Literature DB >> 3631680

Past, present, and future immunotherapy of snake venom poisoning.

J B Sullivan.   

Abstract

Management of snake venom poisoning with antivenin has been the time-proven and medically accepted standard in virtually every country, including the United States. All antivenins are equine in source, and administration to patients exposes them to all the adverse effects of heterologous antisera. The purity and specificity of neutralizing antibody titers in antivenin products vary among manufacturers. Research in the early 1980s demonstrated that immunosorbent affinity chromatography could purify a highly specific IgG(T) from equine hyperimmune antisera. This IgG(T) provided superior efficacy and reduced adverse effects as compared to commercial antivenin. The advent of newer biotechnical processes has now opened the doors for novel antibody and antibody fragment treatment of snake venom poisoning.

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Year:  1987        PMID: 3631680     DOI: 10.1016/s0196-0644(87)80737-0

Source DB:  PubMed          Journal:  Ann Emerg Med        ISSN: 0196-0644            Impact factor:   5.721


  5 in total

Review 1.  Antivenom therapy in the Americas.

Authors:  K Heard; G F O'Malley; R C Dart
Journal:  Drugs       Date:  1999-07       Impact factor: 9.546

Review 2.  Snake envenomation. Incidence, clinical presentation and management.

Authors:  B K Nelson
Journal:  Med Toxicol Adverse Drug Exp       Date:  1989 Jan-Feb

Review 3.  Rattlesnake bites in southern California and rationale for recommended treatment.

Authors:  W A Wingert; L Chan
Journal:  West J Med       Date:  1988-01

4.  A human monoclonal immunoglobulin M reduces bacteremia and inflammation in a mouse model of systemic pneumococcal infection.

Authors:  Kevin Fabrizio; Abraham Groner; Marianne Boes; Liise-anne Pirofski
Journal:  Clin Vaccine Immunol       Date:  2007-02-14

5.  Predicting the effects of 8C2, a monoclonal anti-topotecan antibody, on plasma and tissue disposition of topotecan.

Authors:  Dhaval K Shah; Joseph P Balthasar
Journal:  J Pharmacokinet Pharmacodyn       Date:  2013-12-25       Impact factor: 2.745

  5 in total

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