Treatment of the Murine, Retrovirus-Induced Lymphoproliferative Immunodeficiency Disease (LP-BM5) in C57BL/10 Mice with the Immunomodulator Imexon

Carole Y. Funk, Julia Eisman, Evan M. Hersh

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Imexon (4-imino-1, 3-diazabicyclo-(3.1.0)-hexan-2-one) a cyanoaziridine compound was studied in the treatment of the murine retrovirus-induced immunodeficiency disease model of AIDS (LP-BM5, MAIDS). Imexon, in dose-dependent fashion, partially prevented the development of hypergammaglobulinemia and splenomegaly, and partially prevented the decline in the phytohemagglutinin-induced proliferative response of spleen lymphocytes when started 1 or 15 days after virus inoculation. There was a statistically significant reduction in these disease-associated manifestations. When animals were treated starting 78 or 92 days after virus inoculation, lymphadenopathy was completely abrogated and survival was significantly prolonged in a dose-responsive manner. Since Imexon and other cyanoaziridine compounds have been safely administered to humans, we suggest that this class of compounds be further investigated in both large animal models of HIV infection and in patients with HIV-induced disease.

Original languageEnglish (US)
Pages (from-to)633-638
Number of pages6
JournalAIDS Research and Human Retroviruses
Volume8
Issue number5
DOIs
StatePublished - May 1992

ASJC Scopus subject areas

  • Immunology
  • Virology
  • Infectious Diseases

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