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

被引:94
作者
Graham, Barney S. [1 ]
Ambrosino, Donna M. [2 ]
机构
[1] NIAID, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
[2] CVC, Rockville, MD USA
关键词
antibody; history; immunoglobulin; passive immunization; serum therapy; ARGENTINE HEMORRHAGIC-FEVER; SOLUBLE SPECIFIC SUBSTANCE; B-CELLS; NEUTRALIZING ANTIBODIES; MONOCLONAL-ANTIBODIES; IMMUNE PLASMA; SERUM THERAPY; PNEUMOCOCCUS; VIRUS; ANTIGEN;
D O I
10.1097/COH.0000000000000154
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:129 / 134
页数:6
相关论文
共 29 条
[1]   HEMOPHILUS INFLUENZAE MENINGITIS TREATED WITH STREPTOMYCIN [J].
ALEXANDER, HE ;
RAKE, G ;
DONOVICK, R .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1946, 132 (08) :434-440
[2]   Maintenance of serological memory by polyclonal activation of human memory B cells [J].
Bernasconi, NL ;
Traggiai, E ;
Lanzavecchia, A .
SCIENCE, 2002, 298 (5601) :2199-2202
[3]   SERUM THERAPY REVISITED - ANIMAL-MODELS OF INFECTION AND DEVELOPMENT OF PASSIVE ANTIBODY THERAPY [J].
CASADEVALL, A ;
SCHARFF, MD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (08) :1695-1702
[4]  
Connor E, 1997, PEDIATRICS, V99, P93
[5]   IMPORTANCE OF DOSE OF NEUTRALIZING ANTIBODIES IN TREATMENT OF ARGENTINE HEMORRHAGIC-FEVER WITH IMMUNE PLASMA [J].
ENRIA, DA ;
BRIGGILER, AM ;
FERNANDEZ, NJ ;
LEVIS, SC ;
MAIZTEGUI, JI .
LANCET, 1984, 2 (8397) :255-256
[6]   ANTIVIRAL TREATMENT OF ARGENTINE HEMORRHAGIC-FEVER [J].
ENRIA, DA ;
MAIZTEGUI, JI .
ANTIVIRAL RESEARCH, 1994, 23 (01) :23-31
[7]   Treatment of Argentine hemorrhagic fever [J].
Enria, Delia A. ;
Briggiler, Ana M. ;
Sanchez, Zaida .
ANTIVIRAL RESEARCH, 2008, 78 (01) :132-139
[8]  
GREENMAN L, 1994, NEW STATESMAN SOC, V7, P13, DOI 10.1038/ng0594-13
[9]  
HAMMON WM, 1953, JAMA-J AM MED ASSOC, V151, P1272
[10]   A quantitative study of the precipitin reaction between type III Pneumococcus polysaccharide and purified homologous antibody [J].
Heidelberger, M ;
Kendall, FE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1929, 50 (06) :809-823