Table 1


From the following article

The growth and potential of human antiviral monoclonal antibody therapeutics

Wayne A Marasco & Jianhua Sui

Nature Biotechnology 25, 1421 - 1434 (2007) Published online: 7 December 2007

doi:10.1038/nbt1363

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Table 1. Passive immunotherapy with convalescent human serum

Year of studyDiseaseProphylaxis or treatmentNumber of study subjectsTrend in benefitReference

aOther studies refer to ref. 1.

bImmune BHF gamma globulin was used.

cHIV hyperimmune globulin was used.

1907Measles (Rubeola)ProphylaxisUnknownPrevention.2
1918MeaslesaProphylaxis1One child in a family of four children was given serum from the first infected child and was protected; the other two contracted measles.96
1918MeaslesProphylaxis4Prophylaxis was effective.96
19181918 Pandemic fluTreatment56Early administration generally resulted in distinct improvement in clinical symptoms.9798
1923Varicella-Zoster virusProphylaxis42Seven contracted a mild form of the disease, 35 escaped without symptoms.99
1963bBolivian hemorrhagic feverTreatment4Individuals recovered after 6–8 weeks.100
1959–1983Argentine hemorrhagic feverTreatment4,433Mortality rate of 3.29% (versus 42.85% in individuals treated before convalescent plasma was used).101
1974–1978Argentine hemorrhagic feverTreatment2171.1% mortality rate of those treated with immune plasma.102
1969Lassa feverTreatment1The individual recovered.103
1984Lassa feverProphylaxis and treatment27All study subjects given plasma on or before the 10th day survived with a rapid response to therapy.104
1995Ebola hemorrhagic feverTreatment812.5% fatality rate (versus overall case fatality rate of 80%); inconclusive regarding neutralizing antibodies in convalescent blood.105
1993HIV-1Treatment of stage IV AIDS individuals63Randomized double-blind controlled trial. Study subjects were given 250 ml of HIV-immune plasma every 4 weeks. No significant toxicity and effect were found.106
1995HIV-1Treatment of symptomatic HIV infection86Randomized double-blind controlled trial. Study subjects were given 300 ml of plasma rich in anti-HIV-1 antibody every 14 days for 1 year. Clinical benefit was observed.107
2002cHIV-1Prevention of vertical transmission in Uganda60Phase 1/2 trial showed it is safe, well tolerated and similar pharmacokinetic property as other immunoglobulin products.108
2003SARSTreatment1Fever decreased after administration of convalescent plasma.109
2007Influenza A (H5N1)Treatment1Viral load was reduced after infusion of plasma; the individual recovered.110
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