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Clinical and Diagnostic Laboratory Immunology, 07 1995, 434-438, Vol 2, No. 4
MP Nair, KC Chadha, I Stadler, A Sweet and SA Schwartz
While considerable progress in examining the course of human
immunodeficiency virus (HIV) infection in adults has been made, a better
understanding of the natural history of perinatal HIV infection remains to
be obtained. Dysregulation of the production and functions of various
cytokines, especially the interferons (IFNs), during HIV infections has
been reported. Using an in vitro model system, we examined the effects of
the HIV type 1 envelope protein, gp120 (10, 50, and 100 ng/ml), on gamma
IFN (IFN-gamma) and IFN-alpha production by lymphocytes from neonates and
adults and also examined the potential regulatory effects of gp120 on
phorbol 12-myristate acetate (PMA)- and Sendai virus-induced IFN-gamma and
IFN-alpha production by lymphocytes. PMA at a concentration of 50 ng/ml
plus 50 ng of calcium ionophore A23187 per ml was used to induce IFN-gamma,
while 150 hemagglutinating units of Sendai virus was used to induce
IFN-alpha production. The antiviral activity of both IFN-alpha and
IFN-gamma in leukocyte culture supernatants was assayed on BG-9 cells by a
dye uptake technique using vesicular stomatitis virus as a challenge virus.
Placental cord blood leukocyte (CBL) samples from healthy, term infants and
adult peripheral blood leukocytes (APBL) produced no IFN in response to
gp120. However, CBL produced significantly decreased levels of IFN-gamma
compared with APBL in response to PMA plus ionophore. gp120 significantly
suppressed both Sendai virus-induced IFN-alpha and PMA-induced IFN-gamma
production by both CBL and APBL in a dose-dependent manner. However,
gp120-induced suppression of IFN-alpha and IFN-gamma was significantly
greater with CBL than with APBL.(ABSTRACT TRUNCATED AT 250 WORDS)
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Differential effects of human immunodeficiency virus type 1 envelope protein gp120 on interferon production by mononuclear cells from adults and neonates
Department of Medicine and Microbiology, State University of New York at Buffalo, USA.
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