MONOCYTE FUNCTION IN RHESUS MONKEYS WITH SIMIAN ACQUIRED IMMUNE DEFICIENCY SYNDROME NLM AIDSLINE Important note: Information in this article was accurate in 1987. The state of the art may have changed since the publication date.

Click here to return to AIDSLINE main menu
DonateNow
Print this Article


MONOCYTE FUNCTION IN RHESUS MONKEYS WITH SIMIAN ACQUIRED IMMUNE DEFICIENCY SYNDROME

Diss Abstr Int (Sci); 46(7):2255 1986. Unique Identifier : AIDSLINE ICDB/87632301
Legrand EK; Univ. of California, Davis, CA


Abstract: Monocyte function in rhesus monkeys with simian acquired immune deficiency syndrome (SAIDS) was compared with that in age-matched normal juvenile rhesus monkeys. The functional tests were (1) chemotaxis, (2) phagocytosis of opsonized Candida albicans, (3) killing and/or growth inhibition of Candida albicans, (4) generation of respiratory burst (using image analysis to quantitate a nitroblue tetrazolium slide test), (5) growth in culture, and (6) response (morphology and/or respiratory burst) to various stimulating agents such as lymphokines, gamma interferon, endotoxin, and phorbol myristate acetate. The monkeys tested were classified as having either clinical SAIDS (those having lymphadenopathy, splenomegaly, and lymphopenia or neutropenia) or as terminal SAIDS (moribund due to the disease). The responses of the monocytes from the monkeys with clinical SAIDS were indistinguishable from those of normal juvenile rhesus monkeys. However, the monkeys with terminal SAIDS had enhanced phagocytosis and respiratory burst capacity compared to the juvenile controls. Chemotaxis, candidacidal/stasis, and response to stimulating agents were normal in these terminal SAIDS cases. Plasma from the SAIDS monkeys was as capable of opsonizing yeasts and of being able to generate chemotactic factors by endotoxin as was control plasma. SAIDS virus was detected by co-cultivation of pure monocyte-derived macrophage cultures with Raji cells, which form syncytia in the presence of SAIDS virus. Four terminal SAIDS and one late-stage clinical SAIDS were found to be positive when the minimum number of macrophages present in the cultures ranged from less than 50 to about 500. Terminal SAIDS monocyte-derived macrophages in culture as long as 17 days produced SAIDS virus. In three clinical SAIDS cases virus could not be detected when smaller numbers of monocyte-derived macrophages were co-cultured with Raji cells. These data show that in monkeys with SAIDS at least the major effector functions of monocytes and macrophages involved in host defense are intact (even up until death). Additionally, at least some of the monocytes are productively infected and these infected monocytes are viable and adherent in culture.
Keywords: Acquired Immunodeficiency Syndrome/*BLOOD/PHYSIOPATHOLOGY Animal Chemotaxis, Leukocyte Female Macaca mulatta/*BLOOD Male Monocytes/*PHYSIOLOGY Phagocytosis THESIS

KWDacquiredimmunodeficiencysyndrome/KWDblood/physiopathologyanimalchemotaxis,leukocytefemalemacacamulatta/KWDbloodmalemonocytes/KWDphysiologyphagocytosisthesis
870530
M8750343


Copyright © 1987 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

AEGiS is a 501(c)3, not-for-profit, tax-exempt, educational corporation. AEGiS is made possible through unrestricted funding from Boehringer Ingelheim, Bridgestone/Firestone Charitable Trust, Bristol-Myers Squibb Company, Elton John AIDS Foundation, Gill Foundation, the National Library of Medicine, Quest Diagnostics, Roche and Trimeris, and donations from users like you. Always watch for outdated information. This article first appeared in 1987. This material is designed to support, not replace, the relationship that exists between you and your doctor.

AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.

Copyright ©1980, 1987. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content. .