Publication:
Antibody response to suckling mouse brain rabies vaccines for post exposure treatment

dc.contributor.authorPornthep Chanthavanichen_US
dc.contributor.authorPravan Suntharasamaien_US
dc.contributor.authorM. J. Warrellen_US
dc.contributor.authorChaisin Viravanen_US
dc.contributor.authorSornchai Looareesuwanen_US
dc.contributor.authorWichai Supanaranonden_US
dc.contributor.authorJuntra Karbwangen_US
dc.contributor.authorD. A. Warrellen_US
dc.contributor.authorR. E. Phillipsen_US
dc.contributor.authorAbha Sinhasenien_US
dc.contributor.authorPor Boonyarataphanen_US
dc.contributor.authorP. Sureauen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherThai Red Cross Agencyen_US
dc.contributor.otherInstitut Pasteur, Parisen_US
dc.contributor.otherLiverpool School of Tropical Medicineen_US
dc.date.accessioned2018-06-14T09:02:09Z
dc.date.available2018-06-14T09:02:09Z
dc.date.issued1987-01-01en_US
dc.description.abstractA new suckling mouse brain vaccine (SMBV) against rabies, produced by the Thai Red Cross Society, was compared with the well established Institut Pasteur SMBV in patients with very low risk rabies contact. The 4 regimens used were the standard daily injections with booster doses of Thai Red Cross vaccine (TRCV) and Institut Pasteur Vaccine (IPV), and a reduced dose scheme of 6 injections as used for tissue cuture vaccines. The effect of 20 IU/kg of human rabies immune globulin (HRIG) was tested on each regimen, making 8 groups, a total of 122 patients. Blood samples taken on days 0, 7, 14, 28 and 91 were tested for neutralizing antibody. Only the standard IPV regimen produced antibody in every patient; all had levels greater than 0·5 IU at some stage. Two people (13%) given the standard TRCV produced no detectable antibody (≤ 0·1 IU) throughout the study. The reduced dose regimens gave very low antibody levels. 7% of the IPV and 76% of the TRCV groups failed to produce antibody on any occasion. The antibody response was significantly suppressed by the administration of HRIG. Compared to the original South American SMBV, the vaccines tested induced low levels of short lived antibody. No reduction in the dosage of SMBV should be considered unless the potency of the product is adequate. © 1987.en_US
dc.identifier.citationTransactions of the Royal Society of Tropical Medicine and Hygiene. Vol.81, No.2 (1987), 260-263en_US
dc.identifier.doi10.1016/0035-9203(87)90234-3en_US
dc.identifier.issn00359203en_US
dc.identifier.other2-s2.0-0023072764en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/15364
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0023072764&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleAntibody response to suckling mouse brain rabies vaccines for post exposure treatmenten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0023072764&origin=inwarden_US

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