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Low Levels of Perforin Expression in CD8+T Lymphocyte Granules in Lymphoid Tissue during Acute Human Immunodeficiency Virus Type 1 Infection
Author(s) -
Jan Andersson,
Sabine Kinloch,
Anders Sönnerborg,
Jakob Nilsson,
Thomas E. Fehniger,
AnnaLena Spetz,
Homira Behbahani,
LiEan Goh,
Hugh McDade,
Brian Gazzard,
Hans Stellbrink,
David A. Cooper,
Luc Perrin
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/340124
Subject(s) - granzyme a , perforin , cytotoxic t cell , biology , ctl* , granzyme , granzyme b , cd8 , immunology , immune system , virology , lymphocyte , lymphatic system , biochemistry , in vitro
Human immunodeficiency virus (HIV)-specific cytotoxic T lymphocyte (CTL) responses are detectable shortly after the acute phase of HIV infection, but they cannot control viral replication and prevent development of chronic immune suppression. This article describes a defect in the coexpression of perforin in granzyme A-positive CD8(+) T cells in lymphoid tissue from patients with acute HIV infection and a reduction in the perforin-dependent nuclear translocation of granzyme A. Furthermore, intracellular levels of HIV DNA and RNA found in lymphoid tissue were higher (10-100 times) than those found in blood, and blood samples showed more-coordinated cellular perforin/granzyme A expression. This suggests that mechanisms inhibiting CTL-mediated cytotoxicity are operative in lymphoid tissue early in the course of HIV infection.

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