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US4595588A Expired / Lapsed US ⏱️ 0.0 years remaining

Natural inhibitor that protects against viral infections

Assignee: The University of Texas System
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Filing: 1984-05-24
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Granted: 1986-06-17
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Expires: 2004-05-24
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Abstract

Abstract A treatment and prophylaxis of viral infections in mammals is provided. The method involves administering an amount of a contact-blocking viral inhibitor (CVI) sufficient to elevate the concentration of the viral inhibitor in the mammal's tissue above the naturally occurring concentration in that same tissue. Methods for purifying and concentrating CVI are presented. The cellular viral inhibitor is characterized by broad antiviral activity, potency, reversible inhibition of viral attachment, cross species activity and molecular size. Natural levels of CVI range from 6 U/0.1 ml in tears to 400 U/0.1 ml in gastric secretions, with titers between these ranges found in colostrum, milk, plasma, saliva and urine. Biochemical characterization of the CVI indicates that it resists denaturation by heat, acid and alkali, and it exhibits a molecular size on the order of 2500 daltons.

Inventors

  • 👤 Samuel Baron
  • 👤 M. Louese McKerlie

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 09:37
CPC Classifications
A; A61; A61K; A61K35/00; A61K35/12; A61K35/13; A61K35/48; A61K35/54; A61P; A61P31/00; A61P31/12; C; C12; C12N; C12N1/00; C12P; C12P1/00; C12R; C12R2001/00; C12R2001/91; Y; Y02; Y02A; Y02A50/00; Y02A50/30; Y10; Y10S; Y10S435/00; Y10S435/8215; Y10S435/948

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 164 words
A method for treating a mammal infected with a virus comprising administering to the mammal an antiviral composition comprising a therapeutically effective amount of cellular viral inhibitor having the characteristics of (a) lacking species specificity in that the cellular viral inhibitor obtained from one species cell or tissue source is active in heterologous cells or tissue, (b) broad antiviral activity against a number of different viruses including vaccinia virus, polio virus type I, herpes simplex virus, sindbis virus, mengo virus, influenza virus, and vesicular stomatitis virus, (c) an apparent molecular mass ranging from about 2500 to 3000 daltons as determined by gel filtration chromatography, (d) temperature stability between 100° C. and 4° C., (e) stable between pH 1 and 13 and (f) produced spontaneously in tissue absent viral infection; together with a pharmaceutically diluent, said administered amount of the cellular viral inhibitor sufficient to elevate the concentration of said cellular viral inhibitor in the mammal's virally infected tissue above the naturally occurring concentration therein.
Claim 2
Independent Claim 164 words
A method for treating a mammal infected with a virus comprising administering to the mammal an antiviral composition comprising a therapeutically effective amount of cellular viral inhibitor having the characteristics of (a) lacking species specificity in that the cellular viral inhibitor obtained from one species cell or tissue source is active in heterologous cells or tissue, (b) broad antiviral activity against a number of different viruses including vaccinia virus, polio virus type I, herpes simplex virus, sindbis virus, mengo virus, influenza virus, and vesicular stomatitis virus, (c) an apparent molecular mass ranging from about 2500 to 3000 daltons as determined by gel filtration chromatography, (d) temperature stability between 100° C. and 4° C., (e) stable between pH 1 and 13 and (f) produced spontaneously in tissue absent viral infection; together with a pharmaceutically diluent, said administered amount of the cellular viral inhibitor sufficient to elevate the concentration of said cellular viral inhibitor in the mammal's virally infected tissue above the naturally occurring concentration therein.
Claim 3
Dependent Claim 32 words
A method according to claim 1 wherein the concentration of cellular viral inhibitor in the mammal's tissue is elevated to a concentration that is 5-10 fold higher than that naturally occurring therein.
Claim 4
Dependent Claim 37 words
The method according to claim 1 wherein the viral infection is influenza virus (ortho myxoviruses), Semliki Forest virus (togaviruses), vesicular stomatitis virus (rhabdoviruses), polio virus and mengovirus (picornaviruses), vaccinia virus (poxviruses), and herpes simplex virus (herpes viruses).
Claim 5
Independent Claim 160 words
A method of prophylaxis against viral disease in mammals comprising administering to the mammal an antiviral composition comprising a prophylactically effective amount of cellular viral inhibitor having the characteristics of (a) lacking species specificity in that the cellular viral inhibitor obtained from one species cell or tissue source is active in heterologous cells or tissue, (b) broad antiviral activity against a number of different viruses including vaccinia virus, polio virus type I, herpes simplex virus, sindbis virus, mengo virus, influenza virus, and vesicular stomatitis virus, (c) an apparent molecular mass ranging from about 2500 to 3000 daltons as determined by gel filtration chromatography, (d) temperature stability between 100° and 4° C., (e) stable between pH 1 and 13 and (f) produced spontaneously in tissue absent viral infection; together with a pharmaceutically acceptable diluent, said administered amount of the cellular viral inhibitor sufficient to elevate the concentration of the cellular viral inhibitor above the naturally occurring concentration thereof in said mammal.
Claim 6
Independent Claim 160 words
A method of prophylaxis against viral disease in mammals comprising administering to the mammal an antiviral composition comprising a prophylactically effective amount of cellular viral inhibitor having the characteristics of (a) lacking species specificity in that the cellular viral inhibitor obtained from one species cell or tissue source is active in heterologous cells or tissue, (b) broad antiviral activity against a number of different viruses including vaccinia virus, polio virus type I, herpes simplex virus, sindbis virus, mengo virus, influenza virus, and vesicular stomatitis virus, (c) an apparent molecular mass ranging from about 2500 to 3000 daltons as determined by gel filtration chromatography, (d) temperature stability between 100° and 4° C., (e) stable between pH 1 and 13 and (f) produced spontaneously in tissue absent viral infection; together with a pharmaceutically acceptable diluent, said administered amount of the cellular viral inhibitor sufficient to elevate the concentration of the cellular viral inhibitor above the naturally occurring concentration thereof in said mammal.
Claim 7
Dependent Claim 32 words
A method according to claim 4 wherein the concentration of cellular viral inhibitor in the mammal's tissue is elevated to a concentration that is 5-10 fold higher than that naturally occurring therein.
Claim 8
Dependent Claim 35 words
The method according to claim 4 wherein the viral infection is influenza (orthomyxoviruses), Semliki Forest virus (togaviruses), vesicular stomatitis virus (rhabdoviruses), polio virus and mengovirus (picornaviruses), vaccinia virus (poxviruses), and herpes simplex virus (herpes viruses).
Claim 9
Dependent Claim 14 words
The method of claim 1 wherein the antiviral composition is administered intraperitoneally or intranasally.
Claim 10
Dependent Claim 14 words
The method of claim 4 wherein the antiviral composition is administered intraperitoneally or intranasally.

References Cited (Backward Citations)

US4278662A Cited
US4452734A Cited
US4315914A Cited
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US4508708A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-06-16 1989-12-16 1990-06-17 $2000.00 Window Closed / Lapsed
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