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Journal of Virology, December 1998, p. 9421-9427, Vol. 72, No. 12
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Modulation of Immune System Function by Measles Virus Infection:
Role of Soluble Factor and Direct Infection
Robert S.
Fujinami,1,*
Xinmin
Sun,1
Joseph M.
Howell,1
James C.
Jenkin,2 and
James B.
Burns1,3
Department of
Neurology1 and
Department of
Hematology,2 University of Utah School of
Medicine, Salt Lake City, Utah 84132, and
Veterans Affairs
Medical Center, Salt Lake City, Utah 841483
Received 13 April 1998/Accepted 27 August 1998
Measles virus infection can result in a variety of immunologic
defects. We have begun studies to determine the basis for the lack of
immune responsiveness to antigen and mitogen following infection. Here
we present data showing that Epstein-Barr virus-transformed B-cell
lines infected with measles virus produce a soluble factor that can
inhibit antigen-specific T-cell proliferation and inhibit the
proliferation of uninfected B cells. The soluble factor was neither
interleukin-10, transforming growth factor
, nor alpha/beta interferon. B cells infected with measles virus or treated with the
soluble factor were unable to present antigen to T cells in a manner
that supported antigen-specific proliferation. This could represent one
mechanism of how measles virus limits T-cell expansion. However, we
found that once CD4+ or CD8+ T cells were
activated, their cytolytic activity was intact whether infected with
measles virus or treated with soluble factor. Thus, while slow to be
generated these cytoxic cells could participate in viral clearance.
*
Corresponding author. Mailing address: Department of
Neurology, University of Utah, 50 North Medical Dr., Salt Lake City, UT
84132. Phone: (801) 585-3305. Fax: (801) 585-3311. E-mail: Robert.Fujinami{at}hsc.utah.edu.
Journal of Virology, December 1998, p. 9421-9427, Vol. 72, No. 12
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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