Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1975 Apr;11(4):737-41.
doi: 10.1128/iai.11.4.737-741.1975.

Multiple sclerosis-induced reduction in the yield of a mouse cell line

Multiple sclerosis-induced reduction in the yield of a mouse cell line

R I Carp et al. Infect Immun. 1975 Apr.

Abstract

Cultures of a mouse cell line (PAM) were treated with 71 multiple sclerosis (MS) and 45 non-MS samples. Of the cultures treated with MS material, 80 percent (58) showed a reduction in cell yield (compared to untreated controls) of at least 20 percent by the third passage after inoculation. The MS samples were from 40 MS cases, and a total of 36 cases yielded at least one positive sample. The agent responsible for the decrease was not limited to nervous tissue, but was also found in serum, cerebrospinal fluid, spleen, kidney, and lymph node of MS patients. Positive samples were present at every stage of the disease. None of the non-MS samples yielded cell counts significantly different from untreated controls. The non-MS category included 12 samples from healthy individuals, 13 assorted non-central nervous system disease samples, and the following central nervous system disease samples: six subacute sclerosing panencephalitis, three Huntington's chorea, two Parkinsonism, six amyotrophic lateral sclerosis, one stroke, one encephalopathy, and one epilepsy. Brain homogenates from mice inoculated with MS tissues elicited the decrease, whereas brain homogenates from mice inoculated with non-MS samples did not.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Proc Soc Exp Biol Med. 1962 Dec;111:562-6 - PubMed
    1. Proc R Soc Med. 1968 Sep;61(9):937-40 - PubMed
    1. Lancet. 1973 Jun 23;1(7817):1415-7 - PubMed
    1. Lancet. 1972 Aug 5;2(7771):280-1 - PubMed
    1. Acta Neuropathol. 1973;25(4):281-90 - PubMed

Substances

LinkOut - more resources