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IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION
Treponema pallida were extracted from rabbit testicular syphilomas and suspended in a special medium in which the organisms remain motile and infectious for several days. On incubation of such suspensions with syphilitic rabbit or human sera and guinea pig complement, the treponemes became non-motil...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1949
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135874/ https://www.ncbi.nlm.nih.gov/pubmed/18113911 |
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author | Nelson, Robert A. Mayer, Manfred M. |
author_facet | Nelson, Robert A. Mayer, Manfred M. |
author_sort | Nelson, Robert A. |
collection | PubMed |
description | Treponema pallida were extracted from rabbit testicular syphilomas and suspended in a special medium in which the organisms remain motile and infectious for several days. On incubation of such suspensions with syphilitic rabbit or human sera and guinea pig complement, the treponemes became non-motile and lost their capacity to infect rabbits. Various factors affecting this immobilization have been investigated. In a preliminary survey of individual sera, immobilizing antibody could be detected in the majority of sera from syphilitic animals and human beings, but was absent in almost all the normal sera examined. It could be demonstrated that the immobilizing and reagin activities of syphilis sera are due to separate antibodies. |
format | Text |
id | pubmed-2135874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1949 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21358742008-04-17 IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION Nelson, Robert A. Mayer, Manfred M. J Exp Med Article Treponema pallida were extracted from rabbit testicular syphilomas and suspended in a special medium in which the organisms remain motile and infectious for several days. On incubation of such suspensions with syphilitic rabbit or human sera and guinea pig complement, the treponemes became non-motile and lost their capacity to infect rabbits. Various factors affecting this immobilization have been investigated. In a preliminary survey of individual sera, immobilizing antibody could be detected in the majority of sera from syphilitic animals and human beings, but was absent in almost all the normal sera examined. It could be demonstrated that the immobilizing and reagin activities of syphilis sera are due to separate antibodies. The Rockefeller University Press 1949-03-31 /pmc/articles/PMC2135874/ /pubmed/18113911 Text en Copyright © Copyright, 1949, by The Rockefeller Institute for Medical Research New York This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Nelson, Robert A. Mayer, Manfred M. IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION |
title | IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION |
title_full | IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION |
title_fullStr | IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION |
title_full_unstemmed | IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION |
title_short | IMMOBILIZATION OF TREPONEMA PALLIDUM IN VITRO BY ANTIBODY PRODUCED IN SYPHILITIC INFECTION |
title_sort | immobilization of treponema pallidum in vitro by antibody produced in syphilitic infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135874/ https://www.ncbi.nlm.nih.gov/pubmed/18113911 |
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