Previous Article | Next Article ![]()
Journal of Virology, September 2000, p. 7738-7744, Vol. 74, No. 17
Center for Immunization Research, Department
of International Health, Johns Hopkins University, Baltimore,
Maryland 21205
Received 17 March 2000/Accepted 25 May 2000
The developing immune response in the lymph nodes of mice infected
with influenza virus has both Th1- and Th2-type characteristics. Modulation of the interactions between antigen-presenting cells and T
cells is one mechanism that may alter the quality of the immune
response. We have previously shown that the ability of dendritic cells
(DC) to stimulate the proliferation of alloreactive T cells is changed
by influenza virus due to viral neuraminidase (NA) activity. Here we
show that DC infected with influenza virus A/PR/8/34 (PR8) stimulate T
cells to produce different types of cytokines in a dose-dependent
manner. Optimal amounts of the Th1-type cytokines interleukin-2 (IL-2)
and gamma interferon (IFN-
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Polarization of Allogeneic T-Cell Responses by
Influenza Virus-Infected Dendritic Cells
) were produced from T cells stimulated by
DC infected with low doses of PR8, while the Th2-type cytokines IL-4
and IL-10 were produced only in response to DC infected with high doses
of PR8. IL-2 and IFN-
levels corresponded with T-cell proliferation
and were dependent on the activity of viral NA on the DC surface. In
contrast, IL-4 secretion required the treatment of T cells with NA.
Since viral particles were released only from DC that are infected with
high doses of PR8, our results suggest that viral NA on newly formed virus particles desialylates T-cell surface molecules to facilitate a
Th2-type response. These results suggest that the activity of NA may
contribute to the mixed Th-type response observed during influenza
virus infection.
*
Corresponding author. Mailing address: Department of
International Health, Johns Hopkins University, Room 5026, 615 N. Wolfe St., Baltimore, MD 21205-1901. Phone: (410) 614-3407. Fax: (410) 955-7159. E-mail: meichelb{at}jhsph.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»