Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 May;10(3):129-34.
doi: 10.1097/COH.0000000000000154.

History of passive antibody administration for prevention and treatment of infectious diseases

Affiliations
Review

History of passive antibody administration for prevention and treatment of infectious diseases

Barney S Graham et al. Curr Opin HIV AIDS. 2015 May.

Abstract

Purpose of review: We describe the history of passive immunization to provide context for the series of articles to follow. The history of passive immunization with antibodies to prevent or treat infectious diseases is a story of different eras. There was an extraordinary era of discovery and clinical implementation before the chemical nature of antibodies was even known. This empirical process provided the resources and reagents used to describe and characterize humoral immunity, better define the chemical properties and structure of antibodies, and extend the clinical use of immunoglobulin products to treat or prevent multiple viral and bacterial diseases over the ensuing several decades. The next distinct era came with the discovery of processes to produce monoclonal antibodies (mAbs), and development of more specific therapies. Interestingly, mAb technology resulted in many products to treat autoimmune and allergic diseases, but only one common infectious disease, respiratory syncytial virus, and only in a restricted population of high-risk infants.

Recent findings: The current era began in 2003 with a series of publications demonstrating processes for rapidly producing human mAbs.

Summary: This technology combined with new sequencing technology, advances in structural biology, atomic-level molecular design, and increased capacity for synthetic biology, promises new opportunities to apply passive immunization to the prevention and treatment of infectious diseases.

PubMed Disclaimer

Conflict of interest statement

Conflicts of interest: Dr. Ambrosino is an inventor on patents involving monoclonal antibodies for rabies and C. difficile toxin. The remaining author has no conflicts of interest.

Figures

Fig 1
Fig 1. Collection of blood for production of anti-diphtheria horse serum
Jin was the horse associated with the deaths of 13 children treated with immune serum collected near the time of his death from tetanus in 1901. The 1902 Biologics Control Act established standards for the processing and labeling of biological products for human use. Source: National Archives and Records Administration

References

    1. Winau F, Winau R. Emil von Behring and serum therapy. Microbes and infection / Institut Pasteur. 2002;4(2):185–8. - PubMed
    1. Lindenmann J. Origin of the terms ‘antibody’ and ‘antigen’. Scandinavian Journal of Immunology. 1984;19(4):281–5. - PubMed
    1. Ramon G. Sur l'augmentation anormale de l'antitoxine chez les chevaux producteurs de serum antidiptherique. Bull Soc Centr Med Vet. 1925;101:227.
    1. Luke TC, Kilbane EM, Jackson JL, Hoffman SL. Meta-analysis: convalescent blood products for Spanish influenza pneumonia: a future H5N1 treatment? Annals of Internal Medicine. 2006;145(8):599–609. - PubMed
    1. Janeway CA. Use of concentrated human gamma globulin in the prevention and attenuation of measles. Bull NY Acad Med. 1945;21:202–2. - PMC - PubMed

Publication types

MeSH terms

Substances