Vaccine, method for its preparation, and use thereof in vaccinating humans against rotavirus infection
AssigneeThe Wistar Institute of Anatomy and Biology
InventorsStanley A. Plotkin, H. Fred Clark
Life of this patent
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Abstract
A live rotavirus vaccine against bovine and human rotaviruses comprising a strain of live bovine rotavirus which does not hemagglutinate primate red blood cells, gives at least about 20 fold higher titers when neutralized with antiserum therefor as compared to heterologous bovine or primate rotaviruses, and has a migration pattern of its RNA genome segments when determined by PAGE substantially as shown by lane WC3 in FIG. 1, the strain of bovine rotavirus having been serially passaged in primate kidney tissue culture a sufficient number of times that when administered to humans the vaccine is immunogenic without causing disease.
Claims17
A method of producing a live rotavirus vaccine against bovine and human rotaviruses, including human serotype 3, which comprises inoculating onto monkey kidney cell culture a strain of live bovine rotavirus which does not hemagglutinate primate red blood cells, gives at least about 20 fold higher titers when neutralized with antiserum therefor as compared to heterologus bovine and primate rotaviruses, and has a migration pattern for its RNA genome segments when determined by PAGE substantially as shown by lane WC3 in FIG. 1, to prepare a seed batch of said virus strain serially passaging virus from said seed batch on cells of the cell line CV-1 (ATCC CCL 70), subjecting said passaged virus to plaque purification on cells of the cell line MA-104, further passaging said plaque-purified virus on cells of the cell line CV-1 (ATCC CCL 70), and harvesting the resulting vaccine from disrupted cells obtained from said last passage, the total number of passages being from about 5 to about 25 and being such that when administered to humans the vaccine is immunogenic without causing disease.
A method of producing a live rotavirus vaccine against bovine and human rotaviruses, including human serotype 3, which when administered to humans is immunogenic without causing disease, which comprises inoculating onto primary Cercopithecus monkey kidney cell culture a strain of live bovine rotavirus which does not hemagglutinate primate red blood cells, gives at least about 20 fold higher titers when neutralized with antiserum therefor as compared to heterologus bovine and primate rotaviruses, and has a migration pattern for its RNA genome segments when determined by PAGE substantially as shown by lane WC3 in FIG. 1, said strain of rotavirus comprising the isolate designated WC 3 (ATCC VR 2101), to prepare a seed batch of said virus strain, serially passaging virus from said seed batch three times on cells of the cell line CV-1 (ATCC CCL 70), subjecting said passaged virus to two successive plaque purifications on cells of the cell line MA-104, further passaging said plaque-purified virus six times on cells of the cell line CV-1 (ATCC CLL 70) and harvesting the resulting vaccine from disrupted cells obtained from the last passage.
A live rotavirus vaccine against bovine and human rotaviruses, including human serotype 3, which when administered to humans is immunogenic without causing disease, comprising a strain of live bovine rotavirus which does not hemagglutinate primate red blood cells, gives at least about 20 fold higher titers when neutralized with antiserum therefor as compared to heterologous bovine or primate rotaviruses, and has a migration pattern of its RNA genome segments when determined by PAGE substantially as shown by lane WC3 in FIG. 1, said strain of rotavirus having been inoculated onto monkey kidney cell culture to prepare a seed batch of said virus strain, virus from said seed batch having been serially passaged on cells of cell line CV-1 (ATCC CCL 70), subjected to plaque purification on cells of cell line MA-104, then serially passaged on cells of the cell line CV-1 (ACC CCL 70), the total nunber of passages being from about 5 to about 25, and the resulting vaccine having been harvested from disrupted cells from the last passage.
A live rotavirus vaccine against bovine and human rotaviruses, including human serotype 3, which when administered to humans is immunogenic without causing disease, comprising a strain of live bovine rotavirus which does not hemagglutinate primate red blood cells, gives at least about 20 fold higher titers when neutralized with antiserum therefor as compared to heterologous bovine or primate rotaviruses, and has a migration pattern of its RNA genome segments when determined by PAGE substantially as shown by lane WC3 in FIG. 1, said strain of rotavirus comprising the isolate designated WC 3 (ATCC VR 2101), and said strain of rotavirus having been inoculated onto primary Cercopithecus kidney cell culture to prepare a seed batch of said virus strain, virus from said seed batch having been serially passaged three times on cells of cell line CV-1 (ATCC CCL 70), subjected to two successive plaque purifications on cells of cell line MA-104, then serially passaged six times on cells of the cell line CV-1 (ACC CCL 70), and the resulting vaccine having been harvested from disrupted cells from the last passage.
A method of vaccinating human beings against bovine and human rotavirus infection comprising administering by oral or nasal route to human beings at least one dose comprising about 10.sup.7 pfu of a live rotavirus vaccine comprising a strain of live rotavirus which does not hemagglutinate primate red blood cells, gives at least about 20 fold higher titers when neutralized with antiserum therefor as compared to heterologous bovine or primate rotaviruses, and has a migration pattern of its RNA genome segments when determined by PAGE substantially as shown by lane WC3 in FIG. 1, said strain of rotavirus comprising the isolate designated WC 3 (ATCC VR 2101), and said strain of rotavirus having been inoculated onto primary Cercopithecus kidney cell culture to prepare a seed batch of said virus strain, virus from said seed batch having been serially passaged three times on cells of cell line CV-1 (ATCC CCL 70), subjected to two successive plaque purifications on cells of cell line MA-104, then serially passaged six times on cells of the cell line CV-1 (ACC CCL 70), and the resulting vaccine having been harvested from disrupted cells from the last passage.
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