Immunoglobulins for Prophylaxis or Treatment of Infectious Diseases

Article information

J Korean Med Assoc. 2008;51(12):1151-1157
Publication date (electronic) : 2008 December 31
doi : https://doi.org/10.5124/jkma.2008.51.12.1151
Department of Pediatrics, Ewha Womans University College of Medicine, Korea. kaykim@ewha.ac.kr

Abstract

Administration of antibodies as a passive immunization is indicated for the replacement of deficiencies, prophylaxis or amelioration of infectious diseases for susceptible individuals and those at high risk for complications of infections. Antibodies can be administered either as human or animal plasma or serum, as pooled human immunoglobulin (IG) for intravenous or intramuscular use, as high-titer human IG from immunized or convalescing donors, or as monoclonal antibodies. Immunoglobulins are widely used for prevention of hepatitis A and measles and specific immunoglobulins are used for prevention of hepatitis B, tetanus, rabies, and varicella in susceptible people. A humanized murine monoclonal antibodies against respiratory syncytial virus have been licensed. This paper reviews the current use and recommendation of antibody products for the prevention and treatment of infectious diseases.

References

1. Pickering LK, Baker CJ, Long SS, McMillan JA, eds. American Academy of Pediatrics. Passive immunization. 2006 Red book: Report of the Committee on infectious diseases 2006. 27th edth ed. Elk Grove Village, IL: American Academy of Pediatrics; 54–66.
2. American Academy of Pediatrics Committee on Infectious Diseases. Committee on Fetus and Newborn. Revised indications for the use of palivizumab and respiratory syncytial virus immune globulin intravenous for the prevention of respiratory syncytial virus infections. Pediatrics 2003. 1121442–1446.
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Article information Continued

Table 1

Efficacy of antibody in the prevention and treatment of infectious diseases

Table 1

Table 2

Guideline of tetanus prophylaxis in wound management

Table 2

*wounds contaminated with dirt, feces, soil, and saliva; puncture wounds; avulsions; wounds resulting from missiles, crushing, burns, and frostbite

Yes, if ≧ 10 years last tetanus-containing dose

Yes, if ≧ 5 years last tetanus-containing dose

Table 3

Indications for post-exposure immunoprophylaxis of hepatitis B virus infection

Table 3

Table 4

Indications for post-exposure immunoprophylaxis of varicella zoster virus infection

Table 4

Table 5

Recommended intervals between immunoglobulin administration and MMR immunization

Table 5