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Vaccines for the 21st Century: A Tool for Decisionmaking (2000)
Institute of Medicine (IOM)

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. "Considerations of Candidate Vaccines." Vaccines for the 21st Century: A Tool for Decisionmaking. Washington, DC: The National Academies Press, 2000.

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Vaccines for the 21st Century: A Tool for Decisionmaking

TABLE 3–1 Candidate Vaccines Included for Full Analysis*

Borrelia burgdorferi

Chlamydia

Coccidioides immites

Cytomegalovirus

Enterotoxigenic E. coli

Epstein-Barr virus

Helicobacter pylori

Hepatitis C virus

Herpes simplex virus

Histoplasma capsulatum

Human papillomavirus

Influenza

Insulin-dependent diabetes mellitus (therapeutic)

Melanoma (therapeutic)

Multiple sclerosis (therapeutic)

Mycobacterium tuberculosis

Neisseria gonorrhea

Neisseria meningitidis B

Parainfluenza

Respiratory syncytial virus

Rheumatoid arthritis (therapeutic)

Rotavirus

Shigella

Streptococcus, group A

Streptococcus, group B

Streptococcus pneumoniae

*Candidate vaccines are preventive unless indicated as (therapeutic).

Insufficient Basic Science Information

The Committee judged that a vaccine approach to control a number of diseases caused by microorganisms was not attainable within the next 20 years. In some instances not enough information was available concerning the antigens that stimulate protective immune response or the host responses necessary to provide protection. In other cases, a class of infectious agents are known to cause disease (e.g., periodontal disease), but the major contributors to disease within that class are not yet identified. In other cases, knowledge of the natural history of the infection was inadequate. Some of these infectious diseases against which vaccines were not yet considered feasible occur in healthy hosts who experience the loss of integrity of the skin or the disruption of normal intestinal barriers to microorganisms, which permits the development of secondary infections (e.g., infections caused by Clostridium perfringens or Bacteroides fragilis). Other diseases are the result of intimate exposure of healthy hosts to others who harbor certain pathogens (e.g., Treponema pallidum and Mycobacte

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Front Matter (R1-R12)
Executive Summary (1-10)
Introduction (11-16)
Progress in Vaccine Development (17-38)
Considerations of Candidate Vaccines (39-52)
Overview of Analytic Approach and Results (53-92)
Review of the Analytical Model (93-108)
Ethical Considerations and Caveats (109-122)
Observations (123-132)
References (133-142)
Appendix 1: Borrelia burgdorferi (143-148)
Appendix 2: Chlamydia (149-158)
Appendix 3: Coccidioides Immitis (159-164)
Appendix 4: Cytomegalovirus (165-172)
Appendix 5: Enterotoxigenic E. coli (173-176)
Appendix 6: Epstein-Barr Virus (177-180)
Appendix 7: Helicobacter pylori (181-188)
Appendix 8: Hepatitis C (189-194)
Appendix 9: Herpes Simplex Virus (195-206)
Appendix 10: Histoplasma capsulatum (207-212)
Appendix 11: Human Paillomavirus (213-222)
Appendix 12: Influenza A and B (223-232)
Appendix 13: Insulin-Dependent Diabetes Mellitus (233-238)
Appendix 14: Melanoma (239-244)
Appendix 15: Multiple Sclerosis (245-250)
Appendix 16: Mycobacterium tuberculosis (251-256)
Appendix 17: Neisseria gonnorrhea (257-266)
Appendix 18: Neisseria meningitidis (267-272)
Appendix 19: Parainfluenza Virus (273-278)
Appendix 20: Respiratory Syncytial Virus (279-284)
Appendix 21: Rheumatoid Arthritis (285-290)
Appendix 22: Rotavirus (291-294)
Appendix 23: Shigella (295-298)
Appendix 24: Streptococcus, Group A (299-304)
Appendix 25: Streptococcus, Group B (305-312)
Appendix 26: Streptococcus pneumoniae (313-322)
Appendix 27: Information on accessing Electronic Spreadsheets (323-324)
Appendix 28: Summary of Workshops (325-434)
Appendix 29: Questions Posed to Outside Experts and List of Responders (435-442)
Index (443-460)