Polarized type 1 cytokine response and cell-mediated immunity determine genetic resistance to mousepox

Date

2004

Authors

Chaudhri, Geeta
Panchanathan, Vijay
Buller, R. Mark
van den Eertwegh, Alfons
Claassen, E.
Zhou, Jiansheng
De Chazal, Rosalind
Laman, J.
Karupiah, Gunasegaran

Journal Title

Journal ISSN

Volume Title

Publisher

National Academy of Sciences (USA)

Abstract

Ectromelia virus (ECTV), a natural mouse pathogen and an orthopoxvirus, has been used to investigate the correlation between polarized type 1 or type 2 immune responses and resistance to disease in poxvirus infections by using well defined resistant and susceptible mouse strains. Our data show that distinct differences exist in the cytokine profiles expressed in resistant and susceptible mice infected with ECTV. Resistant C57BL/6 mice generate a type 1 cytokine response [IFN-γ, IL-2, and tumor necrosis factor (TNF)], within the first few days of infection, which is associated with strong cytotoxic T lymphocyte response (CTL) and recovery from ECTV infection. Susceptible strains of mice (BALB/c and A/J) on the other hand generate a type 2 cytokine response (IL-4 but little or no IFN-γ and IL-2), which is associated with a weak or an absent CTL response, resulting in uncontrolled virus replication and death. Although deletion of IL-4 function alone did not change the outcome of infection in susceptible mice, the loss of IFN-γ function in resistant mice abrogated natural killer (NK) cell and CTL effector functions resulting in fulminant disease and 100% mortality. Therefore, a clear link exists between the early production of specific type 1 cytokines, in particular, IFN-γ, the nature of the cellular immune response, and disease outcome in this virus model. This finding in the mousepox model raises the possibility that inappropriate cytokine responses may result in increased susceptibility to smallpox in humans.

Description

Keywords

cytokine, gamma interferon, interleukin 2, interleukin 4, tumor necrosis factor, adolescent, animal cell, animal model, cellular immunity, cytokine production, cytotoxic T lymphocyte, disease course, Ectromelia virus, female, genetic resistance

Citation

Source

PNAS - Proceedings of the National Academy of Sciences of the United States of America

Type

Journal article

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Restricted until

2037-12-31