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New Vaccine Development: Establishing Priorities: Volume II, Diseases of Importance in Developing Countries (1986)
Board on Population Health and Public Health Practice (BPH)

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. "Appendix D-18: The Prospects for Immunizing Against Vibrio cholerae." New Vaccine Development: Establishing Priorities: Volume II, Diseases of Importance in Developing Countries. Washington, DC: The National Academies Press, 1986.

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New Vaccine Development: Establishing Priorities, Volume II, Diseases of Importance in Developing Countries

DISTRIBUTION OF DISEASE

Geographic Distribution

Cholera has swept the world in seven great pandemic waves. From the early 1900s to 1961, cholera was virtually restricted to its endemic focus in the Indo-Pakistani subcontinent. The present pandemic, caused by V. cholerae of the El Tor biotype, began in 1958 in the Celebes Islands, Indonesia. It subsequently swept through and became endemic in the Philippines, Southeast Asia, and Africa. Outbreaks that have been more or less self-limited have occurred in the Soviet Union, Japan, Italy, Spain, northern Europe, and North America (including the United States). Cholera vibrios of the classical biotype appear to be reemerging in India and Bangladesh.

Disease Burden Estimates

The burden of disease caused by V. cholerae has been calculated only for areas in Africa and Asia where cholera is endemic. Table D-18.1 shows the estimated number of cases of the disease in Asia; Table D-18.2 presents the same information for Africa. The combined endemic disease burden for the two continents is shown in Table D-18.3.

No attempt has been made to estimate the disease burden produced by cholera epidemics or pandemics because it is very difficult to predict where and to what extent they will occur. This inability to identify a vaccine target population prevents calculation of potential health benefits that could be obtained from a vaccine. However, any vaccine developed to prevent endemic cholera could play a major role in curtailing epidemic cholera.

Traditionally, it has been assumed that cholera does not have any long-term sequelae. A recent epidemiological study in India suggests, however, that a strong association may exist between cataract development and episodes of cholera and other severe diarrheal diseases (Minassian et al., 1984). Because of the preliminary nature of this evidence, the committee chose not to include visual disability in the current disease burden estimates for cholera. Further research on this topic is warranted. Also omitted from disease burden calculations are possible adverse effects of cholera during pregnancy.

PROBABLE VACCINE TARGET POPULATION

In endemic areas, cholera occurs with greatest frequency in children between 2 and 15 years of age and in adult females. Children less than 2 years old have a relatively low incidence of the disease, particularly when breast-fed. Thus, vaccination in infancy would be appropriate, and a suitable vaccine could be incorporated into the World Health Organization Expanded Program on immunization (WHO-EPI).

In areas in which the introduction of cholera is recent (neoepidemic areas), the rates of disease are more uniform across the

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Front Matter (R1-R16)
1. Summary (1-18)
2. Priority Setting for Health-Related Investments: A Review of Methods (19-29)
3. Overview of the Analytic Approach (30-43)
4. Comparison of Disease Burdens (44-62)
5. Predictions of Vaccine Development (63-75)
6. Assessing the Likely Utilization of New Vaccines (76-81)
7. Calculation and Comparison of the Health Benefits and Differential Costs Associated with Candidate Vaccines (82-105)
8. Additional Issues in the Selection of Priorities for Accelerated Vaccine Development (106-120)
9. Findings, Conclusions, and Recommendations (121-142)
Appendix A: Selection of Vaccine Candidates for Accelerated Development (143-148)
Appendix B: The Burden of Disease Resulting from Acute Respiratory Illness (149-158)
Appendix C: The Burden of Disease Resulting from Diarrhea (159-169)
Appendix D-1: The Prospects for Immunizing Against Dengue Virus (170-177)
Appendix D-2: The Prospects for Immunizing Against Escherichia coli (178-185)
Appendix D-3: The Prospects for Immunizing Against Hemophilus influenzae Type b (186-196)
Appendix D-4: The Prospects for Immunizing Against Hepatitis A Virus (197-207)
Appendix D-5: The Prospects for Immunizing Against Hepatitis B Virus (208-222)
Appendix D-6: The Prospects for Immunizing Against Japanese Encephalitis Virus (223-240)
Appendix D-7: The Prospects for Immunizing Against Mycobacterium leprae (241-250)
Appendix D-8: The Prospects for Immunizing Against Neisseria meningitidis (251-266)
Appendix D-9: The Prospects for Immunizing Against Parainfluenza Viruses (267-274)
Appendix D-10: The Prospects for Immunizing Against Plasmodium spp. (275-286)
Appendix D-11: The Prospects for Immunizing Against Rabies Virus (287-298)
Appendix D-12: The Prospects for Immunizing Against Respiratory Syncytial Virus (299-307)
Appendix D-13: The Prospects for Immunizing Against Rotavirus (308-318)
Appendix D-14: The Prospects for Immunizing Against Salmonella typhi (319-328)
Appendix D-15: The Prospects for Immunizing Against Shigella spp. (329-337)
Appendix D-16: The Prospects for Immunizing Against Streptococcus Group A (338-356)
Appendix D-17: The Prospects for Immunizing Against Streptococcus pneumoniae (357-375)
Appendix D-18: The Prospects for Immunizing Against Vibrio cholerae (376-389)
Appendix D-19: The Prospects for Immunizing Against Yellow Fever (390-402)
Appendix E: Questionnaire for Assessing Morbidity-Mortality Trade-Offs (403-411)
Appendix F: Technical Notes (412-412)
Appendix G: Biographical Notes on Committee Members (413-417)
Appendix H: Additional Sources of Advice to the Committee (418-419)
Appendix I: Contents of Supplement to Volume II (420-420)
Appendix J: Preface to Volume I (421-422)
Appendix K: Contents to Volume I (423-423)
Index (424-432)