Pathobiology of HIV in the Human Monocyte-Macrophage.

Abstract

In the past year, we have made considerable progress in addressing specific aims of our proposal. We have studied the interaction of HIV with monocyte-macrophages and compared these interactions with those that occur in human T lymphocytes. We have determined that human kit ligand/stem cell factor, a newly identified cytokine elaborated by mesenchymal cells, does not up-regulate HIV infection in monocyte-macrophages and is capable of protecting hematopoietic progenitors from a number of suppressive cytokines and drugs. Human interleukin-3 was found to be less active in protecting similar populations of cells and is known to up-regulate HIV, making the kit ligand/stem cell factor a cytokine whose therapeutic potential should be further explored in the context of AIDS. We have also pursued the regulation of HIV expression by steroid hormone receptors. It appears that there is a responsive element in the negative regulatory element (NRE) of many, but not all, HIV isolates which bind homodimers and heterodimers of different steroid hormone receptor proteins. The response of monocytes to physiological ligands such as retinoids, with respect to modulation of HIV infection, is under investigation.

Document Details

Document Type
Technical Report
Publication Date
Oct 13, 1992
Accession Number
ADA258586

Entities

People

  • Jerome E. Groopman

Organizations

  • Beth Israel Deaconess Medical Center

Tags

DTIC Thesaurus Topics

  • Blood
  • Cardiovascular System
  • Cells
  • Cytokines
  • Hiv Infections
  • Infection
  • Lymphocytes
  • Macrophages
  • Monocytes
  • Proteins
  • Stem Cells
  • T Lymphocytes
  • Wound Infections

Fields of Study

  • Medicine

Readers

  • Breast cancer cell signaling and growth regulation.
  • Immunology
  • Theoretical Analysis.

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech