Medical Journals

Early Depletion of Proliferating B Cells of Germinal Center in Rapidly Progressive Simian Immunodeficiency Virus Infection.

Authors:
  • Zhang Zhi-Qiang
  • Casimiro Danilo R
  • Schleif William A
  • Chen Minchun
  • Citron Michael
  • Davies Mary-Ellen
  • Burns Janine
  • Liang Xiaoping
  • Fu Tong-Ming
  • Handt Larry
  • Emini Emilio A
  • Shiver John W

From: Department of Vaccines and Biologics Research, Merck Research Laboratories, West Point, PA 19486, USA. zhiqiang_zhang@merck.com

Virology

  • Publish Date: May 2007
  • ISSN: 0042-6822
  • Volume: 361
  • Issue: 2
  • Pages: 455-64
  • Medium: Print
  • Language: English
  • Citation (JAMA): Zhang Zhi-Qiang, Casimiro Danilo R, Schleif William A, et al. Early Depletion of Proliferating B Cells of Germinal Center in Rapidly Progressive Simian Immunodeficiency Virus Infection.. Virology May 2007;361:455-64

Abstract

Lack of virus specific antibody response is commonly observed in both HIV-1-infected humans and SIV-infected monkeys with rapid disease progression. However, the mechanisms underlying this important observation still remain unclear. In a titration study of a SIVmac239 viral stock, three out of six animals with viral inoculation rapidly progressed to AIDS within 5 months. Unexpectedly, there was no obvious depletion of CD4(+) T cells in both peripheral and lymph node (LN) compartments in these animals. Instead, progressive depletion of proliferating B cells and disruption of the follicular dendritic cell (FDC) network in germinal centers (GC) was evident in the samples collected at as early as 20 days after viral challenge. This coincided with undetectable, or weak and transient, virus-specific antibody responses over the course of infection. In situ hybridization of SIV RNA in the LN samples revealed a high frequency of SIV productively infected cells and large amounts of accumulated viral RNA in the GCs in these animals. Early severe depletion of GC proliferating B cells and disruption of the FDC network may thus result in an inability to mount a virus-specific antibody response in rapid progressors, which has been shown to contribute to accelerated disease progression of SIV infection.

Mesh Headings (Keywords): Animals, Antibodies, Viral, B-Lymphocytes, Biopsy, Cell Count, Disease Progression, Germinal Center, Hyperplasia, Lymph Nodes, Macaca mulatta, Male, Simian Acquired Immunodeficiency Syndrome, Simian immunodeficiency virus, Viral Load


Check for Full Text / PubMed Unique Identifier (PMID): 17223151


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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