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PMID: 19870474 Published · ppublish English Journal Article

ACTIVE IMMUNICATION OF GUINEA PIGS WITH THE VIRUS OF EQUINE ENCEPHALOMYELITIS : I. QUANTITATIVE EXPERIMENTS WITH VARIOUS PREPARATIONS OF ACTIVE VIRUS.

The Journal of experimental medicine ·Vol. 63 ·No. 3 ·1936-02-29 ·Pages 311-24

Olitsky PK, Cox HR

Abstract

Active Eastern or Western equine encephalomyelitis virus in three forms,-chemically untreated but simply passaged through series of mice; adsorbed on alumina Gel C, and precipitated by tannin,-yielded practically the same results when employed for the immunization of guinea pigs. The virus is not inactivated by the process of adsorption or precipitation : guinea pigs and mice inoculated in the brain with these materials develop lethal encephalomyelitis in the same manner as when chemically untreated mouse passage virus has been used. Moreover, there is no difference in the rate of absorption in vivoof the chemically treated and untreated virus preparations. After storage of the three immunizing preparations-the longest periods thus far studied being 2 to 3 months for mouse passage and for precipitated suspensions, and 6 months for adsorbed material-each was found to contain an amount of virus sufficient to produce immunity in animals against the usual intracerebral test inoculation. Finally, the protection afforded by the three preparations is apparently durable, as is true of many active viruses utilized in preventive treatments. The amount of the virus necessary to confer protection may be defined as that which immunizes (a) with the least number of antigenic units and (b) with the minimum of febrile reaction and blood infection. In proportion as this amount is exceeded, the incidence of fever and of circulating virus increases and, on the other hand, as this amount is decreased, the degree of induced immunity is diminished. We have thus shown that for this particular virus and in the guinea pig, one or two subcutaneous doses of I cc. of any of the different virus preparations, each containing 3 x 10(3) to 3 x 10(4) mouse infective units, bring about protection regularly against experimental infection by way of the nose or subcutis. The results are irregular when the test is made by way of the brain. By three injections, resistance is invariably obtained against as many as 10(3) to 10(4) lethal doses, given intracerebrally. No matter in what form the virus is given, as mouse passage, or adsorbed, or precipitated material, in certain instances fever occurs and virus circulates. With the amount of virus adequate for immunization (3,000 to 30,000 m.i.u.) a mild or subclinical infection may occur in the guinea pig without other manifestation of disease. Lesser quantities of virus apparently fail to gain a foothold in the animal and thus fail to bring about resistance. To conclude, a quantitative basis has been established for the comparison of the immunizing capacities of preparations employed in experimental equine encephalomyelitis in guinea pigs.

Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Olitsky P K
Laboratories of The Rockefeller Institute for Medical Research.
Cox H R
References (5)
5 references, click to expand
  1. THE EFFECTS OF NASALLY INSTILLED VIRUS OF POLIOMYELITIS ON THE CEREBROSPINAL FLUID AND THE BLOOD OF MONKEYS.
    J Exp Med. 1935 Nov 30;62(6):787-804 PMID: 19870448
  2. THE IMMUNOLOGICAL RELATIONSHIP OF EASTERN AND WESTERN STRAINS OF EQUINE ENCEPHALOMYELITIS VIRUS.
    Science. 1933 Dec 22;78(2034):587-8 PMID: 17801697
  3. IMMUNIZATION WITH MIXTURES OF POLIOMYELITIS VIRUS AND ALUMINUM HYDROXIDE.
    J Exp Med. 1931 Feb 28;53(3):399-404 PMID: 19869852
  4. VACCINATION OF MONKEYS AND LABORATORY WORKERS AGAINST PSITTACOSIS.
    J Exp Med. 1934 Jul 31;60(2):211-38 PMID: 19870296
  5. PREVENTION OF EXPERIMENTAL EQUINE ENCEPHALOMYELITIS IN GUINEA PIGS BY MEANS OF VIRUS ADSORBED ON ALUMINUM HYDROXIDE.
    Science. 1934 May 18;79(2055):459 PMID: 17821750
Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1936-02-29
Pages
311-24
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2133342
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