biotherapeutic Products (SBPs)
Download [pdf 279kb]

NEW! Request for Proposal - Submission of proposals by 28 September, 2009
Production of Sabin Poliovirus Master and Working Seeds to Ensure Future Production of both Live and Inactivated Polio Vaccines
Download [pdf 64kb]

Meeting Report-WHO Workshop in Training Performance of Potency Testing and Lot Release of Human Papillomavirus (HPV) Vaccines
NIBSC, UK, 11-15 May 2009
Download [pdf 136kb]

Further H1N1 specific update of TRS 941, Annex 5
Download [pdf 145kb]

H1N1 specific-update of TRS 941, Annex 5
Download [pdf 162kb]

ECBS 2008 Outcomes
Download [pdf 37kb]

Proposed Guidelines: Regulatory Preparedness for Human Pandemic Influenza Vaccines
Download [pdf 690kb]


UPCOMING EVENTS

WHO Informal Consultation on Standardization and Evaluation of BCG Vaccines
22-23 September 2009, Geneva, Switzerland

WHO Informal Consultation on Acellular pertussis vaccine and DTP based combined Vaccines
9-13 November 2009, Geneva, Switzerland